Variant report

Variant	esv2758656
Chromosome Location	chr16:74334780-74587185
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3162)
CpG islands
(count:1282)
Chromatin interactive
region (count:85)
LncRNA
region (count:34)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:3162 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:74489132-74489301	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:74343777-74343987	K562	blood:	n/a	n/a
3	ARID3A	chr16:74402200-74402343	K562	blood:	n/a	n/a
4	ARID3A	chr16:74343761-74344069	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:74494614-74494901	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:74340614-74340822	K562	blood:	n/a	n/a
7	ARID3A	chr16:74542563-74542915	K562	blood:	n/a	n/a
8	ARID3A	chr16:74581533-74581826	K562	blood:	n/a	n/a
9	ATF1	chr16:74402006-74402375	K562	blood:	n/a	chr16:74402193-74402207
10	ATF1	chr16:74568702-74568745	K562	blood:	n/a	n/a
11	ATF1	chr16:74542531-74542671	K562	blood:	n/a	n/a
12	ATF2	chr16:74486087-74486651	GM12878	blood:	n/a	n/a
13	ATF2	chr16:74527980-74528356	GM12878	blood:	n/a	n/a
14	ATF2	chr16:74464112-74464462	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr16:74401950-74402248	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
16	ATF3	chr16:74401896-74402310	K562	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
17	ATF3	chr16:74402079-74402253	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232
18	ATF3	chr16:74402012-74402314	H1-hESC	embryonic stem cell:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
19	ATF3	chr16:74401940-74402325	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
20	ATF3	chr16:74401853-74402428	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
21	BACH1	chr16:74402015-74402440	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr16:74542456-74542563	K562	blood:	n/a	n/a
23	BACH1	chr16:74398509-74398539	K562	blood:	n/a	n/a
24	BACH1	chr16:74356288-74356302	K562	blood:	n/a	n/a
25	BATF	chr16:74528004-74528257	GM12878	blood:	n/a	n/a
26	BATF	chr16:74363304-74363522	GM12878	blood:	n/a	n/a
27	BATF	chr16:74340348-74340594	GM12878	blood:	n/a	n/a
28	BATF	chr16:74463982-74464267	GM12878	blood:	n/a	n/a
29	BCL11A	chr16:74486263-74486524	GM12878	blood:	n/a	n/a
30	BCL11A	chr16:74527969-74528249	GM12878	blood:	n/a	chr16:74528169-74528178
31	BCL11A	chr16:74529322-74529490	GM12878	blood:	n/a	n/a
32	BCL3	chr16:74340156-74341682	A549	lung:	n/a	n/a
33	BCL3	chr16:74339512-74340098	A549	lung:	n/a	n/a
34	BCL3	chr16:74339747-74340167	K562	blood:	n/a	n/a
35	BCL3	chr16:74338505-74339423	A549	lung:	n/a	n/a
36	BCLAF1	chr16:74529244-74529549	GM12878	blood:	n/a	n/a
37	BCLAF1	chr16:74500738-74501138	GM12878	blood:	n/a	n/a
38	BHLHE40	chr16:74463983-74464410	GM12878	blood:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
39	BHLHE40	chr16:74363293-74363678	HepG2	liver:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
40	BHLHE40	chr16:74343713-74344036	HepG2	liver:	n/a	n/a
41	BHLHE40	chr16:74401879-74402451	HepG2	liver:	n/a	n/a
42	BHLHE40	chr16:74338044-74338054	HepG2	liver:	n/a	n/a
43	BHLHE40	chr16:74445450-74445698	HepG2	liver:	n/a	n/a
44	BHLHE40	chr16:74401987-74402336	A549	lung:	n/a	n/a
45	BHLHE40	chr16:74401340-74401505	GM12878	blood:	n/a	n/a
46	BHLHE40	chr16:74401339-74402424	K562	blood:	n/a	n/a
47	BHLHE40	chr16:74489396-74489957	HepG2	liver:	n/a	n/a
48	BHLHE40	chr16:74363303-74363604	GM12878	blood:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
49	BHLHE40	chr16:74464015-74464235	HepG2	liver:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
50	BHLHE40	chr16:74483125-74483307	K562	blood:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74456200-74456250	HCF	heart:	n/a
2	chr16:74456200-74456250	HCF	heart:	n/a
3	chr16:74446218-74446268	GM19239	blood:	n/a
4	chr16:74441639-74441689	NB4	blood:	n/a
5	chr16:74455140-74455190	ProgFib	skin:	n/a
6	chr16:74340046-74340096	RPTEC	kidney:	n/a
7	chr16:74455562-74455612	HL-60	blood:	n/a
8	chr16:74401794-74401844	HIPEpiC	eye:	n/a
9	chr16:74555139-74555189	SKMC	muscle:	n/a
10	chr16:74455448-74455498	AoSMC	blood vessel:	n/a
11	chr16:74446218-74446268	HUVEC	blood vessel:	n/a
12	chr16:74340046-74340096	GM12892	blood:	n/a
13	chr16:74441639-74441689	U87	brain:	n/a
14	chr16:74398168-74398218	PFSK-1	brain:	n/a
15	chr16:74455562-74455612	SK-N-SH	brain:	n/a
16	chr16:74403516-74403566	HEEpiC	esophagus:	n/a
17	chr16:74403516-74403566	Jurkat	blood:	n/a
18	chr16:74401794-74401844	GM19239	blood:	n/a
19	chr16:74455140-74455190	BJ	skin:	n/a
20	chr16:74441639-74441689	MCF10A-Er-Src	breast:	n/a
21	chr16:74555139-74555189	SK-N-SH	brain:	n/a
22	chr16:74455542-74455592	GM19239	blood:	n/a
23	chr16:74402336-74402386	GM12878	blood:	n/a
24	chr16:74402329-74402379	MCF-7	breast:	n/a
25	chr16:74455448-74455498	GM12878	blood:	n/a
26	chr16:74441639-74441689	HRPEpiC	eye:	n/a
27	chr16:74401794-74401844	HAEpiC	amniotic membrane:	n/a
28	chr16:74446218-74446268	SK-N-SH	brain:	n/a
29	chr16:74403516-74403566	HNPCEpiC	eye:	n/a
30	chr16:74441639-74441689	K562	blood:	n/a
31	chr16:74555139-74555189	T-47D	breast:	n/a
32	chr16:74555139-74555189	MCF-7	breast:	n/a
33	chr16:74446218-74446268	HNPCEpiC	eye:	n/a
34	chr16:74455542-74455592	CMK	blood:	n/a
35	chr16:74456200-74456250	ECC-1	luminal epithelium:	n/a
36	chr16:74403516-74403566	Hepatocyte	liver:	n/a
37	chr16:74555139-74555189	GM12892	blood:	n/a
38	chr16:74402329-74402379	HCPEpiC	choroid plexus:	n/a
39	chr16:74483694-74483744	HEEpiC	esophagus:	n/a
40	chr16:74402336-74402386	HCM	heart:	n/a
41	chr16:74441639-74441689	HEEpiC	esophagus:	n/a
42	chr16:74398168-74398218	Hepatocyte	liver:	n/a
43	chr16:74455448-74455498	Hela-S3	cervix:	n/a
44	chr16:74398168-74398218	GM12878	blood:	n/a
45	chr16:74456200-74456250	AG09319	gingival:	n/a
46	chr16:74446218-74446268	BE2_C	brain:	n/a
47	chr16:74401794-74401844	HCF	heart:	n/a
48	chr16:74402737-74402787	HRE	kidney:	n/a
49	chr16:74446218-74446268	NT2-D1	testis:	n/a
50	chr16:74403516-74403566	H1-hESC	embryonic stem cell:	embryo

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:74495671..74500050-chr16:74503781..74507841,5	MCF-7	breast:
2	chr16:74474948..74476830-chr16:74479473..74481845,2	MCF-7	breast:
3	chr16:74499520..74501485-chr16:74501761..74503824,2	MCF-7	breast:
4	chr16:74579440..74581506-chr16:74639502..74641032,2	MCF-7	breast:
5	chr16:74501191..74504078-chr16:74504630..74507267,3	K562	blood:
6	chr16:74481114..74483794-chr16:74490844..74493365,2	MCF-7	breast:
7	chr16:74497987..74500660-chr16:74639882..74642035,2	MCF-7	breast:
8	chr16:74536407..74538913-chr16:74540581..74542783,4	K562	blood:
9	chr16:74543683..74546204-chr16:74701058..74703476,2	K562	blood:
10	chr16:74338496..74341325-chr16:74351538..74353061,2	MCF-7	breast:
11	chr16:74541219..74543835-chr16:74544667..74546562,2	MCF-7	breast:
12	chr16:74534594..74537165-chr16:74541899..74543911,2	MCF-7	breast:
13	chr16:74463888..74464834-chr16:74487133..74487740,2	MCF-7	breast:
14	chr16:74515562..74517926-chr16:74520389..74521978,2	K562	blood:
15	chr16:74501191..74504078-chr16:74504630..74507267,3	K562	blood:
16	chr13:96705422..96706004-chr16:74337665..74338558,2	NB4	blood:
17	chr16:74467146..74469446-chr16:74472405..74475249,2	MCF-7	breast:
18	chr16:74514035..74516362-chr16:74518414..74521351,3	MCF-7	breast:
19	chr16:74276279..74277864-chr16:74338868..74341244,2	K562	blood:
20	chr16:74536407..74538913-chr16:74541075..74542783,2	K562	blood:
21	chr16:74534594..74537165-chr16:74541899..74543911,2	MCF-7	breast:
22	chr16:74504941..74507117-chr16:74507940..74509963,2	K562	blood:
23	chr16:74518172..74521190-chr16:74639634..74642594,6	MCF-7	breast:
24	chr16:74504176..74507094-chr16:74639050..74641052,2	MCF-7	breast:
25	chr16:74508736..74511342-chr16:74639774..74642134,3	MCF-7	breast:
26	chr16:74474948..74476830-chr16:74479473..74481845,2	MCF-7	breast:
27	chr16:74539035..74543243-chr16:74640061..74641958,3	MCF-7	breast:
28	chr16:74483167..74486389-chr16:74491599..74494939,3	MCF-7	breast:
29	chr16:74394116..74395645-chr3:9438342..9440027,2	MCF-7	breast:
30	chr16:74505094..74507584-chr16:74512027..74514149,2	MCF-7	breast:
31	chr16:74338414..74342140-chr16:74346350..74349350,4	K562	blood:
32	chr16:74520859..74523521-chr16:74528430..74530497,2	MCF-7	breast:
33	chr16:74484871..74487119-chr16:74488063..74490451,3	K562	blood:
34	chr16:74482713..74485167-chr16:74639325..74641867,3	MCF-7	breast:
35	chr16:74348919..74351200-chr16:74353361..74355371,2	K562	blood:
36	chr16:74343834..74344351-chr16:74486677..74487278,2	MCF-7	breast:
37	chr16:74333029..74335675-chr16:74353488..74356515,3	K562	blood:
38	chr16:74491887..74494202-chr16:74512320..74514365,2	MCF-7	breast:
39	chr16:74343323..74344029-chr16:74656867..74657812,2	MCF-7	breast:
40	chr16:74514035..74516362-chr16:74518414..74521351,3	MCF-7	breast:
41	chr16:74539026..74540750-chr16:74558493..74560677,2	MCF-7	breast:
42	chr16:74489287..74491803-chr16:74498510..74501318,2	K562	blood:
43	chr16:74536407..74538913-chr16:74540581..74542783,4	K562	blood:
44	chr16:74349759..74351336-chr16:74353263..74355191,2	MCF-7	breast:
45	chr16:74353334..74355532-chr16:74355748..74357983,4	K562	blood:
46	chr16:74349759..74351336-chr16:74353263..74355191,2	MCF-7	breast:
47	chr16:74470889..74473778-chr16:74634712..74637177,2	MCF-7	breast:
48	chr16:74540631..74542390-chr16:74543747..74546659,2	K562	blood:
49	chr16:74396107..74397775-chr16:74400703..74403254,2	K562	blood:
50	chr16:74519695..74521614-chr16:74523670..74527438,3	MCF-7	breast:

(count:34 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC18B-5	chr16:74351443-74352311	NONHSAT143674
2	lnc-NPIPL2-2	chr16:74468341-74468506	ENSG00000261170.1
3	lnc-CLEC18B-2	chr16:74343998-74344032	ENSG00000259972.1
4	lnc-NPIPL2-3	chr16:74496500-74496541	l_1361_chr16:74389381-74506276_brain
5	lnc-NPIPL2-2	chr16:74469068-74469152	ENSG00000261170.1
6	lnc-CLEC18B-5	chr16:74353763-74354252	NONHSAT143674
7	lnc-CLEC18B-2	chr16:74400933-74401582	NONHSAT143681
8	lnc-NPIPL2-4	chr16:74466397-74467374	NONHSAT143689
9	lnc-CLEC18B-5	chr16:74347924-74348600	NONHSAT143674
10	lnc-CLEC18B-5	chr16:74347204-74347745	NONHSAT143674
11	lnc-NPIPL2-2	chr16:74468703-74470867	NONHSAT143691
12	lnc-PSMD7-1	chr16:74349044-74349532	ENSG00000260884.1
13	lnc-PSMD7-2	chr16:74362373-74362939	NONHSAT143677
14	lnc-CLEC18B-5	chr16:74349041-74349919	NONHSAT143674
15	lnc-NPIPL2-5	chr16:74586149-74586644	NONHSAT143696
16	lnc-GLG1-1	chr16:74481325-74483790	ENSG00000260539.1
17	lnc-CLEC18B-2	chr16:74368790-74369244	ENSG00000259972.1
18	lnc-CLEC18B-2	chr16:74401963-74402046	NONHSAT143681
19	lnc-NPIPL2-2	chr16:74468341-74468597	ENSG00000261170.1
20	lnc-NPIPL2-3	chr16:74505853-74506276	l_1361_chr16:74389381-74506276_brain
21	lnc-CLEC18B-5	chr16:74346507-74346617	NONHSAT143673
22	lnc-CLEC18B-1	chr16:74411388-74411587	XLOC_012009
23	lnc-CLEC18B-5	chr16:74346927-74347288	NONHSAT143673
24	lnc-NPIPL2-3	chr16:74504826-74504910	l_1361_chr16:74389381-74506276_brain
25	lnc-NPIPL2-2	chr16:74467395-74468696	NONHSAT143690
26	lnc-CLEC18B-5	chr16:74349938-74350415	NONHSAT143674
27	lnc-NPIPL2-2	chr16:74456028-74456340	ENSG00000261170.1
28	lnc-PSMD7-1	chr16:74347235-74347258	ENSG00000260884.1
29	lnc-CLEC18B-5	chr16:74356132-74356732	NONHSAT143674
30	lnc-NPIPL2-3	chr16:74389382-74389428	l_1361_chr16:74389381-74506276_brain
31	lnc-NPIPL2-2	chr16:74456018-74456340	ENSG00000261170.1
32	lnc-NPIPL2-1	chr16:74401360-74403724	ENSG00000261079.1
33	lnc-CLEC18B-1	chr16:74411642-74411717	XLOC_012009
34	lnc-CLEC18B-5	chr16:74359871-74360683	NONHSAT143674

No data

(count:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PSMD7	hsa-miR-15b-5p	chr16:74339691-74339698
2	PSMD7	hsa-miR-15b-5p	chr16:74339679-74339698

Variant related genes	Relation type
ENSG00000239763	TF binding region
ENSG00000260539	TF binding region
RNU6-237P	TF binding region
ENSG00000261404	TF binding region
ENSG00000240861	TF binding region
NPIPB15	TF binding region
ENSG00000259972	TF binding region
ENSG00000261079	TF binding region
CLEC18B	TF binding region
PSMD7	TF binding region
ENSG00000260884	TF binding region
ENSG00000261170	TF binding region
GLG1	TF binding region
ENSG00000207525	TF binding region
ENSG00000214331	TF binding region
ENSG00000239763	CpG island
ENSG00000260539	CpG island
RNU6-237P	CpG island
ENSG00000261404	CpG island
ENSG00000240861	CpG island
NPIPB15	CpG island
ENSG00000259972	CpG island
ENSG00000261079	CpG island
CLEC18B	CpG island
PSMD7	CpG island
ENSG00000260884	CpG island
ENSG00000261170	CpG island
GLG1	CpG island
ENSG00000207525	CpG island
ENSG00000214331	CpG island
ENSG00000239763	chromatin interactions
ENSG00000261404	chromatin interactions
ENSG00000260884	chromatin interactions
ENSG00000102595	chromatin interactions
ENSG00000214331	chromatin interactions
ENSG00000259972	chromatin interactions
ENSG00000261079	chromatin interactions
ENSG00000090863	chromatin interactions
ENSG00000103035	chromatin interactions
ENSG00000207525	chromatin interactions
ENSG00000168411	chromatin interactions
ENSG00000168137	chromatin interactions
ENSG00000251794	chromatin interactions
ENSG00000206573	chromatin interactions
ENSG00000262904	chromatin interactions
ENSG00000260539	chromatin interactions

Extended variants
information (count: 11325 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:11325 , 50 per page) page: 1 2 3 4 5 6 7 ... 227

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527730798	chr16:74334781-74334782	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs547505348	chr16:74334821-74334822	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs570674709	chr16:74334822-74334823	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs189790319	chr16:74334870-74334871	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs550182085	chr16:74334887-74334888	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs570377167	chr16:74334888-74334889	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs373632849	chr16:74334895-74334896	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs369328599	chr16:74334916-74334917	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs576988646	chr16:74334922-74334923	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs563182701	chr16:74334929-74334930	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs537436459	chr16:74334976-74334977	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs575462071	chr16:74334981-74334982	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs150308557	chr16:74334999-74335000	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs138324633	chr16:74335038-74335039	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs376081054	chr16:74335060-74335061	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs548170879	chr16:74335076-74335077	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs141293105	chr16:74335105-74335106	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs74028226	chr16:74335108-74335109	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs17336700	chr16:74335204-74335205	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs576946766	chr16:74335239-74335240	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs180758078	chr16:74335249-74335250	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs376711005	chr16:74335257-74335258	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs145133598	chr16:74335266-74335267	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs576245144	chr16:74335377-74335378	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs79389551	chr16:74335384-74335385	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs561716957	chr16:74335386-74335387	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs36104509	chr16:74335392-74335393	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs373771092	chr16:74335436-74335437	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs200662962	chr16:74335498-74335499	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs200193234	chr16:74335499-74335500	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs556868796	chr16:74335510-74335511	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs186396573	chr16:74335562-74335563	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs541109889	chr16:74335635-74335636	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs138964596	chr16:74335657-74335658	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs140641866	chr16:74335683-74335684	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs550392526	chr16:74335694-74335695	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs143825830	chr16:74335763-74335764	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs561508499	chr16:74335764-74335765	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs148158962	chr16:74335772-74335773	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs373261200	chr16:74335774-74335775	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs190845927	chr16:74335823-74335824	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs568026439	chr16:74335843-74335844	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs533805888	chr16:74335871-74335872	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs113369108	chr16:74335880-74335881	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs368334716	chr16:74335881-74335882	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs76745772	chr16:74335904-74335905	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs570568007	chr16:74335907-74335908	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs539169226	chr16:74335908-74335909	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs112873799	chr16:74335957-74335958	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs548873092	chr16:74335981-74335982	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Epilepsy	20502679	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:5331 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:74331600-74334800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr16:74331800-74366400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:74332000-74342000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr16:74332200-74340600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr16:74332400-74335800	Weak transcription	Gastric	stomach
6	chr16:74332400-74337000	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr16:74332400-74340400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
8	chr16:74332400-74340600	Strong transcription	H1 Cell Line	embryonic stem cell
9	chr16:74332400-74340800	Strong transcription	H9 Cell Line	embryonic stem cell
10	chr16:74332400-74340800	Strong transcription	Osteobl	bone
11	chr16:74332400-74341200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr16:74332400-74341400	Strong transcription	NH-A	brain
13	chr16:74332400-74341600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr16:74332400-74341800	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr16:74332400-74342000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr16:74332400-74342400	Strong transcription	Fetal Thymus	thymus
17	chr16:74332400-74342600	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr16:74332600-74335000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr16:74332600-74335800	Weak transcription	Esophagus	oesophagus
20	chr16:74332600-74336600	Genic enhancers	HepG2	liver
21	chr16:74332600-74340600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
22	chr16:74332600-74341000	Strong transcription	HUES48 Cell Line	embryonic stem cell
23	chr16:74332600-74341400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr16:74332600-74341600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
25	chr16:74332600-74341600	Strong transcription	Brain Inferior Temporal Lobe	brain
26	chr16:74332600-74341600	Strong transcription	K562	blood
27	chr16:74332600-74342000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr16:74332600-74342000	Strong transcription	Primary B cells from peripheral blood	blood
29	chr16:74332600-74342000	Strong transcription	Primary hematopoietic stem cells	blood
30	chr16:74332600-74342000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr16:74332600-74342400	Strong transcription	Primary monocytes fromperipheralblood	blood
32	chr16:74332600-74342600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
33	chr16:74332600-74342600	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr16:74332600-74342800	Strong transcription	Brain Substantia Nigra	brain
35	chr16:74332800-74336000	Weak transcription	Right Atrium	heart
36	chr16:74332800-74338000	Strong transcription	Rectal Mucosa Donor 31	rectum
37	chr16:74332800-74340000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr16:74332800-74340000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr16:74332800-74340400	Strong transcription	Muscle Satellite Cultured Cells	--
40	chr16:74332800-74340600	Strong transcription	Brain Cingulate Gyrus	brain
41	chr16:74332800-74341600	Strong transcription	NHEK	skin
42	chr16:74332800-74342400	Strong transcription	Fetal Intestine Large	intestine
43	chr16:74332800-74342400	Strong transcription	Fetal Stomach	stomach
44	chr16:74332800-74342400	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr16:74332800-74342400	Strong transcription	Thymus	Thymus
46	chr16:74332800-74342600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr16:74332800-74342600	Strong transcription	Fetal Brain Female	brain
48	chr16:74332800-74342600	Strong transcription	Fetal Muscle Leg	muscle
49	chr16:74332800-74401200	Weak transcription	Stomach Mucosa	stomach
50	chr16:74333000-74341000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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