Variant report

Variant	nsv970172
Chromosome Location	chr6:150235248-150244455
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:304)
CpG islands
(count:794)
Chromatin interactive
region (count:13)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:150243580-150243643	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr6:150238023-150238354	K562	blood:	n/a	n/a
3	CBX3	chr6:150238111-150238594	K562	blood:	n/a	n/a
4	CEBPB	chr6:150244189-150244481	Hela-S3	cervix:	n/a	chr6:150244327-150244335
5	CEBPB	chr6:150244184-150244557	H1-hESC	embryonic stem cell:	n/a	chr6:150244327-150244335
6	CHD2	chr6:150243790-150244550	Hela-S3	cervix:	n/a	n/a
7	CTBP2	chr6:150243874-150244872	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr6:150237500-150237650	GM12869	blood:	n/a	n/a
9	CTCF	chr6:150238480-150238630	GM12873	blood:	n/a	n/a
10	CTCF	chr6:150238467-150238681	HepG2	liver:	n/a	n/a
11	CTCF	chr6:150238460-150238610	HAc	cerebellar:	n/a	n/a
12	CTCF	chr6:150238440-150238590	HFF-Myc	foreskin:	n/a	n/a
13	CTCF	chr6:150238384-150238748	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr6:150243760-150243910	NHDF-neo	bronchial:	n/a	n/a
15	CTCF	chr6:150238314-150238778	HCT-116	colon:	n/a	n/a
16	CTCF	chr6:150238312-150238688	A549	lung:	n/a	n/a
17	CTCF	chr6:150238508-150238610	LNCaP	prostate:	n/a	n/a
18	CTCF	chr6:150238420-150238570	GM12872	blood:	n/a	n/a
19	CTCF	chr6:150238500-150238650	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr6:150238440-150238590	HCM	heart:	n/a	n/a
21	CTCF	chr6:150238480-150238630	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr6:150238440-150238590	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr6:150243720-150243870	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr6:150238500-150238650	HEK293	kidney:	n/a	n/a
25	CTCF	chr6:150238160-150238310	HepG2	liver:	n/a	n/a
26	CTCF	chr6:150238460-150238610	BE2_C	brain:	n/a	n/a
27	CTCF	chr6:150238480-150238630	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr6:150243800-150243950	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr6:150238499-150238641	Fibrobl	skin:	n/a	n/a
30	CTCF	chr6:150238458-150238671	Gliobla	brain:	n/a	n/a
31	CTCF	chr6:150238376-150238743	K562	blood:	n/a	n/a
32	CTCF	chr6:150238480-150238630	AG10803	skin:	n/a	n/a
33	CTCF	chr6:150243835-150243840	IMR90	lung:	n/a	n/a
34	CTCF	chr6:150238440-150238590	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr6:150243860-150244010	HMEC	breast:	n/a	n/a
36	CTCF	chr6:150238140-150238390	HepG2	liver:	n/a	n/a
37	CTCF	chr6:150238460-150238610	HA-sp	spinal cord:	n/a	n/a
38	CTCF	chr6:150238520-150238670	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr6:150238480-150238630	HPF	lung:	n/a	n/a
40	CTCF	chr6:150238480-150238630	SAEC	small airway:	n/a	n/a
41	CTCF	chr6:150238460-150238610	A549	lung:	n/a	n/a
42	CTCF	chr6:150243700-150243990	AG04450	lung:	n/a	n/a
43	CTCF	chr6:150238460-150238610	WI-38	lung:	n/a	n/a
44	CTCF	chr6:150244353-150244361	K562	blood:	n/a	n/a
45	CTCF	chr6:150238456-150238665	HepG2	liver:	n/a	n/a
46	CTCF	chr6:150238514-150238629	GM19240	blood:	n/a	n/a
47	CTCF	chr6:150238536-150238599	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr6:150243760-150243910	AG09319	gingival:	n/a	n/a
49	CTCF	chr6:150243760-150243910	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr6:150238249-150238722	K562	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150238016-150238066	HCF	heart:	n/a
2	chr6:150238016-150238066	HCF	heart:	n/a
3	chr6:150242469-150242519	SKMC	muscle:	n/a
4	chr6:150244388-150244438	U87	brain:	n/a
5	chr6:150244392-150244442	GM12891	blood:	n/a
6	chr6:150242469-150242519	HCT-116	colon:	n/a
7	chr6:150242469-150242519	NHDF-neo	bronchial:	n/a
8	chr6:150244388-150244438	GM12878	blood:	n/a
9	chr6:150244204-150244254	SAEC	small airway:	n/a
10	chr6:150244204-150244254	NHBE	bronchial:	n/a
11	chr6:150244392-150244442	ProgFib	skin:	n/a
12	chr6:150238089-150238139	Hepatocyte	liver:	n/a
13	chr6:150238089-150238139	Caco-2	colon:	n/a
14	chr6:150244388-150244438	HCPEpiC	choroid plexus:	n/a
15	chr6:150240577-150240627	AG04449	skin:	fetal
16	chr6:150244204-150244254	HCF	heart:	n/a
17	chr6:150242469-150242519	GM12891	blood:	n/a
18	chr6:150244392-150244442	HRCEpiC	kidney:	n/a
19	chr6:150244392-150244442	GM06990	blood:	n/a
20	chr6:150238089-150238139	HRCEpiC	kidney:	n/a
21	chr6:150244288-150244338	HMEC	breast:	n/a
22	chr6:150244020-150244070	GM12892	blood:	n/a
23	chr6:150244204-150244254	A549	lung:	n/a
24	chr6:150238016-150238066	SK-N-SH	brain:	n/a
25	chr6:150242469-150242519	CMK	blood:	n/a
26	chr6:150238016-150238066	NH-A	brain:	n/a
27	chr6:150244388-150244438	SK-N-SH	brain:	n/a
28	chr6:150244020-150244070	NH-A	brain:	n/a
29	chr6:150238089-150238139	SK-N-MC	brain:	n/a
30	chr6:150240577-150240627	HL-60	blood:	n/a
31	chr6:150240577-150240627	HRPEpiC	eye:	n/a
32	chr6:150243903-150243953	AG04450	lung:	fetal
33	chr6:150238089-150238139	GM12878	blood:	n/a
34	chr6:150244323-150244373	HCT-116	colon:	n/a
35	chr6:150244020-150244070	CMK	blood:	n/a
36	chr6:150238016-150238066	CMK	blood:	n/a
37	chr6:150243903-150243953	NH-A	brain:	n/a
38	chr6:150238089-150238139	AG09319	gingival:	n/a
39	chr6:150243903-150243953	MCF-7	breast:	n/a
40	chr6:150238016-150238066	LNCaP	prostate:	n/a
41	chr6:150244295-150244345	HCF	heart:	n/a
42	chr6:150238016-150238066	Hepatocyte	liver:	n/a
43	chr6:150244388-150244438	CMK	blood:	n/a
44	chr6:150244388-150244438	GM12892	blood:	n/a
45	chr6:150244020-150244070	HRPEpiC	eye:	n/a
46	chr6:150238089-150238139	K562	blood:	n/a
47	chr6:150244295-150244345	Caco-2	colon:	n/a
48	chr6:150244020-150244070	HIPEpiC	eye:	n/a
49	chr6:150240577-150240627	HRE	kidney:	n/a
50	chr6:150244388-150244438	MCF10A-Er-Src	breast:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:149865589..149867401-chr6:150242514..150245357,2	MCF-7	breast:
2	chr6:150232168..150236512-chr6:150243000..150246593,4	K562	blood:
3	chr6:150237859..150240008-chr6:150242454..150244236,2	K562	blood:
4	chr6:150239646..150241708-chr6:150246246..150248253,2	K562	blood:
5	chr6:150186409..150189034-chr6:150239066..150241266,2	MCF-7	breast:
6	chr6:150181490..150187274-chr6:150243970..150248410,8	MCF-7	breast:
7	chr6:150182735..150186007-chr6:150239527..150243180,4	MCF-7	breast:
8	chr6:150215963..150217672-chr6:150235749..150238672,2	K562	blood:
9	chr6:150217021..150219534-chr6:150242538..150245487,2	MCF-7	breast:
10	chr6:150235746..150238768-chr6:150240556..150244338,4	MCF-7	breast:
11	chr6:150155391..150156182-chr6:150239663..150240372,2	MCF-7	breast:
12	chr6:150238077..150241849-chr6:150242731..150245993,5	MCF-7	breast:
13	chr6:150226570..150229723-chr6:150237444..150240125,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ULBP2-3	chr6:150240323-150240583	NONHSAT115517
2	lnc-ULBP2-3	chr6:150240323-150240644	ENSG00000223701.1
3	lnc-ULBP2-3	chr6:150240323-150240644	ENSG00000223701.3
4	lnc-ULBP2-3	chr6:150240323-150240642	ENSG00000223701.3

No data

Variant related genes	Relation type
RAET1G	TF binding region
RAET1G	CpG island
ENSG00000268592	chromatin interactions
ENSG00000203722	chromatin interactions
ENSG00000164520	chromatin interactions
ENSG00000131013	chromatin interactions
ENSG00000120256	chromatin interactions

Extended variants
information (count: 455 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:455 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371434297	chr6:150235256-150235257	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs58464560	chr6:150235261-150235262	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs150486653	chr6:150235338-150235339	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs187255372	chr6:150235370-150235371	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs9322231	chr6:150235394-150235395	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs145397510	chr6:150235456-150235457	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs369430318	chr6:150235468-150235469	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs149198457	chr6:150235494-150235495	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs554050818	chr6:150235495-150235496	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs573882137	chr6:150235511-150235512	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs139186033	chr6:150235551-150235552	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs375573420	chr6:150235564-150235565	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs141658533	chr6:150235588-150235589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs147050407	chr6:150235599-150235600	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544619590	chr6:150235613-150235614	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs573814314	chr6:150235634-150235635	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs578076783	chr6:150235654-150235655	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs71568294	chr6:150235708-150235709	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs77605952	chr6:150235765-150235766	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs560168519	chr6:150235767-150235768	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs191706876	chr6:150235853-150235854	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs141822480	chr6:150235884-150235885	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs536320185	chr6:150235910-150235911	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs6905778	chr6:150235933-150235934	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs150598114	chr6:150235967-150235968	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs571148612	chr6:150236003-150236004	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs138642270	chr6:150236023-150236024	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs547523952	chr6:150236067-150236068	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs546859186	chr6:150236073-150236074	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs113397788	chr6:150236102-150236103	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs556059990	chr6:150236111-150236112	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs4473864	chr6:150236123-150236124	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs538544614	chr6:150236209-150236210	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs57574929	chr6:150236214-150236215	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs10457854	chr6:150236215-150236216	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs35954356	chr6:150236237-150236238	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs535543528	chr6:150236239-150236240	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs184001869	chr6:150236248-150236249	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs141789835	chr6:150236275-150236276	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs146245632	chr6:150236295-150236296	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs4242281	chr6:150236308-150236309	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs188939202	chr6:150236331-150236332	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs192709013	chr6:150236348-150236349	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs532072768	chr6:150236369-150236370	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs183620380	chr6:150236371-150236372	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs62439751	chr6:150236427-150236428	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs10457855	chr6:150236429-150236430	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs374608958	chr6:150236446-150236447	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs113948606	chr6:150236461-150236462	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs200008606	chr6:150236471-150236472	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150226200-150242000	Weak transcription	Stomach Smooth Muscle	stomach
2	chr6:150227800-150243400	Weak transcription	Right Ventricle	heart
3	chr6:150230200-150239000	Weak transcription	Esophagus	oesophagus
4	chr6:150230400-150243600	Weak transcription	Pancreas	Pancrea
5	chr6:150231600-150239200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:150235000-150235400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr6:150235200-150235400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr6:150235200-150235400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr6:150235400-150238400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr6:150236600-150238800	Weak transcription	NHEK	skin
11	chr6:150237200-150243600	Weak transcription	Right Atrium	heart
12	chr6:150238400-150238600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr6:150238400-150239800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr6:150238800-150239400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr6:150238800-150239600	Enhancers	NHEK	skin
16	chr6:150239000-150239400	Enhancers	HMEC	breast
17	chr6:150239000-150239600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr6:150239000-150239800	Enhancers	Esophagus	oesophagus
19	chr6:150239200-150239400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr6:150239200-150239600	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr6:150239400-150239600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr6:150239400-150239800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:150239400-150240000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr6:150239400-150243200	Weak transcription	HMEC	breast
25	chr6:150239600-150243400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr6:150239600-150243400	Weak transcription	NHEK	skin
27	chr6:150239800-150243400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:150239800-150243400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr6:150239800-150243600	Weak transcription	Esophagus	oesophagus
30	chr6:150241200-150241400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr6:150241200-150243800	Weak transcription	Aorta	Aorta
32	chr6:150242400-150243800	Enhancers	Spleen	Spleen
33	chr6:150242600-150243000	Active TSS	Gastric	stomach
34	chr6:150242800-150247800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
35	chr6:150243000-150243400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr6:150243000-150243800	Bivalent Enhancer	Fetal Intestine Large	intestine
37	chr6:150243000-150243800	Weak transcription	Gastric	stomach
38	chr6:150243200-150243400	Enhancers	HMEC	breast
39	chr6:150243200-150243600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
40	chr6:150243400-150243600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
41	chr6:150243400-150243600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr6:150243400-150243600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr6:150243400-150243600	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr6:150243400-150243600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr6:150243400-150243600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
46	chr6:150243400-150243600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr6:150243400-150243600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr6:150243400-150243600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr6:150243400-150243600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr6:150243400-150243600	Active TSS	Brain Anterior Caudate	brain

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