Variant report

Variant	nsv551947
Chromosome Location	chr10:96154267-96162969
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:537)
CpG islands
(count:672)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:537 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:96161938-96162456	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:96158617-96158625	K562	blood:	n/a	n/a
3	ARID3A	chr10:96157433-96157887	HepG2	liver:	n/a	n/a
4	ATF1	chr10:96161937-96162267	K562	blood:	n/a	n/a
5	ATF2	chr10:96161841-96162276	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr10:96161816-96162293	A549	lung:	n/a	n/a
7	BACH1	chr10:96161959-96163255	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr10:96161704-96162598	A549	lung:	n/a	chr10:96162279-96162292 chr10:96162275-96162288 chr10:96162345-96162358
9	BCL3	chr10:96161717-96162346	A549	lung:	n/a	chr10:96162279-96162292 chr10:96162275-96162288
10	BCLAF1	chr10:96161767-96162712	GM12878	blood:	n/a	chr10:96162279-96162292 chr10:96162275-96162288 chr10:96162345-96162358
11	BCLAF1	chr10:96161801-96162945	GM12878	blood:	n/a	chr10:96162279-96162292 chr10:96162275-96162288 chr10:96162345-96162358
12	BHLHE40	chr10:96161860-96162771	K562	blood:	n/a	chr10:96162269-96162285
13	BHLHE40	chr10:96161931-96162433	HepG2	liver:	n/a	chr10:96162269-96162285
14	BHLHE40	chr10:96161878-96163759	GM12878	blood:	n/a	chr10:96162269-96162285
15	BRCA1	chr10:96161930-96162118	GM12878	blood:	n/a	n/a
16	BRCA1	chr10:96157461-96157798	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr10:96161648-96162699	HCT-116	colon:	n/a	n/a
18	CBX3	chr10:96161727-96162379	K562	blood:	n/a	n/a
19	CBX3	chr10:96161771-96162241	K562	blood:	n/a	n/a
20	CCNT2	chr10:96162008-96163594	K562	blood:	n/a	n/a
21	CEBPB	chr10:96161853-96162658	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr10:96161752-96162087	HepG2	liver:	n/a	n/a
23	CEBPB	chr10:96161693-96162588	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPD	chr10:96162024-96162440	HepG2	liver:	n/a	n/a
25	CHD1	chr10:96162753-96162837	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr10:96162127-96163963	GM12878	blood:	n/a	n/a
27	CHD2	chr10:96162586-96162957	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr10:96161910-96162820	GM12878	blood:	n/a	n/a
29	CHD2	chr10:96162018-96162281	HepG2	liver:	n/a	n/a
30	CHD2	chr10:96162486-96162758	HepG2	liver:	n/a	n/a
31	CHD2	chr10:96161949-96162261	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr10:96162751-96162799	K562	blood:	n/a	n/a
33	CHD2	chr10:96161884-96163836	Hela-S3	cervix:	n/a	n/a
34	CREB1	chr10:96161849-96162867	A549	lung:	n/a	n/a
35	CREB1	chr10:96161777-96163798	HepG2	liver:	n/a	n/a
36	CREB1	chr10:96161921-96163009	GM12878	blood:	n/a	n/a
37	CREB1	chr10:96161983-96162256	A549	lung:	n/a	n/a
38	CREB1	chr10:96161934-96162453	ECC-1	luminal epithelium:	n/a	n/a
39	CTBP2	chr10:96162076-96163543	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr10:96161940-96162568	GM12878	blood:	n/a	n/a
41	CTCF	chr10:96162320-96162470	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr10:96162660-96162810	GM12871	blood:	n/a	n/a
43	CTCF	chr10:96162482-96162573	Fibrobl	skin:	n/a	n/a
44	CTCF	chr10:96161920-96162070	AG09319	gingival:	n/a	n/a
45	CTCF	chr10:96162445-96162527	GM12891	blood:	n/a	n/a
46	CTCF	chr10:96162480-96162630	GM12864	blood:	n/a	n/a
47	CTCF	chr10:96162085-96162159	Lung_OC	lung:	n/a	n/a
48	CTCF	chr10:96162492-96162574	NHEK	skin:	n/a	n/a
49	CTCF	chr10:96162080-96162230	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr10:96162420-96162570	SAEC	small airway:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:96162066-96162116	AG09319	gingival:	n/a
2	chr10:96162066-96162116	AG09319	gingival:	n/a
3	chr10:96162178-96162228	SK-N-SH_RA	brain:	n/a
4	chr10:96161889-96161939	U87	brain:	n/a
5	chr10:96162066-96162116	Hepatocyte	liver:	n/a
6	chr10:96162189-96162239	HCF	heart:	n/a
7	chr10:96162066-96162116	Caco-2	colon:	n/a
8	chr10:96162178-96162228	NB4	blood:	n/a
9	chr10:96162173-96162223	SK-N-SH	brain:	n/a
10	chr10:96162066-96162116	CMK	blood:	n/a
11	chr10:96162178-96162228	GM12891	blood:	n/a
12	chr10:96162133-96162183	MCF-7	breast:	n/a
13	chr10:96162809-96162859	CMK	blood:	n/a
14	chr10:96162284-96162334	HepG2	liver:	n/a
15	chr10:96161916-96161966	BJ	skin:	n/a
16	chr10:96162133-96162183	NHDF-neo	bronchial:	n/a
17	chr10:96162178-96162228	HRPEpiC	eye:	n/a
18	chr10:96162146-96162196	AG10803	skin:	n/a
19	chr10:96162066-96162116	NH-A	brain:	n/a
20	chr10:96162066-96162116	K562	blood:	n/a
21	chr10:96162173-96162223	Jurkat	blood:	n/a
22	chr10:96161916-96161966	GM19239	blood:	n/a
23	chr10:96162173-96162223	AoSMC	blood vessel:	n/a
24	chr10:96162133-96162183	AG09319	gingival:	n/a
25	chr10:96162173-96162223	SK-N-SH_RA	brain:	n/a
26	chr10:96162146-96162196	SK-N-SH	brain:	n/a
27	chr10:96162173-96162223	LNCaP	prostate:	n/a
28	chr10:96162133-96162183	BE2_C	brain:	n/a
29	chr10:96162162-96162212	SAEC	small airway:	n/a
30	chr10:96162146-96162196	HPAEpiC	pulmonary alveolar:	n/a
31	chr10:96162162-96162212	SK-N-SH_RA	brain:	n/a
32	chr10:96162066-96162116	AoSMC	blood vessel:	n/a
33	chr10:96162284-96162334	Hela-S3	cervix:	n/a
34	chr10:96162146-96162196	HRCEpiC	kidney:	n/a
35	chr10:96161889-96161939	HEK293	kidney:	embryo
36	chr10:96162066-96162116	ovcar-3	ovarian:	n/a
37	chr10:96162146-96162196	SK-N-SH_RA	brain:	n/a
38	chr10:96161889-96161939	HIPEpiC	eye:	n/a
39	chr10:96162189-96162239	HAEpiC	amniotic membrane:	n/a
40	chr10:96162066-96162116	HRCEpiC	kidney:	n/a
41	chr10:96162189-96162239	MCF10A-Er-Src	breast:	n/a
42	chr10:96162284-96162334	SK-N-MC	brain:	n/a
43	chr10:96161889-96161939	ProgFib	skin:	n/a
44	chr10:96162066-96162116	HRPEpiC	eye:	n/a
45	chr10:96162066-96162116	NB4	blood:	n/a
46	chr10:96162133-96162183	HCT-116	colon:	n/a
47	chr10:96162178-96162228	A549	lung:	n/a
48	chr10:96162066-96162116	HAEpiC	amniotic membrane:	n/a
49	chr10:96162066-96162116	HCM	heart:	n/a
50	chr10:96161916-96161966	AG04450	lung:	fetal

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:96162530..96165019-chr10:96199067..96201077,2	MCF-7	breast:
2	chr10:96161889..96162635-chr9:88897007..88897760,2	Hela-S3	cervix:
3	chr10:96120934..96124258-chr10:96160439..96165957,6	MCF-7	breast:
4	chr10:96162017..96163519-chr15:65596803..65598979,2	MCF-7	breast:
5	chr10:96157876..96161073-chr10:96161693..96163507,3	MCF-7	breast:
6	chr10:96162673..96164608-chr10:96201520..96204137,3	MCF-7	breast:
7	chr10:96121730..96122942-chr10:96161863..96162614,3	Hela-S3	cervix:
8	chr10:96154206..96156824-chr10:96158509..96161283,2	MCF-7	breast:
9	chr10:96122264..96123877-chr10:96154739..96156763,2	MCF-7	breast:
10	chr10:96154206..96156824-chr10:96158509..96161283,2	MCF-7	breast:
11	chr10:96162267..96164235-chr10:96185502..96188240,3	MCF-7	breast:
12	chr10:96162121..96162677-chr5:154317419..154318125,2	HCT-116	colon:
13	chr10:96162891..96164490-chr10:96175616..96177129,2	MCF-7	breast:
14	chr10:96121306..96124383-chr10:96159927..96163798,5	MCF-7	breast:
15	chr10:96162368..96164918-chr10:96174079..96176855,3	K562	blood:
16	chr10:96162320..96165263-chr10:96165537..96170524,5	K562	blood:
17	chr10:96159758..96162488-chr10:96305268..96307065,2	K562	blood:
18	chr10:96151144..96155303-chr10:96160392..96163216,4	K562	blood:
19	chr10:96121005..96123981-chr10:96160609..96162843,2	K562	blood:
20	chr10:96122660..96124273-chr10:96159058..96162494,4	K562	blood:
21	chr10:96160448..96164371-chr10:96304138..96307716,8	MCF-7	breast:
22	chr10:96153074..96157080-chr10:96161760..96164291,4	MCF-7	breast:

No data

Variant related genes	Relation type
TBC1D12	TF binding region
TBC1D12	CpG island
ENSG00000119969	chromatin interactions
ENSG00000135070	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000173145	chromatin interactions
ENSG00000082516	chromatin interactions
ENSG00000108239	chromatin interactions

Extended variants
information (count: 341 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:341 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12260755	chr10:96154267-96154268	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs376206582	chr10:96154283-96154284	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs548247121	chr10:96154345-96154346	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs79370509	chr10:96154425-96154426	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs568565138	chr10:96154498-96154499	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs568227497	chr10:96154553-96154554	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs144986044	chr10:96154604-96154605	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs149086225	chr10:96154612-96154613	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs189652689	chr10:96154703-96154704	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs547455280	chr10:96154705-96154706	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs539719066	chr10:96154712-96154713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs566205044	chr10:96154713-96154714	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs573318965	chr10:96154804-96154805	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs143162623	chr10:96154825-96154826	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs555196698	chr10:96154833-96154834	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs80259668	chr10:96154834-96154835	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs543818091	chr10:96154845-96154846	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs193059076	chr10:96154851-96154852	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs185292076	chr10:96154893-96154894	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs540115011	chr10:96154894-96154895	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs564653325	chr10:96154904-96154905	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs35018496	chr10:96154905-96154906	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs397741177	chr10:96154918-96154919	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs140232243	chr10:96154963-96154964	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs530400814	chr10:96154976-96154977	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs539737380	chr10:96155004-96155005	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529124373	chr10:96155030-96155031	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs549139530	chr10:96155064-96155065	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs536966878	chr10:96155110-96155111	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs562199649	chr10:96155121-96155122	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs530993349	chr10:96155145-96155146	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs113005088	chr10:96155159-96155160	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs556827835	chr10:96155177-96155178	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs570814580	chr10:96155190-96155191	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs374321443	chr10:96155203-96155204	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs547021005	chr10:96155204-96155205	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs567129197	chr10:96155205-96155206	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs535700885	chr10:96155257-96155258	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs145272263	chr10:96155259-96155260	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs78470690	chr10:96155378-96155379	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs537500672	chr10:96155401-96155402	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs557338670	chr10:96155410-96155411	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs577606380	chr10:96155444-96155445	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs137927078	chr10:96155454-96155455	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs115615845	chr10:96155458-96155459	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs74153321	chr10:96155460-96155461	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs77306152	chr10:96155461-96155462	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs548751685	chr10:96155474-96155475	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs562644934	chr10:96155501-96155502	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs190563082	chr10:96155503-96155504	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Intracranial aneurysm	16715129	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic cancer	17952125	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:260 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96143200-96155400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:96154400-96154600	Enhancers	HepG2	liver
3	chr10:96154600-96155000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:96155000-96155200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr10:96155200-96155800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr10:96155200-96155800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr10:96155200-96155800	Active TSS	HepG2	liver
8	chr10:96155400-96155800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr10:96155800-96156200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr10:96155800-96157200	Weak transcription	HepG2	liver
11	chr10:96155800-96161800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr10:96155800-96162000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr10:96156200-96156800	Enhancers	HSMM	muscle
14	chr10:96156400-96156600	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr10:96156600-96157200	Enhancers	Muscle Satellite Cultured Cells	--
16	chr10:96156800-96158000	Weak transcription	HSMM	muscle
17	chr10:96157200-96157600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
18	chr10:96157200-96157600	Enhancers	Placenta	Placenta
19	chr10:96157200-96158200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr10:96157200-96158200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr10:96157200-96158200	Enhancers	HepG2	liver
22	chr10:96157400-96157600	Active TSS	A549	lung
23	chr10:96157400-96157800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr10:96157400-96157800	Enhancers	NH-A	brain
25	chr10:96157400-96157800	Enhancers	NHEK	skin
26	chr10:96157400-96158000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr10:96157400-96158200	Enhancers	K562	blood
28	chr10:96157400-96158400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr10:96157600-96157800	Enhancers	Muscle Satellite Cultured Cells	--
30	chr10:96157600-96157800	Flanking Active TSS	A549	lung
31	chr10:96157600-96158200	Enhancers	Hela-S3	cervix
32	chr10:96157600-96158200	Enhancers	HSMMtube	muscle
33	chr10:96157600-96161200	Weak transcription	Placenta	Placenta
34	chr10:96157800-96158000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
35	chr10:96157800-96158200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr10:96157800-96158200	Enhancers	A549	lung
37	chr10:96157800-96161800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr10:96157800-96161800	Weak transcription	NH-A	brain
39	chr10:96157800-96161800	Weak transcription	NHEK	skin
40	chr10:96158000-96158600	Enhancers	Muscle Satellite Cultured Cells	--
41	chr10:96158000-96158800	Enhancers	HSMM	muscle
42	chr10:96158000-96161800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr10:96158200-96161600	Weak transcription	Hela-S3	cervix
44	chr10:96158200-96161800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr10:96158200-96161800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr10:96158200-96161800	Weak transcription	A549	lung
47	chr10:96158200-96161800	Weak transcription	HepG2	liver
48	chr10:96158200-96161800	Weak transcription	HSMMtube	muscle
49	chr10:96158200-96161800	Weak transcription	K562	blood
50	chr10:96158400-96161800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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