Variant report

Variant	nsv873883
Chromosome Location	chr2:38881106-38932777
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1148)
CpG islands
(count:733)
Chromatin interactive
region (count:91)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1148 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:38919989-38920328	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:38893914-38894509	K562	blood:	n/a	chr2:38894121-38894137
3	ARID3A	chr2:38892806-38893881	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:38881524-38881720	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:38917946-38918443	K562	blood:	n/a	n/a
6	ARID3A	chr2:38904891-38905252	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:38892880-38893239	K562	blood:	n/a	n/a
8	ARID3A	chr2:38912238-38912805	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:38928034-38928091	K562	blood:	n/a	n/a
10	ARID3A	chr2:38895975-38896159	K562	blood:	n/a	n/a
11	ARID3A	chr2:38917822-38918426	HepG2	liver:	n/a	n/a
12	ATF1	chr2:38932535-38932691	K562	blood:	n/a	n/a
13	ATF1	chr2:38918045-38918315	K562	blood:	n/a	n/a
14	ATF1	chr2:38881066-38882442	K562	blood:	n/a	n/a
15	ATF1	chr2:38929685-38929895	K562	blood:	n/a	n/a
16	ATF2	chr2:38890859-38891427	GM12878	blood:	n/a	n/a
17	ATF2	chr2:38921952-38922340	GM12878	blood:	n/a	n/a
18	ATF2	chr2:38880502-38881325	GM12878	blood:	n/a	n/a
19	ATF2	chr2:38892778-38893287	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr2:38893915-38894596	GM12878	blood:	n/a	n/a
21	ATF2	chr2:38892876-38893286	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr2:38893966-38894436	GM12878	blood:	n/a	n/a
23	ATF3	chr2:38917860-38918466	A549	lung:	n/a	n/a
24	ATF3	chr2:38892941-38893712	A549	lung:	n/a	n/a
25	ATF3	chr2:38917844-38918491	A549	lung:	n/a	n/a
26	ATF3	chr2:38917973-38918312	K562	blood:	n/a	n/a
27	ATF3	chr2:38912253-38912923	A549	lung:	n/a	n/a
28	BATF	chr2:38914812-38915129	GM12878	blood:	n/a	n/a
29	BATF	chr2:38921988-38922300	GM12878	blood:	n/a	n/a
30	BATF	chr2:38890987-38891390	GM12878	blood:	n/a	n/a
31	BATF	chr2:38924560-38924813	GM12878	blood:	n/a	n/a
32	BATF	chr2:38880553-38881370	GM12878	blood:	n/a	n/a
33	BCL11A	chr2:38890965-38891338	GM12878	blood:	n/a	n/a
34	BCL11A	chr2:38880543-38881471	GM12878	blood:	n/a	n/a
35	BCL3	chr2:38917811-38918387	A549	lung:	n/a	chr2:38918285-38918292
36	BCL3	chr2:38890959-38891353	GM12878	blood:	n/a	n/a
37	BCL3	chr2:38912275-38913346	A549	lung:	n/a	n/a
38	BCL3	chr2:38917723-38918506	A549	lung:	n/a	chr2:38918285-38918292
39	BCL3	chr2:38892736-38893577	A549	lung:	n/a	n/a
40	BCL3	chr2:38912120-38913350	A549	lung:	n/a	n/a
41	BCL3	chr2:38880884-38881268	GM12878	blood:	n/a	n/a
42	BCLAF1	chr2:38890948-38891335	GM12878	blood:	n/a	n/a
43	BCLAF1	chr2:38890899-38891425	GM12878	blood:	n/a	n/a
44	BCLAF1	chr2:38892808-38893415	GM12878	blood:	n/a	n/a
45	BCLAF1	chr2:38880691-38881233	GM12878	blood:	n/a	n/a
46	BHLHE40	chr2:38918059-38918297	K562	blood:	n/a	n/a
47	BHLHE40	chr2:38912924-38913154	A549	lung:	n/a	n/a
48	BHLHE40	chr2:38912530-38913203	HepG2	liver:	n/a	n/a
49	BHLHE40	chr2:38881205-38882055	HepG2	liver:	n/a	chr2:38881852-38881861
50	BHLHE40	chr2:38891043-38891243	GM12878	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:38894198-38894248	ovcar-3	ovarian:	n/a
2	chr2:38894198-38894248	ovcar-3	ovarian:	n/a
3	chr2:38892846-38892896	BE2_C	brain:	n/a
4	chr2:38893237-38893287	PFSK-1	brain:	n/a
5	chr2:38892846-38892896	MCF10A-Er-Src	breast:	n/a
6	chr2:38893251-38893301	LNCaP	prostate:	n/a
7	chr2:38893161-38893211	BE2_C	brain:	n/a
8	chr2:38892901-38892951	AG04450	lung:	fetal
9	chr2:38919351-38919401	Jurkat	blood:	n/a
10	chr2:38919351-38919401	U87	brain:	n/a
11	chr2:38893519-38893569	NB4	blood:	n/a
12	chr2:38892846-38892896	HEK293	kidney:	embryo
13	chr2:38894198-38894248	HRCEpiC	kidney:	n/a
14	chr2:38892309-38892359	NH-A	brain:	n/a
15	chr2:38892365-38892415	ProgFib	skin:	n/a
16	chr2:38892901-38892951	MCF-7	breast:	n/a
17	chr2:38892309-38892359	SK-N-MC	brain:	n/a
18	chr2:38892309-38892359	HCM	heart:	n/a
19	chr2:38893161-38893211	LNCaP	prostate:	n/a
20	chr2:38892901-38892951	U87	brain:	n/a
21	chr2:38893161-38893211	SK-N-SH_RA	brain:	n/a
22	chr2:38893237-38893287	SKMC	muscle:	n/a
23	chr2:38893251-38893301	GM12891	blood:	n/a
24	chr2:38894198-38894248	NHDF-neo	bronchial:	n/a
25	chr2:38894198-38894248	HMEC	breast:	n/a
26	chr2:38892365-38892415	GM12892	blood:	n/a
27	chr2:38894198-38894248	HIPEpiC	eye:	n/a
28	chr2:38894198-38894248	IMR90	lung:	fetal
29	chr2:38893519-38893569	SK-N-MC	brain:	n/a
30	chr2:38892958-38893008	Hela-S3	cervix:	n/a
31	chr2:38892846-38892896	HL-60	blood:	n/a
32	chr2:38892901-38892951	Jurkat	blood:	n/a
33	chr2:38893251-38893301	NHDF-neo	bronchial:	n/a
34	chr2:38919351-38919401	NHBE	bronchial:	n/a
35	chr2:38894198-38894248	HL-60	blood:	n/a
36	chr2:38893161-38893211	H1-hESC	embryonic stem cell:	embryo
37	chr2:38892958-38893008	Caco-2	colon:	n/a
38	chr2:38892887-38892937	GM12891	blood:	n/a
39	chr2:38894198-38894248	NB4	blood:	n/a
40	chr2:38893251-38893301	Caco-2	colon:	n/a
41	chr2:38892309-38892359	HMEC	breast:	n/a
42	chr2:38892846-38892896	IMR90	lung:	fetal
43	chr2:38892846-38892896	AG09319	gingival:	n/a
44	chr2:38892958-38893008	HCF	heart:	n/a
45	chr2:38919351-38919401	BE2_C	brain:	n/a
46	chr2:38893161-38893211	Jurkat	blood:	n/a
47	chr2:38892958-38893008	MCF-7	breast:	n/a
48	chr2:38892365-38892415	GM19239	blood:	n/a
49	chr2:38892901-38892951	RPTEC	kidney:	n/a
50	chr2:38893161-38893211	HIPEpiC	eye:	n/a

(count:91 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:38830892..38832834-chr2:38919143..38921497,2	K562	blood:
2	chr2:38838600..38841339-chr2:38925326..38927602,2	K562	blood:
3	chr2:38917783..38919456-chr2:38977277..38979712,2	MCF-7	breast:
4	chr2:38824210..38826669-chr2:38912161..38913673,2	MCF-7	breast:
5	chr2:38906476..38910309-chr2:38910692..38914128,4	K562	blood:
6	chr2:38881069..38883433-chr2:38890460..38892656,2	K562	blood:
7	chr2:38903554..38905525-chr2:38909598..38912564,2	MCF-7	breast:
8	chr2:38908524..38910141-chr2:38911332..38912843,2	MCF-7	breast:
9	chr2:38828746..38831144-chr2:38930016..38932480,2	MCF-7	breast:
10	chr2:38829496..38831232-chr2:38893143..38894875,2	MCF-7	breast:
11	chr2:38926804..38930306-chr2:38930620..38933051,3	K562	blood:
12	chr2:38920104..38923601-chr2:38924114..38926921,3	K562	blood:
13	chr2:38910654..38912179-chr2:38977560..38979833,2	K562	blood:
14	chr2:38879772..38882593-chr2:38978947..38981476,2	K562	blood:
15	chr2:38828302..38829916-chr2:38889127..38891080,2	K562	blood:
16	chr2:38818005..38820191-chr2:38893287..38895221,2	K562	blood:
17	chr2:38914950..38917916-chr2:38919871..38923223,3	K562	blood:
18	chr2:38867821..38870295-chr2:38895225..38897165,2	K562	blood:
19	chr2:38914282..38916559-chr2:38977085..38978615,2	MCF-7	breast:
20	chr2:38909532..38914838-chr2:38917160..38922190,4	K562	blood:
21	chr2:38819202..38822030-chr2:38909046..38911240,2	K562	blood:
22	chr2:38825670..38832919-chr2:38891527..38903424,21	K562	blood:
23	chr2:38827976..38829875-chr2:38912577..38914766,2	MCF-7	breast:
24	chr2:38908524..38910141-chr2:38911332..38912843,2	MCF-7	breast:
25	chr2:38823862..38826061-chr2:38919360..38922289,2	K562	blood:
26	chr2:38888499..38891196-chr2:38892046..38897483,5	K562	blood:
27	chr2:38885587..38887853-chr2:38899789..38902113,2	K562	blood:
28	chr2:38881069..38883433-chr2:38890460..38892656,2	K562	blood:
29	chr2:38893261..38895190-chr2:38902040..38904878,2	K562	blood:
30	chr2:38823156..38825243-chr2:38925773..38928004,2	K562	blood:
31	chr2:38823625..38826319-chr2:38903588..38906507,3	K562	blood:
32	chr2:38912803..38914727-chr2:38916699..38918326,2	MCF-7	breast:
33	chr2:38827534..38829774-chr2:38906960..38909388,3	K562	blood:
34	chr2:38827983..38829732-chr2:38929974..38932004,2	K562	blood:
35	chr2:38824811..38832919-chr2:38891494..38898299,16	K562	blood:
36	chr2:38884282..38886148-chr2:38894534..38896833,2	K562	blood:
37	chr2:38876173..38878521-chr2:38919650..38921533,2	MCF-7	breast:
38	chr2:38827954..38830677-chr2:38913858..38916720,4	K562	blood:
39	chr2:38827420..38830831-chr2:38879840..38883102,4	K562	blood:
40	chr2:38891861..38895889-chr2:38976029..38979857,7	K562	blood:
41	chr2:38827470..38830831-chr2:38880188..38882467,3	K562	blood:
42	chr2:38823851..38826080-chr2:38908814..38911340,2	K562	blood:
43	chr2:38917976..38920812-chr2:38977039..38979793,2	K562	blood:
44	chr2:38924892..38927572-chr2:38977178..38979733,2	MCF-7	breast:
45	chr2:38912803..38914727-chr2:38916699..38918326,2	MCF-7	breast:
46	chr2:38892930..38895051-chr2:38905642..38907216,2	K562	blood:
47	chr2:38897993..38900823-chr2:38904497..38907341,3	K562	blood:
48	chr2:38887947..38890064-chr2:38891296..38894559,3	K562	blood:
49	chr2:38920104..38923601-chr2:38924114..38926921,3	K562	blood:
50	chr2:38918111..38919788-chr2:38928353..38930489,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRPLL-2	chr2:38898496-38898563	ENSG00000232518.1
2	lnc-HNRPLL-2	chr2:38896001-38896210	ENSG00000232518.1
3	lnc-HNRPLL-2	chr2:38896481-38896680	ENSG00000232518.1
4	lnc-HNRPLL-2	chr2:38895830-38895903	ENSG00000232518.1

No data

Variant related genes	Relation type
GALM	TF binding region
ENSG00000232518	TF binding region
GALM	CpG island
ENSG00000232518	CpG island
ENSG00000136478	chromatin interactions
ENSG00000143889	chromatin interactions
ENSG00000232518	chromatin interactions
ENSG00000152147	chromatin interactions
ENSG00000235586	chromatin interactions
ENSG00000115875	chromatin interactions
ENSG00000143891	chromatin interactions

Extended variants
information (count: 2567 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2567 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6733848	chr2:38881106-38881107	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115366946	chr2:38881154-38881155	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs534345369	chr2:38881156-38881157	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs72913665	chr2:38881175-38881176	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs566826252	chr2:38881177-38881178	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs188148413	chr2:38881178-38881179	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs370402254	chr2:38881213-38881214	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs116004138	chr2:38881222-38881223	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs540823700	chr2:38881256-38881257	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs6704829	chr2:38881257-38881258	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs6748803	chr2:38881259-38881260	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs574810539	chr2:38881262-38881263	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs535721744	chr2:38881263-38881264	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs891705	chr2:38881272-38881273	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs72795169	chr2:38881341-38881342	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs184394218	chr2:38881346-38881347	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs565068467	chr2:38881364-38881365	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs148603609	chr2:38881457-38881458	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs112105648	chr2:38881477-38881478	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs190487657	chr2:38881478-38881479	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs891706	chr2:38881480-38881481	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs561696783	chr2:38881481-38881482	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs531733759	chr2:38881506-38881507	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs529225270	chr2:38881508-38881509	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs72795170	chr2:38881531-38881532	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs559678259	chr2:38881539-38881540	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs62142631	chr2:38881545-38881546	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs559768473	chr2:38881605-38881606	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs77221812	chr2:38881607-38881608	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs78937966	chr2:38881624-38881625	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs539126183	chr2:38881648-38881649	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs114735181	chr2:38881658-38881659	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs561268036	chr2:38881708-38881709	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs141378948	chr2:38881716-38881717	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs375155228	chr2:38881723-38881724	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs181909949	chr2:38881736-38881737	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs535752336	chr2:38881740-38881741	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs554081834	chr2:38881747-38881748	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs368410314	chr2:38881755-38881756	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs116611779	chr2:38881777-38881778	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs114274837	chr2:38881812-38881813	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs145234905	chr2:38881814-38881815	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs576103032	chr2:38881853-38881854	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs536475011	chr2:38881860-38881861	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs543123325	chr2:38881867-38881868	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs13393767	chr2:38881874-38881875	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs573923737	chr2:38881947-38881948	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs115606490	chr2:38881949-38881950	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs62142632	chr2:38881966-38881967	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs147987882	chr2:38881973-38881974	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1757 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:38870800-38881600	Weak transcription	Spleen	Spleen
2	chr2:38876000-38882000	Weak transcription	Thymus	Thymus
3	chr2:38877200-38882000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr2:38877200-38882200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr2:38878200-38888400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr2:38878400-38882000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr2:38878600-38883000	Enhancers	Primary T cells fromperipheralblood	blood
8	chr2:38878800-38881600	Enhancers	Stomach Mucosa	stomach
9	chr2:38879000-38881200	Enhancers	Duodenum Mucosa	Duodenum
10	chr2:38879000-38882000	Enhancers	Placenta	Placenta
11	chr2:38879000-38882800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr2:38879200-38882800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr2:38879400-38881400	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr2:38879400-38882200	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr2:38879400-38882200	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr2:38879400-38883000	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr2:38879400-38883000	Enhancers	Fetal Thymus	thymus
18	chr2:38879600-38881600	Enhancers	Hela-S3	cervix
19	chr2:38879600-38882000	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr2:38880000-38882600	Enhancers	Fetal Intestine Large	intestine
21	chr2:38880200-38881400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr2:38880200-38881800	Enhancers	Fetal Intestine Small	intestine
23	chr2:38880200-38881800	Enhancers	GM12878-XiMat	blood
24	chr2:38880200-38882400	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr2:38880400-38881200	Enhancers	Dnd41	blood
26	chr2:38880400-38882000	Enhancers	Primary hematopoietic stem cells	blood
27	chr2:38880600-38881200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr2:38880600-38882000	Flanking Active TSS	HepG2	liver
29	chr2:38880600-38882200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr2:38880800-38881200	Enhancers	HMEC	breast
31	chr2:38880800-38882000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr2:38880800-38882000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr2:38880800-38882200	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr2:38880800-38882400	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr2:38880800-38882400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr2:38881000-38881200	Enhancers	Small Intestine	intestine
37	chr2:38881000-38881400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr2:38881000-38881800	Flanking Active TSS	K562	blood
39	chr2:38881000-38882200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
40	chr2:38881000-38882400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr2:38881000-38882800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr2:38881400-38881600	Enhancers	Rectal Mucosa Donor 29	rectum
43	chr2:38881400-38881800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr2:38881400-38882000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr2:38881600-38881800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr2:38881600-38881800	Enhancers	Spleen	Spleen
47	chr2:38881800-38882200	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr2:38881800-38882800	Enhancers	K562	blood
49	chr2:38881800-38885800	Weak transcription	GM12878-XiMat	blood
50	chr2:38882000-38882400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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