Variant report

Variant	nsv969291
Chromosome Location	chr6:26274231-26276043
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:91)
CpG islands
(count:0)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:26273948-26274655	GM12878	blood:	n/a	n/a
2	ATF3	chr6:26273501-26274245	A549	lung:	n/a	n/a
3	BCLAF1	chr6:26273913-26274456	GM12878	blood:	n/a	n/a
4	BCLAF1	chr6:26272899-26274569	GM12878	blood:	n/a	n/a
5	CHD1	chr6:26269438-26274500	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD1	chr6:26270342-26274429	GM12878	blood:	n/a	n/a
7	FOXM1	chr6:26272807-26274345	GM12878	blood:	n/a	n/a
8	FOXM1	chr6:26273865-26274607	GM12878	blood:	n/a	n/a
9	GATA3	chr6:26274877-26275019	SH-SY5Y	brain:	n/a	n/a
10	GTF3C2	chr6:26273725-26274293	Hela-S3	cervix:	n/a	n/a
11	IRF1	chr6:26274225-26274359	K562	blood:	n/a	chr6:26274294-26274307 chr6:26274294-26274307 chr6:26274295-26274309 chr6:26274292-26274306 chr6:26274294-26274308 chr6:26274295-26274312 chr6:26274297-26274313 chr6:26274293-26274310 chr6:26274296-26274307 chr6:26274294-26274307 chr6:26274293-26274307
12	MTA3	chr6:26269886-26274743	GM12878	blood:	n/a	n/a
13	MXI1	chr6:26269688-26275175	SK-N-SH	brain:	n/a	n/a
14	NFATC1	chr6:26273895-26274535	GM12878	blood:	n/a	n/a
15	NFATC1	chr6:26272916-26274438	GM12878	blood:	n/a	n/a
16	NFIC	chr6:26270143-26274772	GM12878	blood:	n/a	chr6:26271787-26271815
17	NFYB	chr6:26274263-26274471	GM12878	blood:	n/a	n/a
18	PML	chr6:26272667-26274707	GM12878	blood:	n/a	n/a
19	POLR2A	chr6:26275671-26276782	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr6:26272814-26274590	HUVEC	blood vessel:	n/a	n/a
21	POLR2A	chr6:26272960-26274529	GM12891	blood:	n/a	n/a
22	POLR2A	chr6:26275946-26275953	MCF-7	breast:	n/a	n/a
23	POLR2A	chr6:26275995-26276013	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr6:26272872-26274688	GM12892	blood:	n/a	n/a
25	POLR2A	chr6:26272867-26274268	ProgFib	skin:	n/a	n/a
26	POLR2A	chr6:26272983-26274442	GM12892	blood:	n/a	n/a
27	POLR2A	chr6:26272888-26274370	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr6:26272950-26274626	GM12891	blood:	n/a	n/a
29	POLR2A	chr6:26272880-26274735	GM12878	blood:	n/a	n/a
30	POLR2A	chr6:26272087-26274531	HUVEC	blood vessel:	n/a	n/a
31	POLR2A	chr6:26275238-26275275	MCF-7	breast:	n/a	n/a
32	POLR2A	chr6:26272665-26274555	SK-N-SH	brain:	n/a	n/a
33	POLR2A	chr6:26269040-26274454	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr6:26272983-26274466	GM18505	blood:	n/a	n/a
35	POLR2A	chr6:26273966-26274349	H1-neurons	neurons:	n/a	n/a
36	POLR2A	chr6:26268330-26275103	MCF-7	breast:	n/a	n/a
37	POLR2A	chr6:26268317-26274794	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr6:26269675-26274774	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr6:26272911-26274601	GM12892	blood:	n/a	n/a
40	POLR2A	chr6:26272723-26274559	GM12891	blood:	n/a	n/a
41	POLR2A	chr6:26272937-26274449	GM12892	blood:	n/a	n/a
42	POLR2A	chr6:26272991-26274462	GM19099	blood:	n/a	n/a
43	POLR2A	chr6:26272943-26274805	GM12892	blood:	n/a	n/a
44	POLR2A	chr6:26274086-26274579	K562	blood:	n/a	n/a
45	POLR2A	chr6:26272431-26274472	GM18951	blood:	n/a	n/a
46	POLR2A	chr6:26273882-26274539	PANC-1	pancreas:	n/a	n/a
47	POLR2A	chr6:26273869-26274506	SK-N-SH	brain:	n/a	n/a
48	POLR2A	chr6:26266613-26275023	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr6:26275895-26275940	K562	blood:	n/a	n/a
50	POLR2A	chr6:26272963-26274319	U87	brain:	n/a	n/a

No data

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26270273..26274919-chr6:27857077..27861037,6	MCF-7	breast:
2	chr14:53257822..53258704-chr6:26273602..26274487,2	Hela-S3	cervix:
3	chr6:26270357..26275628-chr6:27773210..27778290,5	MCF-7	breast:
4	chr2:191744361..191746258-chr6:26273024..26275640,2	MCF-7	breast:
5	chr6:26216502..26217073-chr6:26273264..26274587,3	Hela-S3	cervix:
6	chr6:26271163..26276024-chr6:27111926..27116309,5	MCF-7	breast:
7	chr6:26272978..26274527-chr6:27776343..27778592,2	MCF-7	breast:
8	chr1:156252625..156254328-chr6:26272141..26274407,2	MCF-7	breast:
9	chr6:26273199..26275817-chr6:26322608..26324495,2	MCF-7	breast:
10	chr3:179958284..179960815-chr6:26273397..26275573,2	MCF-7	breast:
11	chr6:26020614..26023729-chr6:26272152..26276212,4	MCF-7	breast:
12	chr6:26024260..26027949-chr6:26272859..26275159,3	MCF-7	breast:
13	chr6:26270978..26274693-chr6:27098356..27103484,7	MCF-7	breast:
14	chr6:26033313..26036097-chr6:26273427..26274930,2	MCF-7	breast:
15	chr6:26271682..26274545-chr6:27832998..27834644,2	MCF-7	breast:
16	chr13:21258740..21261103-chr6:26273602..26276161,2	MCF-7	breast:
17	chr6:26273305..26276123-chr6:26535998..26538001,3	K562	blood:
18	chr14:50153414..50155005-chr6:26272692..26275211,2	MCF-7	breast:
19	chr16:89776016..89778632-chr6:26274025..26275904,2	MCF-7	breast:
20	chr13:36919647..36921156-chr6:26271932..26274514,2	MCF-7	breast:
21	chr6:26275391..26278113-chr6:27778905..27781292,2	MCF-7	breast:
22	chr6:26270164..26274435-chr6:27112425..27114820,4	MCF-7	breast:
23	chr6:26269718..26276565-chr6:27099393..27105112,10	MCF-7	breast:
24	chr6:26273638..26274247-chr9:114245827..114246827,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
HIST1H3G	TF binding region
HIST1H2APS4	TF binding region
ENSG00000265565	chromatin interactions
ENSG00000185130	chromatin interactions
ENSG00000187990	chromatin interactions
ENSG00000124635	chromatin interactions
ENSG00000115419	chromatin interactions
ENSG00000075399	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000124529	chromatin interactions
ENSG00000197903	chromatin interactions
ENSG00000198366	chromatin interactions
ENSG00000136813	chromatin interactions
ENSG00000184825	chromatin interactions
ENSG00000137259	chromatin interactions
ENSG00000203813	chromatin interactions
ENSG00000196176	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000196747	chromatin interactions
ENSG00000163472	chromatin interactions
ENSG00000100479	chromatin interactions
ENSG00000120664	chromatin interactions
ENSG00000261373	chromatin interactions
ENSG00000217862	chromatin interactions
ENSG00000100522	chromatin interactions
ENSG00000233224	chromatin interactions
ENSG00000133104	chromatin interactions
ENSG00000198374	chromatin interactions

Extended variants
information (count: 48 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:48 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111748162	chr6:26274237-26274238	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
2	rs145938997	chr6:26274252-26274253	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	27 gene(s)	Overlapped CNVs	n/a
3	rs183224909	chr6:26274298-26274299	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	27 gene(s)	Overlapped CNVs	n/a
4	rs16891516	chr6:26274310-26274311	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	27 gene(s)	Overlapped CNVs	n/a
5	rs74528506	chr6:26274314-26274315	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	27 gene(s)	Overlapped CNVs	n/a
6	rs186472262	chr6:26274355-26274356	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	27 gene(s)	Overlapped CNVs	n/a
7	rs139780981	chr6:26274361-26274362	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	27 gene(s)	Overlapped CNVs	n/a
8	rs77726908	chr6:26274391-26274392	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	27 gene(s)	Overlapped CNVs	n/a
9	rs6901096	chr6:26274418-26274419	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	26 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs552360379	chr6:26274436-26274437	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
11	rs146123585	chr6:26274479-26274480	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
12	rs6901243	chr6:26274498-26274499	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	25 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs548486577	chr6:26274544-26274545	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
14	rs61082103	chr6:26274566-26274567	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	22 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs560424961	chr6:26274575-26274576	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
16	rs533549618	chr6:26274635-26274636	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
17	rs35647639	chr6:26274980-26274981	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
18	rs78521733	chr6:26274982-26274983	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
19	rs570408790	chr6:26274995-26274996	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
20	rs192477039	chr6:26275009-26275010	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
21	rs140114588	chr6:26275012-26275013	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
22	rs576209855	chr6:26275068-26275069	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
23	rs542152995	chr6:26275070-26275071	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
24	rs142357757	chr6:26275106-26275107	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
25	rs183425165	chr6:26275110-26275111	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
26	rs572453214	chr6:26275116-26275117	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
27	rs375841451	chr6:26275175-26275176	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
28	rs539368331	chr6:26275196-26275197	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
29	rs541019923	chr6:26275285-26275286	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
30	rs80019342	chr6:26275400-26275401	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
31	rs188775683	chr6:26275465-26275466	Enhancers Weak transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
32	rs74638982	chr6:26275501-26275502	Enhancers Weak transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
33	rs562706003	chr6:26275557-26275558	Enhancers Weak transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
34	rs549652256	chr6:26275589-26275590	Enhancers Weak transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
35	rs531523806	chr6:26275623-26275624	Enhancers Weak transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
36	rs12665035	chr6:26275649-26275650	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs533737535	chr6:26275673-26275674	Enhancers Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs192657821	chr6:26275684-26275685	Enhancers Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs558830646	chr6:26275725-26275726	Enhancers Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs151282690	chr6:26275743-26275744	Enhancers Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs556970006	chr6:26275843-26275844	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs996020	chr6:26275876-26275877	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs567263027	chr6:26275877-26275878	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs539172958	chr6:26275916-26275917	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs182580136	chr6:26275947-26275948	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs140485676	chr6:26275977-26275978	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs73395313	chr6:26275985-26275986	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs544249355	chr6:26276018-26276019	Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Williams-beuren syndrome	16971481	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Autism	22495309	CNVD
Lung cancer	21569311	CNVD
Breast cancer	21509527	CNVD
Autism	20808228	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26269000-26274800	Active TSS	iPS-15b Cell Line	embryonic stem cell
2	chr6:26269200-26274600	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr6:26269200-26274600	Active TSS	iPS-18 Cell Line	embryonic stem cell
4	chr6:26269400-26274400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
5	chr6:26269400-26274400	Active TSS	HUES48 Cell Line	embryonic stem cell
6	chr6:26269400-26274800	Active TSS	H9 Cell Line	embryonic stem cell
7	chr6:26269400-26275000	Active TSS	H1 Cell Line	embryonic stem cell
8	chr6:26269800-26274400	Active TSS	HUES6 Cell Line	embryonic stem cell
9	chr6:26269800-26274400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:26269800-26274800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr6:26269800-26274800	Active TSS	NHLF	lung
12	chr6:26270000-26274600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:26270000-26274800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr6:26270200-26274400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr6:26270200-26274800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:26270400-26275400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr6:26270600-26274400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr6:26270600-26274600	Active TSS	Dnd41	blood
19	chr6:26270600-26274800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr6:26270600-26275000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr6:26270800-26274600	Active TSS	GM12878-XiMat	blood
22	chr6:26271200-26274400	Active TSS	Esophagus	oesophagus
23	chr6:26271200-26274400	Active TSS	Small Intestine	intestine
24	chr6:26271200-26274600	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
25	chr6:26271200-26274600	Bivalent/Poised TSS	Brain Substantia Nigra	brain
26	chr6:26271200-26274800	Active TSS	Right Ventricle	heart
27	chr6:26271200-26274800	Active TSS	HSMM	muscle
28	chr6:26271400-26274400	Bivalent/Poised TSS	Brain Angular Gyrus	brain
29	chr6:26271400-26274600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
30	chr6:26271400-26274800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr6:26271400-26274800	Active TSS	Aorta	Aorta
32	chr6:26271400-26274800	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
33	chr6:26271600-26274600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
34	chr6:26271600-26274800	Active TSS	Colonic Mucosa	Colon
35	chr6:26271600-26274800	Active TSS	Placenta Amnion	Placenta Amnion
36	chr6:26271600-26274800	Active TSS	Sigmoid Colon	Sigmoid Colon
37	chr6:26272000-26274600	Active TSS	Primary T killer memory cells from peripheral blood	blood
38	chr6:26272000-26274600	Active TSS	Duodenum Mucosa	Duodenum
39	chr6:26272000-26274600	Active TSS	Thymus	Thymus
40	chr6:26272000-26274800	Active TSS	HSMMtube	muscle
41	chr6:26272400-26274400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
42	chr6:26272400-26274400	Active TSS	Fetal Heart	heart
43	chr6:26272400-26274400	Active TSS	Fetal Kidney	kidney
44	chr6:26272400-26274600	Active TSS	Stomach Mucosa	stomach
45	chr6:26272400-26274800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr6:26272400-26274800	Active TSS	Fetal Intestine Small	intestine
47	chr6:26272400-26274800	Flanking Bivalent TSS/Enh	HepG2	liver
48	chr6:26272600-26274400	Active TSS	Primary T helper naive cells from peripheral blood	blood
49	chr6:26272600-26274400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
50	chr6:26272600-26274600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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