Variant report

Variant	esv1801734
Chromosome Location	chr6:38986164-39034484
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:424)
CpG islands
(count:1038)
Chromatin interactive
region (count:37)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:39004705-39005449	K562	blood:	n/a	n/a
2	BACH1	chr6:38997248-38997532	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr6:39004752-39005119	K562	blood:	n/a	n/a
4	BHLHE40	chr6:39008820-39009201	GM12878	blood:	n/a	n/a
5	BRCA1	chr6:38997350-38997514	H1-hESC	embryonic stem cell:	n/a	n/a
6	CCNT2	chr6:39004558-39005133	K562	blood:	n/a	chr6:39004951-39004971
7	CCNT2	chr6:39016546-39016774	K562	blood:	n/a	n/a
8	CEBPB	chr6:38997444-38997571	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr6:38989658-38989814	K562	blood:	n/a	chr6:38989736-38989747 chr6:38989738-38989749 chr6:38989736-38989749
10	CEBPB	chr6:39004818-39005206	K562	blood:	n/a	chr6:39005009-39005020
11	CEBPB	chr6:38988768-38988964	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr6:38995870-38995998	HepG2	liver:	n/a	chr6:38995941-38995952
13	CEBPB	chr6:38995915-38996015	K562	blood:	n/a	chr6:38995941-38995952
14	CEBPB	chr6:39004799-39005176	K562	blood:	n/a	chr6:39005009-39005020
15	CEBPB	chr6:38989536-38989904	HepG2	liver:	n/a	chr6:38989540-38989553 chr6:38989736-38989747 chr6:38989738-38989749 chr6:38989736-38989749
16	CEBPD	chr6:39004723-39005265	K562	blood:	n/a	n/a
17	CEBPD	chr6:39004729-39005292	K562	blood:	n/a	n/a
18	CHD2	chr6:38997278-38997284	K562	blood:	n/a	n/a
19	CHD2	chr6:38997333-38997643	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr6:39008017-39008490	GM12878	blood:	n/a	n/a
21	CTBP2	chr6:39016260-39017332	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr6:38997320-38997470	HCM	heart:	n/a	n/a
23	CTCF	chr6:38997320-38997470	K562	blood:	n/a	n/a
24	CTCF	chr6:38997320-38997470	AG09309	skin:	n/a	n/a
25	CTCF	chr6:38997083-38997168	GM19240	blood:	n/a	n/a
26	CTCF	chr6:38997320-38997470	AG09319	gingival:	n/a	n/a
27	CTCF	chr6:38997244-38997560	Gliobla	brain:	n/a	n/a
28	CTCF	chr6:38997320-38997470	BJ	skin:	n/a	n/a
29	CTCF	chr6:38997199-38997606	K562	blood:	n/a	n/a
30	CTCF	chr6:38997183-38997589	K562	blood:	n/a	n/a
31	CTCF	chr6:38997300-38997450	GM12869	blood:	n/a	n/a
32	CTCF	chr6:38997340-38997490	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr6:38997300-38997450	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr6:38997320-38997470	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr6:39032080-39032230	Caco-2	colon:	n/a	n/a
36	CTCF	chr6:38997254-38997555	GM19239	blood:	n/a	n/a
37	CTCF	chr6:38997300-38997450	AG04449	skin:	n/a	n/a
38	CTCF	chr6:38997320-38997470	GM06990	blood:	n/a	n/a
39	CTCF	chr6:38997300-38997450	GM06990	blood:	n/a	n/a
40	CTCF	chr6:39032120-39032270	GM12873	blood:	n/a	n/a
41	CTCF	chr6:38997240-38997529	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr6:38997291-38997591	A549	lung:	n/a	n/a
43	CTCF	chr6:38997280-38997430	WI-38	lung:	n/a	n/a
44	CTCF	chr6:38997300-38997450	GM12872	blood:	n/a	n/a
45	CTCF	chr6:39017860-39018010	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr6:38997264-38997513	GM10248	blood:	n/a	n/a
47	CTCF	chr6:38997268-38997515	HepG2	liver:	n/a	n/a
48	CTCF	chr6:38996620-38996770	GM12865	blood:	n/a	n/a
49	CTCF	chr6:39032069-39032193	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:38997320-38997470	GM12875	blood:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:39022380-39022430	NH-A	brain:	n/a
2	chr6:39022380-39022430	NH-A	brain:	n/a
3	chr6:39016776-39016826	HIPEpiC	eye:	n/a
4	chr6:39016470-39016520	HEK293	kidney:	embryo
5	chr6:39022380-39022430	BJ	skin:	n/a
6	chr6:39016262-39016312	IMR90	lung:	fetal
7	chr6:39022380-39022430	AG09309	skin:	n/a
8	chr6:39016479-39016529	AG10803	skin:	n/a
9	chr6:39016479-39016529	PrEC	prostate:	n/a
10	chr6:38998315-38998365	HAEpiC	amniotic membrane:	n/a
11	chr6:39016470-39016520	CMK	blood:	n/a
12	chr6:39016326-39016376	PFSK-1	brain:	n/a
13	chr6:39020986-39021036	HCM	heart:	n/a
14	chr6:39013152-39013202	GM12891	blood:	n/a
15	chr6:39011018-39011068	HCM	heart:	n/a
16	chr6:39022380-39022430	HAEpiC	amniotic membrane:	n/a
17	chr6:38998315-38998365	HNPCEpiC	eye:	n/a
18	chr6:39011018-39011068	Caco-2	colon:	n/a
19	chr6:39022380-39022430	A549	lung:	n/a
20	chr6:39016326-39016376	NHBE	bronchial:	n/a
21	chr6:39016590-39016640	AG09319	gingival:	n/a
22	chr6:39016776-39016826	GM06990	blood:	n/a
23	chr6:38997395-38997445	ovcar-3	ovarian:	n/a
24	chr6:38998315-38998365	GM06990	blood:	n/a
25	chr6:39016326-39016376	GM12892	blood:	n/a
26	chr6:39016776-39016826	HRCEpiC	kidney:	n/a
27	chr6:39022380-39022430	AG04449	skin:	fetal
28	chr6:39016590-39016640	U87	brain:	n/a
29	chr6:39016776-39016826	A549	lung:	n/a
30	chr6:39011018-39011068	K562	blood:	n/a
31	chr6:38998315-38998365	U87	brain:	n/a
32	chr6:39015339-39015389	HCM	heart:	n/a
33	chr6:39016479-39016529	HL-60	blood:	n/a
34	chr6:39016363-39016413	Hepatocyte	liver:	n/a
35	chr6:39017116-39017166	Hela-S3	cervix:	n/a
36	chr6:39016262-39016312	Hela-S3	cervix:	n/a
37	chr6:39020986-39021036	MCF10A-Er-Src	breast:	n/a
38	chr6:39022380-39022430	HL-60	blood:	n/a
39	chr6:39017116-39017166	HUVEC	blood vessel:	n/a
40	chr6:39016326-39016376	HAEpiC	amniotic membrane:	n/a
41	chr6:39015339-39015389	AG04450	lung:	fetal
42	chr6:39011018-39011068	BE2_C	brain:	n/a
43	chr6:39016262-39016312	CMK	blood:	n/a
44	chr6:39016776-39016826	NHDF-neo	bronchial:	n/a
45	chr6:39016326-39016376	GM06990	blood:	n/a
46	chr6:39016590-39016640	HRCEpiC	kidney:	n/a
47	chr6:39015339-39015389	AG09309	skin:	n/a
48	chr6:38997395-38997445	AoSMC	blood vessel:	n/a
49	chr6:39016776-39016826	U87	brain:	n/a
50	chr6:39015339-39015389	PFSK-1	brain:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:39016643..39019473-chr6:39022041..39023583,2	K562	blood:
2	chr6:38998521..39000063-chr6:39004182..39006109,2	MCF-7	breast:
3	chr6:39008195..39010703-chr6:39012915..39015347,2	K562	blood:
4	chr6:38998129..39000751-chr6:39003691..39005962,2	K562	blood:
5	chr6:39025094..39027190-chr6:39031133..39033531,2	K562	blood:
6	chr6:38990306..38992412-chr6:38998180..39000571,2	K562	blood:
7	chr6:39006048..39008440-chr6:39019617..39021203,2	K562	blood:
8	chr6:38988197..38990916-chr6:39001925..39003826,3	MCF-7	breast:
9	chr6:38998129..39000751-chr6:39003691..39005962,2	K562	blood:
10	chr6:38984593..38986496-chr6:38994736..38997665,2	K562	blood:
11	chr6:38997318..38997990-chr6:39055855..39056407,2	MCF-7	breast:
12	chr6:39016886..39018824-chr6:39023068..39025617,2	MCF-7	breast:
13	chr6:39009574..39011759-chr6:39155267..39157602,2	K562	blood:
14	chr6:38998521..39000063-chr6:39004182..39006109,2	MCF-7	breast:
15	chr6:39006866..39009457-chr6:39013471..39015818,2	MCF-7	breast:
16	chr6:38997353..38997907-chr6:39070876..39071609,2	K562	blood:
17	chr6:39014216..39015762-chr6:39017423..39020213,2	K562	blood:
18	chr6:38990306..38992412-chr6:38998180..39000571,2	K562	blood:
19	chr6:38984593..38986496-chr6:38994736..38997665,2	K562	blood:
20	chr6:38997006..38997702-chr6:39125078..39125963,2	MCF-7	breast:
21	chr6:39032106..39033612-chr6:39039523..39041550,2	K562	blood:
22	chr6:39004865..39006783-chr6:39009275..39011836,2	K562	blood:
23	chr6:39016886..39018824-chr6:39023068..39025617,2	MCF-7	breast:
24	chr6:39004865..39006783-chr6:39009275..39011836,2	K562	blood:
25	chr4:134215031..134215860-chr6:38986253..38986839,2	K562	blood:
26	chr6:38988197..38990916-chr6:39001925..39003826,3	MCF-7	breast:
27	chr6:39014785..39017346-chr6:39021538..39023370,2	K562	blood:
28	chr6:39016643..39019473-chr6:39022041..39023583,2	K562	blood:
29	chr6:39014216..39015762-chr6:39017423..39020213,2	K562	blood:
30	chr6:39025094..39027190-chr6:39031133..39033531,2	K562	blood:
31	chr6:38997151..38998027-chr6:39059643..39060342,2	MCF-7	breast:
32	chr6:38984460..38985977-chr6:38987498..38989238,2	K562	blood:
33	chr6:38983654..38986496-chr6:38995790..38997665,2	K562	blood:
34	chr6:38976194..38979423-chr6:38983493..38987225,3	K562	blood:
35	chr6:38975629..38979423-chr6:38983493..38987291,5	K562	blood:
36	chr6:38983654..38986496-chr6:38995790..38997665,2	K562	blood:
37	chr6:39008195..39010703-chr6:39012915..39015347,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SAYSD1-2	chr6:39007379-39007761	NONHSAT112342

No data

Variant related genes	Relation type
ENSG00000220556	TF binding region
GLP1R	TF binding region
ENSG00000220556	CpG island
GLP1R	CpG island
ENSG00000220556	chromatin interactions
ENSG00000112164	chromatin interactions

Extended variants
information (count: 1912 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1912 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7766930	chr6:38986164-38986165	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149674411	chr6:38986244-38986245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145512522	chr6:38986247-38986248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540741888	chr6:38986248-38986249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529524778	chr6:38986256-38986257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549134860	chr6:38986275-38986276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148861652	chr6:38986276-38986277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531728067	chr6:38986319-38986320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs2281348	chr6:38986331-38986332	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs112856040	chr6:38986337-38986338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539686833	chr6:38986371-38986372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546803077	chr6:38986382-38986383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543438613	chr6:38986423-38986424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541539091	chr6:38986442-38986443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539323882	chr6:38986454-38986455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145346669	chr6:38986458-38986459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551195277	chr6:38986488-38986489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555086539	chr6:38986491-38986492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146597743	chr6:38986502-38986503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537548951	chr6:38986551-38986552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557882819	chr6:38986579-38986580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563614257	chr6:38986584-38986585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113864813	chr6:38986598-38986599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368387910	chr6:38986671-38986672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35532479	chr6:38986672-38986673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141357438	chr6:38986682-38986683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560289354	chr6:38986703-38986704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574013941	chr6:38986704-38986705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181667613	chr6:38986708-38986709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552426332	chr6:38986715-38986716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185723873	chr6:38986746-38986747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531683333	chr6:38986808-38986809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551480544	chr6:38986811-38986812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565414220	chr6:38986815-38986816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527765884	chr6:38986851-38986852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2281347	chr6:38986872-38986873	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs201786459	chr6:38986892-38986893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75658700	chr6:38986926-38986927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535396794	chr6:38986934-38986935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs145152917	chr6:38986953-38986954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs71571358	chr6:38986968-38986969	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs189014158	chr6:38987019-38987020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143694274	chr6:38987140-38987141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548354876	chr6:38987179-38987180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35144235	chr6:38987310-38987311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs28391256	chr6:38987321-38987322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62398586	chr6:38987352-38987353	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs577344428	chr6:38987355-38987356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533612536	chr6:38987372-38987373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115261791	chr6:38987382-38987383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	21693616	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Breast cancer	16397240	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Glioblastoma multiforme	21510904	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:492 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38985200-38986200	Weak transcription	Left Ventricle	heart
2	chr6:38985200-38986200	Weak transcription	Right Atrium	heart
3	chr6:38985400-38986600	Enhancers	Fetal Heart	heart
4	chr6:38985600-38986600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr6:38986000-38993600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr6:38986200-38986600	Enhancers	Left Ventricle	heart
7	chr6:38986200-38986600	Enhancers	Right Atrium	heart
8	chr6:38988800-38989400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr6:38988800-38989400	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr6:38988800-38989400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr6:38989000-38989200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
12	chr6:38989000-38989400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr6:38989200-38989800	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr6:38989400-38990200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr6:38989400-38994000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr6:38989400-38996600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr6:38989800-38996800	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr6:38990200-38990400	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr6:38990200-38990600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr6:38990400-38990600	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr6:38992000-38994200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr6:38992400-38999200	Weak transcription	Right Atrium	heart
23	chr6:38993600-38994200	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr6:38993800-38994400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:38994000-38994400	Enhancers	H9 Cell Line	embryonic stem cell
26	chr6:38994000-38994600	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr6:38994200-38994600	Enhancers	H1 Cell Line	embryonic stem cell
28	chr6:38994200-38994600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr6:38994200-38994600	Enhancers	Gastric	stomach
30	chr6:38994200-38999600	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr6:38994600-38996400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr6:38994600-38996600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr6:38995800-38996400	Enhancers	HMEC	breast
34	chr6:38996400-38996600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr6:38996600-38997000	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr6:38996800-38997000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr6:38996800-38997400	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr6:38999600-39000000	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr6:39003600-39003800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
40	chr6:39003600-39003800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr6:39003600-39003800	Enhancers	H9 Cell Line	embryonic stem cell
42	chr6:39003600-39003800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr6:39003600-39003800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr6:39003600-39006200	Enhancers	Fetal Heart	heart
45	chr6:39003800-39004800	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr6:39003800-39004800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr6:39004000-39005800	Enhancers	K562	blood
48	chr6:39004000-39006000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:39004200-39004400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
50	chr6:39004200-39005200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell

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