Variant report

Variant	nsv906911
Chromosome Location	chr16:75252526-75296247
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2583)
CpG islands
(count:2928)
Chromatin interactive
region (count:100)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2583 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:75284754-75284989	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:75285503-75285526	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:75267970-75268075	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:75278790-75279778	HepG2	liver:	n/a	n/a
5	ATF2	chr16:75252060-75252530	GM12878	blood:	n/a	n/a
6	ATF2	chr16:75267681-75268152	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr16:75287100-75287778	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr16:75267686-75268128	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr16:75278958-75279468	A549	lung:	n/a	chr16:75279119-75279128
10	BACH1	chr16:75290092-75290374	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr16:75287349-75287641	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr16:75284983-75285055	K562	blood:	n/a	n/a
13	BACH1	chr16:75267800-75268063	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr16:75252126-75252601	GM12878	blood:	n/a	chr16:75252274-75252284 chr16:75252239-75252247
15	BATF	chr16:75292159-75292381	GM12878	blood:	n/a	n/a
16	BATF	chr16:75272945-75273159	GM12878	blood:	n/a	chr16:75273058-75273068 chr16:75273062-75273072 chr16:75273057-75273068
17	BATF	chr16:75279083-75279318	GM12878	blood:	n/a	n/a
18	BCL11A	chr16:75252105-75252539	GM12878	blood:	n/a	chr16:75252272-75252281 chr16:75252235-75252244 chr16:75252273-75252282
19	BCL3	chr16:75278966-75279849	A549	lung:	n/a	chr16:75279177-75279190 chr16:75279200-75279209 chr16:75279429-75279438
20	BCL3	chr16:75278595-75279341	A549	lung:	n/a	chr16:75279177-75279190 chr16:75278842-75278851 chr16:75279200-75279209
21	BCL3	chr16:75285077-75285542	A549	lung:	n/a	chr16:75285477-75285490 chr16:75285464-75285477
22	BCL3	chr16:75274919-75275235	GM12878	blood:	n/a	n/a
23	BCL3	chr16:75287948-75288419	A549	lung:	n/a	n/a
24	BCL3	chr16:75261026-75261951	A549	lung:	n/a	n/a
25	BCL3	chr16:75258942-75259453	A549	lung:	n/a	n/a
26	BCL3	chr16:75279078-75279382	GM12878	blood:	n/a	chr16:75279177-75279190 chr16:75279200-75279209
27	BCL3	chr16:75260021-75261939	A549	lung:	n/a	n/a
28	BCL3	chr16:75260388-75260946	A549	lung:	n/a	n/a
29	BCL3	chr16:75267659-75268297	A549	lung:	n/a	n/a
30	BCL3	chr16:75259937-75260365	A549	lung:	n/a	n/a
31	BCLAF1	chr16:75267726-75268147	GM12878	blood:	n/a	n/a
32	BCLAF1	chr16:75267708-75268185	GM12878	blood:	n/a	n/a
33	BHLHE40	chr16:75267757-75268256	GM12878	blood:	n/a	chr16:75267840-75267856
34	BHLHE40	chr16:75256157-75256423	K562	blood:	n/a	n/a
35	BHLHE40	chr16:75285775-75285965	K562	blood:	n/a	n/a
36	BHLHE40	chr16:75267758-75268355	HepG2	liver:	n/a	chr16:75267840-75267856
37	BHLHE40	chr16:75267829-75268201	A549	lung:	n/a	chr16:75267840-75267856
38	BHLHE40	chr16:75284275-75285442	HepG2	liver:	n/a	chr16:75284384-75284400 chr16:75284817-75284833
39	BHLHE40	chr16:75284677-75284774	K562	blood:	n/a	n/a
40	BHLHE40	chr16:75267769-75268654	K562	blood:	n/a	chr16:75267840-75267856
41	BHLHE40	chr16:75278877-75279832	HepG2	liver:	n/a	n/a
42	BHLHE40	chr16:75279217-75279685	A549	lung:	n/a	n/a
43	BHLHE40	chr16:75290063-75290263	K562	blood:	n/a	n/a
44	BHLHE40	chr16:75296220-75296766	HepG2	liver:	n/a	n/a
45	BRCA1	chr16:75281445-75281519	HepG2	liver:	n/a	n/a
46	BRCA1	chr16:75296243-75296743	HepG2	liver:	n/a	n/a
47	BRCA1	chr16:75279192-75279828	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr16:75258440-75258489	HepG2	liver:	n/a	n/a
49	BRCA1	chr16:75278725-75279569	HepG2	liver:	n/a	n/a
50	BRCA1	chr16:75284521-75285348	HepG2	liver:	n/a	n/a

(count:2928 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:75263200-75263250	HRPEpiC	eye:	n/a
2	chr16:75286009-75286059	GM19239	blood:	n/a
3	chr16:75282051-75282101	GM19239	blood:	n/a
4	chr16:75283093-75283143	Jurkat	blood:	n/a
5	chr16:75287019-75287069	NB4	blood:	n/a
6	chr16:75289363-75289413	NB4	blood:	n/a
7	chr16:75252744-75252794	HRE	kidney:	n/a
8	chr16:75283093-75283143	HCPEpiC	choroid plexus:	n/a
9	chr16:75252973-75253023	Jurkat	blood:	n/a
10	chr16:75295370-75295420	NH-A	brain:	n/a
11	chr16:75286009-75286059	SK-N-MC	brain:	n/a
12	chr16:75271872-75271922	AoSMC	blood vessel:	n/a
13	chr16:75267857-75267907	HRCEpiC	kidney:	n/a
14	chr16:75285687-75285737	GM12891	blood:	n/a
15	chr16:75287019-75287069	BJ	skin:	n/a
16	chr16:75286915-75286965	SK-N-SH	brain:	n/a
17	chr16:75279566-75279616	MCF-7	breast:	n/a
18	chr16:75272306-75272356	SK-N-SH_RA	brain:	n/a
19	chr16:75264574-75264624	AG09309	skin:	n/a
20	chr16:75285526-75285576	SK-N-SH_RA	brain:	n/a
21	chr16:75263800-75263850	PANC-1	pancreas:	n/a
22	chr16:75282362-75282412	IMR90	lung:	fetal
23	chr16:75258780-75258830	Caco-2	colon:	n/a
24	chr16:75272306-75272356	AG09319	gingival:	n/a
25	chr16:75286009-75286059	HEK293	kidney:	embryo
26	chr16:75252619-75252669	GM19239	blood:	n/a
27	chr16:75285526-75285576	Hela-S3	cervix:	n/a
28	chr16:75269878-75269928	AG10803	skin:	n/a
29	chr16:75263551-75263601	HNPCEpiC	eye:	n/a
30	chr16:75263297-75263347	AG10803	skin:	n/a
31	chr16:75295370-75295420	SK-N-MC	brain:	n/a
32	chr16:75285726-75285776	HIPEpiC	eye:	n/a
33	chr16:75287019-75287069	HCF	heart:	n/a
34	chr16:75285489-75285539	AoSMC	blood vessel:	n/a
35	chr16:75285489-75285539	HAEpiC	amniotic membrane:	n/a
36	chr16:75266396-75266446	NHBE	bronchial:	n/a
37	chr16:75267857-75267907	HCT-116	colon:	n/a
38	chr16:75273344-75273394	GM19239	blood:	n/a
39	chr16:75285726-75285776	HL-60	blood:	n/a
40	chr16:75295370-75295420	GM12878	blood:	n/a
41	chr16:75272754-75272804	HIPEpiC	eye:	n/a
42	chr16:75269878-75269928	HMEC	breast:	n/a
43	chr16:75255590-75255640	HRPEpiC	eye:	n/a
44	chr16:75252973-75253023	GM12891	blood:	n/a
45	chr16:75285503-75285553	HNPCEpiC	eye:	n/a
46	chr16:75276399-75276449	AG10803	skin:	n/a
47	chr16:75276399-75276449	NT2-D1	testis:	n/a
48	chr16:75258780-75258830	HEEpiC	esophagus:	n/a
49	chr16:75285526-75285576	GM12892	blood:	n/a
50	chr16:75276399-75276449	HCPEpiC	choroid plexus:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:75267679..75270167-chr16:75298164..75300963,4	K562	blood:
2	chr16:75284019..75287279-chr16:75466611..75469457,3	MCF-7	breast:
3	chr16:75266558..75268435-chr16:75272216..75274328,2	K562	blood:
4	chr16:75239816..75243837-chr16:75256696..75260507,7	MCF-7	breast:
5	chr16:75260096..75262598-chr16:75274071..75277051,2	K562	blood:
6	chr16:75284175..75286207-chr16:75680901..75683623,2	MCF-7	breast:
7	chr16:75271315..75273372-chr16:75275391..75277280,2	K562	blood:
8	chr16:75285160..75285722-chr16:75299383..75300023,2	MCF-7	breast:
9	chr16:75182251..75184924-chr16:75259664..75261950,2	MCF-7	breast:
10	chr16:75288586..75292639-chr16:75337750..75340619,6	MCF-7	breast:
11	chr16:75291813..75293681-chr16:75338481..75340781,2	MCF-7	breast:
12	chr16:75265485..75267197-chr16:75295049..75296582,2	K562	blood:
13	chr16:75232930..75233869-chr16:75267627..75268399,2	MCF-7	breast:
14	chr16:75267828..75268434-chr16:75419147..75419726,2	MCF-7	breast:
15	chr16:75271644..75278130-chr16:75410170..75415316,7	MCF-7	breast:
16	chr16:75263332..75265712-chr16:75269441..75271613,2	K562	blood:
17	chr16:75265697..75267828-chr16:75295082..75297407,2	K562	blood:
18	chr16:75262796..75265611-chr16:75265904..75267442,2	MCF-7	breast:
19	chr16:75263871..75266298-chr16:75266366..75267894,2	K562	blood:
20	chr16:75263871..75266298-chr16:75266366..75267894,2	K562	blood:
21	chr16:75267476..75268387-chr16:75418859..75420095,9	MCF-7	breast:
22	chr16:75267887..75268393-chr16:75436507..75437336,2	K562	blood:
23	chr16:75281206..75283355-chr16:75320437..75323255,2	MCF-7	breast:
24	chr16:75267519..75268404-chr16:75418326..75418893,2	MCF-7	breast:
25	chr16:75282402..75286042-chr16:75337577..75341093,9	MCF-7	breast:
26	chr16:75288495..75290514-chr16:75396856..75398580,2	MCF-7	breast:
27	chr16:75244083..75246522-chr16:75263997..75266825,2	MCF-7	breast:
28	chr16:75290897..75293709-chr16:75420736..75422960,2	K562	blood:
29	chr16:75282975..75286210-chr16:75340217..75342691,3	K562	blood:
30	chr16:75259171..75262723-chr16:75263223..75268032,5	MCF-7	breast:
31	chr16:75258373..75260591-chr16:75260652..75263277,2	K562	blood:
32	chr16:75283944..75286001-chr16:75320233..75321893,2	MCF-7	breast:
33	chr16:75283733..75286666-chr17:57922628..57925329,2	MCF-7	breast:
34	chr16:75265697..75267828-chr16:75295082..75297407,2	K562	blood:
35	chr16:75268472..75270421-chr16:75272805..75274376,2	MCF-7	breast:
36	chr10:3214433..3215063-chr16:75285248..75285799,2	Hela-S3	cervix:
37	chr16:75257846..75260546-chr16:75267486..75270015,2	MCF-7	breast:
38	chr16:75261676..75264037-chr16:75269916..75271936,2	MCF-7	breast:
39	chr16:75295597..75297697-chr16:75338747..75341253,2	MCF-7	breast:
40	chr16:75278100..75280781-chr16:75467014..75469094,2	MCF-7	breast:
41	chr16:75267848..75268380-chr16:75436252..75437086,4	MCF-7	breast:
42	chr16:75265202..75266707-chr16:75338501..75340604,2	MCF-7	breast:
43	chr16:75281152..75283555-chr16:75283851..75285777,2	K562	blood:
44	chr16:75262796..75265611-chr16:75265904..75267442,2	MCF-7	breast:
45	chr16:75267412..75268233-chr16:75376465..75377161,3	MCF-7	breast:
46	chr16:75261304..75263525-chr16:75287372..75289617,2	K562	blood:
47	chr16:75271441..75274374-chr6:74228830..74231678,2	MCF-7	breast:
48	chr16:75239080..75244320-chr16:75282735..75286046,5	K562	blood:
49	chr16:75267386..75268402-chr16:75299374..75300473,4	MCF-7	breast:
50	chr1:117601739..117602655-chr16:75284708..75285399,2	NB4	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTRB1-1	chr16:75260545-75260623	NONHSAT143725
2	lnc-CTRB1-1	chr16:75259972-75260623	NONHSAT143724
3	lnc-CTRB1-1	chr16:75261888-75262093	NONHSAT143727
4	lnc-CTRB1-1	chr16:75261888-75262013	NONHSAT143725
5	lnc-CTRB1-1	chr16:75260239-75260290	NONHSAT143725
6	lnc-CTRB1-1	chr16:75260281-75260300	NR_109777
7	lnc-CTRB1-1	chr16:75260415-75260895	NONHSAT143726
8	lnc-CTRB1-1	chr16:75260989-75261204	NONHSAT143724
9	lnc-CTRB1-1	chr16:75261888-75262101	NR_109777
10	lnc-CTRB1-1	chr16:75260718-75260895	NONHSAT143724
11	lnc-CTRB1-2	chr16:75263574-75263637	l_1363_chr16:75170863-75242525_testes
12	lnc-CTRB1-1	chr16:75260989-75261204	NR_109777
13	lnc-CTRB1-1	chr16:75260718-75260895	NR_109777
14	lnc-CTRB1-1	chr16:75261888-75262093	NONHSAT143724
15	lnc-CTRB1-1	chr16:75261046-75261126	NONHSAT143725
16	lnc-CTRB1-1	chr16:75260884-75261204	NONHSAT143727
17	lnc-CTRB1-1	chr16:75260989-75261204	NONHSAT143726
18	lnc-CTRB1-1	chr16:75260391-75260623	NR_109777

No data

Variant related genes	Relation type
BCAR1	TF binding region
CTRB1	TF binding region
ENSG00000240338	TF binding region
BCAR1	CpG island
CTRB1	CpG island
ENSG00000240338	CpG island
ENSG00000168925	chromatin interactions
ENSG00000201524	chromatin interactions
ENSG00000168928	chromatin interactions
ENSG00000111011	chromatin interactions
ENSG00000240338	chromatin interactions
ENSG00000175387	chromatin interactions
ENSG00000245322	chromatin interactions
ENSG00000164032	chromatin interactions
ENSG00000184517	chromatin interactions
ENSG00000050820	chromatin interactions
ENSG00000074603	chromatin interactions
ENSG00000065427	chromatin interactions
ENSG00000252101	chromatin interactions
ENSG00000261783	chromatin interactions
ENSG00000259999	chromatin interactions
ENSG00000153774	chromatin interactions
ENSG00000236137	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000253154	chromatin interactions
ENSG00000166848	chromatin interactions
ENSG00000107959	chromatin interactions

Extended variants
information (count: 2457 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2457 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4243110	chr16:75252526-75252527	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547368614	chr16:75252536-75252537	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs113360345	chr16:75252549-75252550	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs141046805	chr16:75252562-75252563	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs562850339	chr16:75252573-75252574	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs531984556	chr16:75252585-75252586	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs191797758	chr16:75252587-75252588	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs562296949	chr16:75252599-75252600	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs149859828	chr16:75252611-75252612	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs546695209	chr16:75252620-75252621	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs566542635	chr16:75252683-75252684	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs145804612	chr16:75252688-75252689	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs567359564	chr16:75252696-75252697	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs552156644	chr16:75252702-75252703	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs148569966	chr16:75252711-75252712	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs538136523	chr16:75252717-75252718	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs372865018	chr16:75252733-75252734	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs554502497	chr16:75252738-75252739	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs112194127	chr16:75252744-75252745	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs533711438	chr16:75252775-75252776	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs553865593	chr16:75252797-75252798	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576884272	chr16:75252804-75252805	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs545794881	chr16:75252806-75252807	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs68181471	chr16:75252821-75252822	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs60727977	chr16:75252822-75252823	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs562897626	chr16:75252823-75252824	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs576704363	chr16:75252826-75252827	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs200976797	chr16:75252831-75252832	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs542490573	chr16:75252838-75252839	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs559791987	chr16:75252842-75252843	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs562169463	chr16:75252844-75252845	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs527905944	chr16:75252845-75252846	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs556189132	chr16:75252847-75252848	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs560822864	chr16:75252848-75252849	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs560294664	chr16:75252849-75252850	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs375578101	chr16:75252858-75252859	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532244143	chr16:75252867-75252868	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs200348377	chr16:75252869-75252870	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs375332929	chr16:75252878-75252879	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs199716713	chr16:75252901-75252902	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs112981559	chr16:75252902-75252903	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs1130448	chr16:75252941-75252942	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs1130449	chr16:75252942-75252943	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs1130450	chr16:75252947-75252948	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs1130452	chr16:75252948-75252949	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs1130453	chr16:75252951-75252952	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs1130454	chr16:75252956-75252957	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs201245474	chr16:75252957-75252958	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs371689386	chr16:75252967-75252968	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs375837360	chr16:75252994-75252995	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2412 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:75246800-75261000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr16:75249400-75254000	Enhancers	Placenta	Placenta
3	chr16:75250200-75254000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr16:75251400-75256200	Weak transcription	Right Atrium	heart
5	chr16:75251600-75261600	Weak transcription	HMEC	breast
6	chr16:75252200-75252600	Enhancers	Primary B cells from peripheral blood	blood
7	chr16:75252200-75252600	Enhancers	Brain Angular Gyrus	brain
8	chr16:75252200-75252600	Flanking Active TSS	GM12878-XiMat	blood
9	chr16:75252200-75253000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr16:75252200-75253200	Enhancers	Brain Anterior Caudate	brain
11	chr16:75252200-75253200	Enhancers	Brain Cingulate Gyrus	brain
12	chr16:75252200-75253400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
13	chr16:75252200-75253400	Enhancers	HSMM	muscle
14	chr16:75252200-75253600	Flanking Bivalent TSS/Enh	HepG2	liver
15	chr16:75252200-75254000	Enhancers	Brain Substantia Nigra	brain
16	chr16:75252200-75255000	Active TSS	Pancreas	Pancrea
17	chr16:75252400-75252600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr16:75252400-75252600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
19	chr16:75252400-75252600	Enhancers	Spleen	Spleen
20	chr16:75252400-75253200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr16:75252400-75253200	Enhancers	Fetal Muscle Leg	muscle
22	chr16:75252400-75253200	Enhancers	HSMMtube	muscle
23	chr16:75252400-75253400	Enhancers	Primary T helper naive cells from peripheral blood	blood
24	chr16:75252400-75253400	Enhancers	Dnd41	blood
25	chr16:75252400-75253800	Enhancers	Brain Hippocampus Middle	brain
26	chr16:75252600-75252800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr16:75252600-75253000	Enhancers	GM12878-XiMat	blood
28	chr16:75252600-75253400	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr16:75252600-75253600	Enhancers	Primary T cells fromperipheralblood	blood
30	chr16:75252600-75253600	Enhancers	Fetal Muscle Trunk	muscle
31	chr16:75252600-75254000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr16:75252600-75258200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr16:75252600-75262000	Weak transcription	Brain Angular Gyrus	brain
34	chr16:75252800-75253600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr16:75252800-75253600	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr16:75252800-75253600	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr16:75252800-75254600	Enhancers	Fetal Thymus	thymus
38	chr16:75253000-75253200	Enhancers	Primary T cells from cord blood	blood
39	chr16:75253000-75253200	Flanking Active TSS	GM12878-XiMat	blood
40	chr16:75253000-75253400	Enhancers	Thymus	Thymus
41	chr16:75253000-75253600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
42	chr16:75253000-75253600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr16:75253000-75253600	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr16:75253000-75253600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr16:75253000-75253600	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr16:75253000-75253800	Enhancers	Primary B cells from cord blood	blood
47	chr16:75253000-75254000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr16:75253000-75254600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
49	chr16:75253000-75256000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr16:75253200-75253600	Enhancers	GM12878-XiMat	blood

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