Variant report

Variant	nsv551876
Chromosome Location	chr10:91704474-91735093
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	ATF2	chr10:91719469-91719945	GM12878	blood:	n/a	n/a
2	BATF	chr10:91714636-91715272	GM12878	blood:	n/a	n/a
3	BATF	chr10:91719496-91719906	GM12878	blood:	n/a	n/a
4	BATF	chr10:91719389-91719943	GM12878	blood:	n/a	n/a
5	BCL11A	chr10:91719406-91719973	GM12878	blood:	n/a	chr10:91719732-91719741
6	BCL11A	chr10:91719240-91719880	GM12878	blood:	n/a	chr10:91719377-91719386 chr10:91719732-91719741
7	CEBPB	chr10:91707746-91708068	A549	lung:	n/a	chr10:91707878-91707889
8	CEBPB	chr10:91717719-91717919	IMR90	lung:	n/a	chr10:91717835-91717846
9	CEBPB	chr10:91717668-91718002	HepG2	liver:	n/a	chr10:91717835-91717846
10	CEBPB	chr10:91707750-91708023	IMR90	lung:	n/a	chr10:91707878-91707889
11	CEBPB	chr10:91707769-91708041	HepG2	liver:	n/a	chr10:91707878-91707889
12	CEBPB	chr10:91717700-91717924	A549	lung:	n/a	chr10:91717835-91717846
13	CTCF	chr10:91714640-91714790	AG10803	skin:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
14	CTCF	chr10:91714980-91715130	BJ	skin:	n/a	n/a
15	CTCF	chr10:91714580-91714730	HA-sp	spinal cord:	n/a	n/a
16	CTCF	chr10:91714580-91714730	HPF	lung:	n/a	n/a
17	CTCF	chr10:91714600-91714750	SK-N-SH_RA	brain:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
18	CTCF	chr10:91714460-91714610	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr10:91714580-91714730	SAEC	small airway:	n/a	n/a
20	CTCF	chr10:91714700-91714850	AG09309	skin:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
21	CTCF	chr10:91714343-91714509	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr10:91714720-91714870	HCM	heart:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
23	CTCF	chr10:91714674-91714795	GM10266	blood:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
24	CTCF	chr10:91714280-91714430	NHLF	lung:	n/a	n/a
25	CTCF	chr10:91714560-91714710	HVMF	connective:	n/a	n/a
26	CTCF	chr10:91714700-91714850	AG04450	lung:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
27	CTCF	chr10:91714668-91714781	K562	blood:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
28	CTCF	chr10:91714640-91714790	Hela-S3	cervix:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
29	CTCF	chr10:91714660-91714810	RPTEC	kidney:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
30	CTCF	chr10:91714500-91714650	GM12867	blood:	n/a	n/a
31	CTCF	chr10:91714580-91714730	GM12865	blood:	n/a	n/a
32	CTCF	chr10:91714600-91714750	Caco-2	colon:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
33	CTCF	chr10:91714300-91714450	GM12868	blood:	n/a	n/a
34	CTCF	chr10:91714700-91714850	GM12872	blood:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
35	CTCF	chr10:91714200-91714350	GM12873	blood:	n/a	n/a
36	CTCF	chr10:91714445-91714921	GM12878	blood:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
37	CTCF	chr10:91714740-91714890	Caco-2	colon:	n/a	n/a
38	CTCF	chr10:91714660-91714810	HCPEpiC	choroid plexus:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
39	CTCF	chr10:91714660-91714810	HCFaa	heart:	n/a	chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744 chr10:91714722-91714738
40	CTCF	chr10:91714980-91715130	AG09319	gingival:	n/a	n/a
41	CTCF	chr10:91714406-91714991	HCT-116	colon:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
42	CTCF	chr10:91714900-91715050	RPTEC	kidney:	n/a	n/a
43	CTCF	chr10:91714613-91714797	GM13977	blood:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
44	CTCF	chr10:91714660-91714810	GM12872	blood:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
45	CTCF	chr10:91714620-91714770	HCM	heart:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
46	CTCF	chr10:91714340-91714490	SAEC	small airway:	n/a	n/a
47	CTCF	chr10:91714620-91714770	RPTEC	kidney:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
48	CTCF	chr10:91714720-91714870	HVMF	connective:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
49	CTCF	chr10:91714605-91714835	Medullo	brain:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
50	CTCF	chr10:91714646-91714856	K562	blood:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:91717815-91717865	HMEC	breast:	n/a
2	chr10:91717815-91717865	HUVEC	blood vessel:	n/a
3	chr10:91717815-91717865	NT2-D1	testis:	n/a
4	chr10:91717815-91717865	T-47D	breast:	n/a
5	chr10:91717815-91717865	Hela-S3	cervix:	n/a
6	chr10:91717815-91717865	HCPEpiC	choroid plexus:	n/a
7	chr10:91717815-91717865	ovcar-3	ovarian:	n/a
8	chr10:91717815-91717865	K562	blood:	n/a
9	chr10:91717815-91717865	HRCEpiC	kidney:	n/a
10	chr10:91717815-91717865	SKMC	muscle:	n/a
11	chr10:91717815-91717865	LNCaP	prostate:	n/a
12	chr10:91717815-91717865	BJ	skin:	n/a
13	chr10:91717815-91717865	HepG2	liver:	n/a
14	chr10:91717815-91717865	AG10803	skin:	n/a
15	chr10:91717815-91717865	HRE	kidney:	n/a
16	chr10:91717815-91717865	Caco-2	colon:	n/a
17	chr10:91717815-91717865	CMK	blood:	n/a
18	chr10:91717815-91717865	SK-N-SH	brain:	n/a
19	chr10:91717815-91717865	SK-N-SH_RA	brain:	n/a
20	chr10:91717815-91717865	GM12891	blood:	n/a
21	chr10:91717815-91717865	AG09309	skin:	n/a
22	chr10:91717815-91717865	AG09319	gingival:	n/a
23	chr10:91717815-91717865	HNPCEpiC	eye:	n/a
24	chr10:91717815-91717865	HCT-116	colon:	n/a
25	chr10:91717815-91717865	AoSMC	blood vessel:	n/a
26	chr10:91717815-91717865	GM19239	blood:	n/a
27	chr10:91717815-91717865	IMR90	lung:	fetal
28	chr10:91717815-91717865	SAEC	small airway:	n/a
29	chr10:91717815-91717865	RPTEC	kidney:	n/a
30	chr10:91717815-91717865	PANC-1	pancreas:	n/a
31	chr10:91717815-91717865	MCF10A-Er-Src	breast:	n/a
32	chr10:91717815-91717865	NB4	blood:	n/a
33	chr10:91717815-91717865	GM12878	blood:	n/a
34	chr10:91717815-91717865	Hepatocyte	liver:	n/a
35	chr10:91717815-91717865	H1-hESC	embryonic stem cell:	embryo
36	chr10:91717815-91717865	A549	lung:	n/a
37	chr10:91717815-91717865	PFSK-1	brain:	n/a
38	chr10:91717815-91717865	HL-60	blood:	n/a
39	chr10:91717815-91717865	HPAEpiC	pulmonary alveolar:	n/a
40	chr10:91717815-91717865	NHDF-neo	bronchial:	n/a
41	chr10:91717815-91717865	BE2_C	brain:	n/a
42	chr10:91717815-91717865	AG04449	skin:	fetal
43	chr10:91717815-91717865	HAEpiC	amniotic membrane:	n/a
44	chr10:91717815-91717865	HCM	heart:	n/a
45	chr10:91717815-91717865	HRPEpiC	eye:	n/a
46	chr10:91717815-91717865	AG04450	lung:	fetal
47	chr10:91717815-91717865	NHBE	bronchial:	n/a
48	chr10:91717815-91717865	HEEpiC	esophagus:	n/a
49	chr10:91717815-91717865	ProgFib	skin:	n/a
50	chr10:91717815-91717865	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:91722915..91725484-chr10:91726332..91728860,2	MCF-7	breast:
2	chr10:91718660..91720369-chr10:91722902..91725645,2	MCF-7	breast:
3	chr10:91722915..91725484-chr10:91726332..91728860,2	MCF-7	breast:
4	chr10:91718660..91720369-chr10:91722902..91725645,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PANK1-7	chr10:91706886-91707110	NONHSAT015579
2	lnc-PANK1-4	chr10:91715632-91715760	XLOC_008900
3	lnc-PANK1-4	chr10:91716906-91717130	XLOC_008900
4	lnc-PANK1-4	chr10:91715972-91716194	XLOC_008900
5	lnc-PANK1-7	chr10:91705612-91705740	NONHSAT015579
6	lnc-PANK1-7	chr10:91705952-91706174	NONHSAT015579

Variant related genes	Relation type
SNRPD2P1	TF binding region
ENSG00000226159	TF binding region
SNRPD2P1	CpG island
ENSG00000226159	CpG island
TGFBR2	miRNA target sites
HMGA2	miRNA target sites

Extended variants
information (count: 938 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:938 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1324698	chr10:91704474-91704475	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs187321098	chr10:91704475-91704476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564527158	chr10:91704482-91704483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572174458	chr10:91704491-91704492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190179716	chr10:91704548-91704549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540980981	chr10:91704595-91704596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs71022588	chr10:91704608-91704609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561194725	chr10:91704614-91704615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147052618	chr10:91704615-91704616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549805034	chr10:91704727-91704728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563329926	chr10:91704739-91704740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138307426	chr10:91704756-91704757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369324048	chr10:91704790-91704791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1924706	chr10:91704812-91704813	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs566157783	chr10:91704813-91704814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183054024	chr10:91704819-91704820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1924707	chr10:91704850-91704851	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs548437037	chr10:91704931-91704932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143789851	chr10:91704946-91704947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568170654	chr10:91704967-91704968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs117355878	chr10:91704987-91704988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556229053	chr10:91705002-91705003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs372161143	chr10:91705074-91705075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146357022	chr10:91705158-91705159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs58848913	chr10:91705165-91705166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144338541	chr10:91705189-91705190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs56703504	chr10:91705190-91705191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541172223	chr10:91705199-91705200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201636048	chr10:91705241-91705242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs397771991	chr10:91705255-91705256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560919366	chr10:91705307-91705308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77961189	chr10:91705321-91705322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs187620381	chr10:91705378-91705379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149426970	chr10:91705404-91705405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563366682	chr10:91705544-91705545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs532339653	chr10:91705561-91705562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs552400159	chr10:91705575-91705576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559752925	chr10:91705588-91705589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs113247670	chr10:91705649-91705650	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs76137222	chr10:91705684-91705685	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs548803755	chr10:91705706-91705707	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs144801820	chr10:91705779-91705780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372145235	chr10:91705786-91705787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551267273	chr10:91705832-91705833	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs80059117	chr10:91705836-91705837	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs569682564	chr10:91705847-91705848	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs538596075	chr10:91705910-91705911	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs148552738	chr10:91705932-91705933	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs184333699	chr10:91705952-91705953	Active TSS Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
50	rs187999237	chr10:91705955-91705956	Active TSS Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	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
Sezary syndrome	18413736	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91700200-91705600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr10:91703800-91704600	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr10:91704600-91705000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr10:91705000-91706000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr10:91705200-91706000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr10:91705200-91706200	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr10:91705400-91706000	Enhancers	Primary B cells from peripheral blood	blood
8	chr10:91705400-91706000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr10:91705400-91706400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr10:91705600-91706000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr10:91705800-91706200	Enhancers	Primary T cells from cord blood	blood
12	chr10:91705800-91706200	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr10:91705800-91706200	Flanking Active TSS	Dnd41	blood
14	chr10:91705800-91706200	Active TSS	NHDF-Ad	bronchial
15	chr10:91705800-91706200	Active TSS	NHLF	lung
16	chr10:91705800-91706400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr10:91706200-91706400	Enhancers	Dnd41	blood
18	chr10:91708600-91710200	Enhancers	Fetal Brain Male	brain
19	chr10:91709600-91713000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr10:91710200-91712000	Weak transcription	Fetal Brain Male	brain
21	chr10:91711600-91712000	ZNF genes & repeats	Fetal Stomach	stomach
22	chr10:91712000-91712400	Enhancers	Fetal Brain Male	brain
23	chr10:91712000-91713800	Weak transcription	Fetal Stomach	stomach
24	chr10:91712400-91713600	Weak transcription	Fetal Brain Male	brain
25	chr10:91712400-91714200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr10:91713600-91714200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr10:91713600-91714200	Enhancers	Fetal Brain Female	brain
28	chr10:91713600-91714400	Enhancers	Fetal Brain Male	brain
29	chr10:91713800-91714000	Enhancers	Right Atrium	heart
30	chr10:91713800-91714600	Enhancers	Fetal Stomach	stomach
31	chr10:91714200-91714400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr10:91714200-91714400	Enhancers	HMEC	breast
33	chr10:91714400-91715400	Enhancers	GM12878-XiMat	blood
34	chr10:91714400-91722600	Weak transcription	HMEC	breast
35	chr10:91715400-91718800	Weak transcription	GM12878-XiMat	blood
36	chr10:91717800-91718200	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr10:91718600-91725600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr10:91718800-91719600	Enhancers	Primary B cells from peripheral blood	blood
39	chr10:91718800-91720400	ZNF genes & repeats	GM12878-XiMat	blood
40	chr10:91719600-91719800	Enhancers	Primary B cells from cord blood	blood
41	chr10:91719800-91720000	Enhancers	NHEK	skin
42	chr10:91719800-91739800	Weak transcription	Primary B cells from cord blood	blood
43	chr10:91721800-91724400	Enhancers	NHEK	skin
44	chr10:91722000-91723200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr10:91722000-91723800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr10:91722400-91722800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr10:91722600-91724400	Enhancers	HMEC	breast
48	chr10:91724000-91741000	Weak transcription	Aorta	Aorta
49	chr10:91725600-91726400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr10:91725600-91727200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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