Variant report

Variant	esv2752390
Chromosome Location	chr10:27165095-27241780
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:27215887-27216043	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:27171003-27171296	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:27179954-27180055	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:27170979-27171143	K562	blood:	n/a	n/a
5	ATF1	chr10:27179886-27180171	K562	blood:	n/a	n/a
6	ATF2	chr10:27170788-27171173	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr10:27207852-27207903	K562	blood:	n/a	n/a
8	BACH1	chr10:27170965-27171226	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr10:27241137-27241377	GM12878	blood:	n/a	n/a
10	BATF	chr10:27241130-27241326	GM12878	blood:	n/a	n/a
11	BATF	chr10:27200819-27201093	GM12878	blood:	n/a	n/a
12	BATF	chr10:27239863-27240179	GM12878	blood:	n/a	n/a
13	BATF	chr10:27181459-27181814	GM12878	blood:	n/a	n/a
14	BATF	chr10:27239867-27240123	GM12878	blood:	n/a	n/a
15	BCL11A	chr10:27200762-27201086	GM12878	blood:	n/a	n/a
16	BCL11A	chr10:27181486-27181720	GM12878	blood:	n/a	n/a
17	BCL11A	chr10:27239855-27240184	GM12878	blood:	n/a	n/a
18	BCL11A	chr10:27181505-27181807	GM12878	blood:	n/a	n/a
19	BCL11A	chr10:27200770-27201068	GM12878	blood:	n/a	n/a
20	BCLAF1	chr10:27200661-27201146	GM12878	blood:	n/a	n/a
21	BCLAF1	chr10:27200699-27201097	GM12878	blood:	n/a	n/a
22	BCLAF1	chr10:27179830-27180212	GM12878	blood:	n/a	n/a
23	BCLAF1	chr10:27179765-27180187	GM12878	blood:	n/a	n/a
24	BHLHE40	chr10:27239962-27240121	GM12878	blood:	n/a	n/a
25	BHLHE40	chr10:27170980-27171190	GM12878	blood:	n/a	n/a
26	BHLHE40	chr10:27200766-27201161	GM12878	blood:	n/a	n/a
27	BHLHE40	chr10:27171034-27171240	K562	blood:	n/a	n/a
28	BHLHE40	chr10:27179920-27180158	HepG2	liver:	n/a	n/a
29	CBX3	chr10:27179886-27180178	K562	blood:	n/a	n/a
30	CCNT2	chr10:27220310-27220518	K562	blood:	n/a	n/a
31	CEBPB	chr10:27208365-27208582	HepG2	liver:	n/a	chr10:27208444-27208455
32	CEBPB	chr10:27171023-27171334	HepG2	liver:	n/a	n/a
33	CEBPB	chr10:27171013-27171310	A549	lung:	n/a	n/a
34	CEBPB	chr10:27215861-27216075	A549	lung:	n/a	n/a
35	CEBPB	chr10:27208377-27208567	H1-hESC	embryonic stem cell:	n/a	chr10:27208444-27208455
36	CEBPB	chr10:27170975-27171254	K562	blood:	n/a	n/a
37	CEBPB	chr10:27198634-27199009	K562	blood:	n/a	chr10:27198814-27198825 chr10:27198816-27198825 chr10:27198852-27198865 chr10:27198816-27198825 chr10:27198814-27198827 chr10:27198816-27198825 chr10:27198815-27198826 chr10:27198816-27198825 chr10:27198970-27198983
38	CEBPB	chr10:27171000-27171317	IMR90	lung:	n/a	n/a
39	CEBPB	chr10:27226988-27227113	A549	lung:	n/a	n/a
40	CEBPB	chr10:27215866-27216067	K562	blood:	n/a	n/a
41	CEBPB	chr10:27198729-27199004	H1-hESC	embryonic stem cell:	n/a	chr10:27198814-27198825 chr10:27198816-27198825 chr10:27198852-27198865 chr10:27198816-27198825 chr10:27198814-27198827 chr10:27198816-27198825 chr10:27198815-27198826 chr10:27198816-27198825 chr10:27198970-27198983
42	CEBPB	chr10:27171012-27171307	K562	blood:	n/a	n/a
43	CEBPB	chr10:27170981-27171302	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr10:27208346-27208628	A549	lung:	n/a	chr10:27208444-27208455
45	CEBPB	chr10:27208315-27208632	K562	blood:	n/a	chr10:27208444-27208455
46	CEBPB	chr10:27215887-27216002	IMR90	lung:	n/a	n/a
47	CEBPB	chr10:27198637-27199010	IMR90	lung:	n/a	chr10:27198814-27198825 chr10:27198816-27198825 chr10:27198852-27198865 chr10:27198816-27198825 chr10:27198814-27198827 chr10:27198816-27198825 chr10:27198815-27198826 chr10:27198816-27198825 chr10:27198970-27198983
48	CEBPB	chr10:27171018-27171316	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr10:27214768-27214801	HepG2	liver:	n/a	chr10:27214774-27214785
50	CEBPB	chr10:27198644-27199087	A549	lung:	n/a	chr10:27198814-27198825 chr10:27198816-27198825 chr10:27198852-27198865 chr10:27198816-27198825 chr10:27198814-27198827 chr10:27198816-27198825 chr10:27198815-27198826 chr10:27198816-27198825 chr10:27198970-27198983

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:27231882-27231932	MCF-7	breast:	n/a
2	chr10:27231882-27231932	MCF-7	breast:	n/a
3	chr10:27235627-27235677	AoSMC	blood vessel:	n/a
4	chr10:27220234-27220284	HNPCEpiC	eye:	n/a
5	chr10:27235598-27235648	HCM	heart:	n/a
6	chr10:27230955-27231005	AoSMC	blood vessel:	n/a
7	chr10:27231223-27231273	PANC-1	pancreas:	n/a
8	chr10:27232252-27232302	SKMC	muscle:	n/a
9	chr10:27230738-27230788	A549	lung:	n/a
10	chr10:27235514-27235564	SKMC	muscle:	n/a
11	chr10:27235514-27235564	NB4	blood:	n/a
12	chr10:27220441-27220491	SK-N-SH_RA	brain:	n/a
13	chr10:27231882-27231932	HIPEpiC	eye:	n/a
14	chr10:27231882-27231932	GM12892	blood:	n/a
15	chr10:27220234-27220284	GM12878	blood:	n/a
16	chr10:27231223-27231273	HCM	heart:	n/a
17	chr10:27230738-27230788	HCM	heart:	n/a
18	chr10:27231223-27231273	BJ	skin:	n/a
19	chr10:27231882-27231932	AG09309	skin:	n/a
20	chr10:27232252-27232302	NHDF-neo	bronchial:	n/a
21	chr10:27232252-27232302	NB4	blood:	n/a
22	chr10:27231882-27231932	ovcar-3	ovarian:	n/a
23	chr10:27232252-27232302	Hela-S3	cervix:	n/a
24	chr10:27194523-27194573	AG09309	skin:	n/a
25	chr10:27230738-27230788	ECC-1	luminal epithelium:	n/a
26	chr10:27194523-27194573	MCF-7	breast:	n/a
27	chr10:27220234-27220284	HPAEpiC	pulmonary alveolar:	n/a
28	chr10:27194523-27194573	GM19239	blood:	n/a
29	chr10:27232252-27232302	ProgFib	skin:	n/a
30	chr10:27194523-27194573	SK-N-SH	brain:	n/a
31	chr10:27232252-27232302	HRCEpiC	kidney:	n/a
32	chr10:27220441-27220491	AoSMC	blood vessel:	n/a
33	chr10:27231882-27231932	SKMC	muscle:	n/a
34	chr10:27230738-27230788	Jurkat	blood:	n/a
35	chr10:27220234-27220284	AG10803	skin:	n/a
36	chr10:27232252-27232302	BJ	skin:	n/a
37	chr10:27220441-27220491	HL-60	blood:	n/a
38	chr10:27194523-27194573	U87	brain:	n/a
39	chr10:27194523-27194573	HepG2	liver:	n/a
40	chr10:27235598-27235648	PrEC	prostate:	n/a
41	chr10:27230738-27230788	NHDF-neo	bronchial:	n/a
42	chr10:27232252-27232302	MCF-7	breast:	n/a
43	chr10:27194523-27194573	GM06990	blood:	n/a
44	chr10:27235627-27235677	HUVEC	blood vessel:	n/a
45	chr10:27235598-27235648	H1-hESC	embryonic stem cell:	embryo
46	chr10:27235627-27235677	HEEpiC	esophagus:	n/a
47	chr10:27220441-27220491	HRE	kidney:	n/a
48	chr10:27230955-27231005	GM12892	blood:	n/a
49	chr10:27232252-27232302	PFSK-1	brain:	n/a
50	chr10:27230955-27231005	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:27228167..27230462-chr10:27233630..27235621,2	MCF-7	breast:
2	chr10:27031601..27034238-chr10:27168698..27170803,2	MCF-7	breast:
3	chr10:26839774..26840368-chr10:27170775..27171534,2	MCF-7	breast:
4	chr10:27200392..27202294-chr10:27208159..27210444,2	MCF-7	breast:
5	chr10:27014809..27015628-chr10:27170414..27171655,4	MCF-7	breast:
6	chr10:26895059..26895568-chr10:27171114..27171693,2	K562	blood:
7	chr10:27147512..27150798-chr10:27165390..27168195,3	MCF-7	breast:
8	chr10:27159626..27161582-chr10:27169742..27171981,2	MCF-7	breast:
9	chr10:27174566..27175066-chr17:56736124..56737032,2	HCT-116	colon:
10	chr10:27014360..27015711-chr10:27170641..27171581,4	K562	blood:
11	chr10:27150071..27150642-chr10:27170538..27171586,3	MCF-7	breast:
12	chr10:26839671..26840332-chr10:27170680..27171574,2	K562	blood:
13	chr10:26984678..26987272-chr10:27166909..27168736,2	MCF-7	breast:
14	chr10:26988675..26990300-chr10:27168290..27169944,2	K562	blood:
15	chr10:27147900..27149546-chr10:27169189..27171150,2	MCF-7	breast:
16	chr10:27228167..27230462-chr10:27233630..27235621,2	MCF-7	breast:
17	chr10:27200392..27202294-chr10:27208159..27210444,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDSS1-2	chr10:27198340-27198867	XLOC_008422
2	lnc-PDSS1-2	chr10:27195824-27196025	XLOC_008422

Variant related genes	Relation type
LINC00202-1	TF binding region
LINC00614	TF binding region
LINC00202-1	CpG island
LINC00614	CpG island
ENSG00000148459	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000136754	chromatin interactions

Extended variants
information (count: 2923 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2923 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199985144	chr10:27165402-27165403	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs532831764	chr10:27165405-27165406	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs532704276	chr10:27165420-27165421	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs544609407	chr10:27165421-27165422	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs531039111	chr10:27165439-27165440	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs78131271	chr10:27165440-27165441	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs569234767	chr10:27165460-27165461	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs538167153	chr10:27165490-27165491	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs554705412	chr10:27165496-27165497	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs577989262	chr10:27165540-27165541	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs201693294	chr10:27165541-27165542	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs187409621	chr10:27165544-27165545	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554019478	chr10:27165549-27165550	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs550889634	chr10:27165563-27165564	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs189281410	chr10:27165568-27165569	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs546249576	chr10:27165569-27165570	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs113904287	chr10:27165578-27165579	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs556618375	chr10:27165585-27165586	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576371160	chr10:27165653-27165654	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs78426524	chr10:27165678-27165679	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs74743429	chr10:27165704-27165705	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs79666892	chr10:27165716-27165717	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs561821061	chr10:27165731-27165732	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs527542491	chr10:27165812-27165813	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541113348	chr10:27165829-27165830	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs72629742	chr10:27165863-27165864	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs578050313	chr10:27165873-27165874	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs34457713	chr10:27165913-27165914	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs146432138	chr10:27165968-27165969	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs549336551	chr10:27166043-27166044	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs75673661	chr10:27166094-27166095	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs7476015	chr10:27166108-27166109	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs531842496	chr10:27166112-27166113	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs548476144	chr10:27166154-27166155	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs568635237	chr10:27166189-27166190	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs540366365	chr10:27166232-27166233	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs534167603	chr10:27166241-27166242	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs368107906	chr10:27166259-27166260	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs554221598	chr10:27166286-27166287	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs570831308	chr10:27166310-27166311	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs12240787	chr10:27166316-27166317	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs556557156	chr10:27166320-27166321	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs147873268	chr10:27166324-27166325	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs542144567	chr10:27166327-27166328	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555418906	chr10:27166343-27166344	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs9664877	chr10:27166411-27166412	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs540894963	chr10:27166544-27166545	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs564326188	chr10:27166550-27166551	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs181646938	chr10:27166590-27166591	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs543119974	chr10:27166591-27166592	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	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 myeloid leukemia	20824076	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21525872	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27167600-27168400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr10:27167800-27169000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr10:27168200-27169400	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr10:27168600-27169000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr10:27168800-27169000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr10:27168800-27169000	Bivalent Enhancer	Fetal Lung	lung
7	chr10:27168800-27169000	Enhancers	A549	lung
8	chr10:27168800-27169000	Enhancers	NHEK	skin
9	chr10:27168800-27169200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr10:27169000-27170600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr10:27169000-27170600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr10:27169000-27170600	Weak transcription	NHEK	skin
13	chr10:27169200-27170400	Weak transcription	A549	lung
14	chr10:27170400-27170600	Enhancers	A549	lung
15	chr10:27170400-27170800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr10:27170600-27170800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr10:27170600-27170800	Enhancers	H9 Cell Line	embryonic stem cell
18	chr10:27170600-27170800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr10:27170600-27170800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr10:27170600-27170800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr10:27170600-27170800	Flanking Active TSS	Brain Anterior Caudate	brain
22	chr10:27170600-27170800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
23	chr10:27170600-27171000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr10:27170600-27171000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr10:27170600-27171000	Enhancers	Brain Cingulate Gyrus	brain
26	chr10:27170600-27171000	Enhancers	Brain Substantia Nigra	brain
27	chr10:27170600-27171000	Flanking Active TSS	A549	lung
28	chr10:27170600-27171000	Enhancers	NHEK	skin
29	chr10:27170600-27171400	Active TSS	ES-I3 Cell Line	embryonic stem cell
30	chr10:27170800-27171200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr10:27170800-27171200	Active TSS	Brain Anterior Caudate	brain
32	chr10:27170800-27171400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
33	chr10:27170800-27183200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr10:27171000-27171200	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr10:27171000-27171200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
36	chr10:27171000-27171400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr10:27171200-27172800	Weak transcription	A549	lung
38	chr10:27171400-27181600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr10:27173200-27173400	Enhancers	A549	lung
40	chr10:27176000-27176200	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
41	chr10:27176400-27176800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr10:27176400-27176800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr10:27176400-27177200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr10:27176400-27177200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr10:27176600-27176800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
46	chr10:27176600-27177000	Enhancers	Muscle Satellite Cultured Cells	--
47	chr10:27176600-27177200	Enhancers	NHEK	skin
48	chr10:27176600-27177400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr10:27179200-27180400	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr10:27179800-27180200	Enhancers	Fetal Brain Male	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links