Variant report

Variant	nsv894816
Chromosome Location	chr10:6173416-6190343
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:817)
CpG islands
(count:1160)
Chromatin interactive
region (count:39)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:6186478-6186567	HepG2	liver:	n/a	n/a
2	ATF2	chr10:6177071-6177439	GM12878	blood:	n/a	n/a
3	ATF2	chr10:6182997-6184150	GM12878	blood:	n/a	n/a
4	ATF2	chr10:6178156-6178687	GM12878	blood:	n/a	n/a
5	ATF2	chr10:6178131-6178750	GM12878	blood:	n/a	n/a
6	ATF2	chr10:6182908-6184226	GM12878	blood:	n/a	n/a
7	BACH1	chr10:6183401-6183628	K562	blood:	n/a	n/a
8	BACH1	chr10:6186441-6187396	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:6182144-6182201	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr10:6183032-6183954	GM12878	blood:	n/a	n/a
11	BATF	chr10:6178125-6178927	GM12878	blood:	n/a	n/a
12	BATF	chr10:6182368-6184471	GM12878	blood:	n/a	n/a
13	BATF	chr10:6178273-6178653	GM12878	blood:	n/a	n/a
14	BCL11A	chr10:6178274-6178551	GM12878	blood:	n/a	n/a
15	BCL11A	chr10:6178175-6178638	GM12878	blood:	n/a	n/a
16	BCL11A	chr10:6182829-6184316	GM12878	blood:	n/a	n/a
17	BCL11A	chr10:6183141-6183473	GM12878	blood:	n/a	n/a
18	BCL3	chr10:6183637-6184202	GM12878	blood:	n/a	n/a
19	BCL3	chr10:6183142-6183595	GM12878	blood:	n/a	n/a
20	BCL3	chr10:6180142-6180615	GM12878	blood:	n/a	n/a
21	BCL3	chr10:6177549-6177922	GM12878	blood:	n/a	n/a
22	BCLAF1	chr10:6178164-6178905	GM12878	blood:	n/a	n/a
23	BCLAF1	chr10:6182798-6184187	GM12878	blood:	n/a	n/a
24	BCLAF1	chr10:6178149-6178789	GM12878	blood:	n/a	n/a
25	BCLAF1	chr10:6182993-6184166	GM12878	blood:	n/a	n/a
26	BCLAF1	chr10:6176869-6177456	GM12878	blood:	n/a	n/a
27	BHLHE40	chr10:6186498-6187468	GM12878	blood:	n/a	chr10:6186760-6186776 chr10:6186657-6186673
28	BHLHE40	chr10:6182477-6184159	GM12878	blood:	n/a	n/a
29	BHLHE40	chr10:6183178-6183969	K562	blood:	n/a	n/a
30	BHLHE40	chr10:6178195-6178854	GM12878	blood:	n/a	n/a
31	BHLHE40	chr10:6186490-6187519	K562	blood:	n/a	chr10:6186760-6186776 chr10:6186657-6186673
32	BRCA1	chr10:6188570-6188651	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr10:6185884-6185887	GM12878	blood:	n/a	n/a
34	BRCA1	chr10:6187147-6187150	GM12878	blood:	n/a	n/a
35	CBX3	chr10:6186571-6186944	K562	blood:	n/a	n/a
36	CBX3	chr10:6187091-6187533	K562	blood:	n/a	n/a
37	CBX3	chr10:6183360-6183705	K562	blood:	n/a	n/a
38	CCNT2	chr10:6186488-6187503	K562	blood:	n/a	n/a
39	CEBPB	chr10:6186364-6186477	IMR90	lung:	n/a	chr10:6186415-6186426 chr10:6186415-6186424
40	CEBPB	chr10:6183059-6183608	IMR90	lung:	n/a	n/a
41	CEBPB	chr10:6185374-6185490	HepG2	liver:	n/a	n/a
42	CEBPB	chr10:6183069-6183922	GM12878	blood:	n/a	n/a
43	CEBPB	chr10:6185728-6185928	HepG2	liver:	n/a	n/a
44	CEBPB	chr10:6185290-6185467	K562	blood:	n/a	n/a
45	CHD1	chr10:6186448-6186449	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr10:6186896-6187320	GM12878	blood:	n/a	n/a
47	CHD1	chr10:6182327-6184009	GM12878	blood:	n/a	n/a
48	CHD1	chr10:6186295-6188964	IMR90	lung:	n/a	n/a
49	CHD1	chr10:6182777-6184233	IMR90	lung:	n/a	n/a
50	CHD2	chr10:6178226-6178945	GM12878	blood:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:6186637-6186687	MCF10A-Er-Src	breast:	n/a
2	chr10:6186637-6186687	MCF10A-Er-Src	breast:	n/a
3	chr10:6186668-6186718	Jurkat	blood:	n/a
4	chr10:6186663-6186713	T-47D	breast:	n/a
5	chr10:6186637-6186687	LNCaP	prostate:	n/a
6	chr10:6189073-6189123	SAEC	small airway:	n/a
7	chr10:6187284-6187334	GM12878	blood:	n/a
8	chr10:6187854-6187904	T-47D	breast:	n/a
9	chr10:6183872-6183922	MCF10A-Er-Src	breast:	n/a
10	chr10:6185933-6185983	Jurkat	blood:	n/a
11	chr10:6185933-6185983	IMR90	lung:	fetal
12	chr10:6186649-6186699	T-47D	breast:	n/a
13	chr10:6178319-6178369	LNCaP	prostate:	n/a
14	chr10:6189073-6189123	MCF-7	breast:	n/a
15	chr10:6186649-6186699	AG10803	skin:	n/a
16	chr10:6186668-6186718	MCF10A-Er-Src	breast:	n/a
17	chr10:6186668-6186718	HCM	heart:	n/a
18	chr10:6187854-6187904	RPTEC	kidney:	n/a
19	chr10:6189073-6189123	SKMC	muscle:	n/a
20	chr10:6186649-6186699	LNCaP	prostate:	n/a
21	chr10:6187284-6187334	GM19239	blood:	n/a
22	chr10:6183528-6183578	HMEC	breast:	n/a
23	chr10:6185933-6185983	NHDF-neo	bronchial:	n/a
24	chr10:6186959-6187009	CMK	blood:	n/a
25	chr10:6178319-6178369	RPTEC	kidney:	n/a
26	chr10:6186649-6186699	H1-hESC	embryonic stem cell:	embryo
27	chr10:6183575-6183625	PrEC	prostate:	n/a
28	chr10:6186794-6186844	HPAEpiC	pulmonary alveolar:	n/a
29	chr10:6186649-6186699	SAEC	small airway:	n/a
30	chr10:6186668-6186718	K562	blood:	n/a
31	chr10:6186668-6186718	AG04450	lung:	fetal
32	chr10:6183455-6183505	NT2-D1	testis:	n/a
33	chr10:6186668-6186718	AG09309	skin:	n/a
34	chr10:6186668-6186718	GM12878	blood:	n/a
35	chr10:6178319-6178369	BE2_C	brain:	n/a
36	chr10:6183528-6183578	AG09319	gingival:	n/a
37	chr10:6183872-6183922	ProgFib	skin:	n/a
38	chr10:6183575-6183625	AG10803	skin:	n/a
39	chr10:6187284-6187334	RPTEC	kidney:	n/a
40	chr10:6186959-6187009	BE2_C	brain:	n/a
41	chr10:6185933-6185983	HCT-116	colon:	n/a
42	chr10:6186668-6186718	T-47D	breast:	n/a
43	chr10:6186647-6186697	Hepatocyte	liver:	n/a
44	chr10:6186794-6186844	PFSK-1	brain:	n/a
45	chr10:6186959-6187009	NH-A	brain:	n/a
46	chr10:6186794-6186844	K562	blood:	n/a
47	chr10:6186542-6186592	HRPEpiC	eye:	n/a
48	chr10:6187854-6187904	SKMC	muscle:	n/a
49	chr10:6187284-6187334	MCF-7	breast:	n/a
50	chr10:6186637-6186687	SAEC	small airway:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:6182309..6185774-chr10:6185942..6188983,5	MCF-7	breast:
2	chr10:6185856..6188791-chr10:6189568..6196117,9	MCF-7	breast:
3	chr10:6130589..6132639-chr10:6184439..6189476,5	K562	blood:
4	chr10:6183938..6190482-chr10:6242008..6247032,17	MCF-7	breast:
5	chr10:6175966..6181179-chr10:6182519..6187998,8	K562	blood:
6	chr10:6179137..6182411-chr10:6242546..6245142,3	MCF-7	breast:
7	chr10:6060947..6063701-chr10:6181512..6183483,2	K562	blood:
8	chr10:6186975..6187599-chr11:61734610..61735476,2	Hela-S3	cervix:
9	chr10:6131173..6133943-chr10:6186718..6189110,2	MCF-7	breast:
10	chr10:6164842..6170645-chr10:6170879..6175262,7	K562	blood:
11	chr10:6175564..6180792-chr10:6183747..6189034,7	MCF-7	breast:
12	chr10:6157377..6159891-chr10:6179224..6181720,2	MCF-7	breast:
13	chr10:6186531..6187074-chr10:6244769..6245442,2	MCF-7	breast:
14	chr10:6181525..6183322-chr10:6221078..6223708,2	MCF-7	breast:
15	chr10:6178646..6179311-chr5:179268532..179269425,2	MCF-7	breast:
16	chr10:6188903..6191152-chr10:6204778..6206877,2	MCF-7	breast:
17	chr10:6148307..6150480-chr10:6188512..6190404,2	MCF-7	breast:
18	chr10:6150598..6153044-chr10:6184117..6186836,2	K562	blood:
19	chr10:6189894..6192661-chr10:6244759..6246996,2	MCF-7	breast:
20	chr10:6183735..6189299-chr10:6241759..6246920,10	MCF-7	breast:
21	chr10:6155651..6158898-chr10:6185032..6187374,4	MCF-7	breast:
22	chr10:6171306..6174580-chr10:6176089..6182503,5	MCF-7	breast:
23	chr10:6149255..6151858-chr10:6188263..6190070,3	K562	blood:
24	chr10:6185856..6188791-chr10:6189568..6196117,9	MCF-7	breast:
25	chr10:6171306..6174580-chr10:6176089..6182503,5	MCF-7	breast:
26	chr10:6161419..6164207-chr10:6176225..6178113,3	MCF-7	breast:
27	chr10:6182985..6185643-chr10:6203385..6205220,2	K562	blood:
28	chr10:6171733..6174384-chr10:6244716..6246258,2	MCF-7	breast:
29	chr10:6180971..6185195-chr10:6203384..6207419,4	MCF-7	breast:
30	chr10:6130591..6133050-chr10:6185385..6187497,2	MCF-7	breast:
31	chr10:6176204..6177966-chr10:6243540..6246066,2	MCF-7	breast:
32	chr10:6171947..6174676-chr10:6182111..6184339,3	MCF-7	breast:
33	chr10:6176060..6177647-chr10:6211821..6213802,2	MCF-7	breast:
34	chr10:6178289..6180326-chr10:6204239..6205826,2	K562	blood:
35	chr10:6186815..6187427-chr6:136610849..136611598,2	HCT-116	colon:
36	chr10:5930398..5933295-chr10:6184026..6187985,3	K562	blood:
37	chr10:6166112..6169238-chr10:6173042..6175733,3	K562	blood:
38	chr10:6186819..6188569-chr6:44214871..44216412,2	K562	blood:
39	chr10:6171947..6174676-chr10:6182111..6184339,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PFKFB3-1	chr10:6182721-6182750	XLOC_008366
2	lnc-IL2RA-2	chr10:6179496-6179520	ENSG00000232547.1
3	lnc-IL2RA-2	chr10:6178277-6178403	ENSG00000232547.1
4	lnc-PFKFB3-1	chr10:6183050-6183545	XLOC_008366

No data

Variant related genes	Relation type
MIR3155A	TF binding region
RN7SKP78	TF binding region
PFKFB3	TF binding region
MIR3155A	CpG island
RN7SKP78	CpG island
PFKFB3	CpG island
ENSG00000170525	chromatin interactions
ENSG00000167996	chromatin interactions
ENSG00000134453	chromatin interactions
ENSG00000201581	chromatin interactions
ENSG00000134452	chromatin interactions
ENSG00000213994	chromatin interactions
ENSG00000269089	chromatin interactions
ENSG00000029363	chromatin interactions
ENSG00000134461	chromatin interactions
ENSG00000263628	chromatin interactions
ENSG00000096384	chromatin interactions

Extended variants
information (count: 774 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:774 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7914915	chr10:6173416-6173417	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs367545250	chr10:6173431-6173432	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs554462184	chr10:6173443-6173444	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs535198873	chr10:6173450-6173451	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs11256933	chr10:6173465-6173466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs574835924	chr10:6173620-6173621	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs7924005	chr10:6173693-6173694	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs565125712	chr10:6173723-6173724	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs374379211	chr10:6173726-6173727	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs17150879	chr10:6173728-6173729	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs141297771	chr10:6173734-6173735	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs543772845	chr10:6173737-6173738	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs370090721	chr10:6173742-6173743	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs558530857	chr10:6173759-6173760	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs7087477	chr10:6173760-6173761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs372314182	chr10:6173776-6173777	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs10905875	chr10:6173777-6173778	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs192121268	chr10:6173797-6173798	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs566918622	chr10:6173816-6173817	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs146989245	chr10:6173935-6173936	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs548574934	chr10:6173936-6173937	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs61839702	chr10:6173963-6173964	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs575083738	chr10:6174003-6174004	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs368820897	chr10:6174004-6174005	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs569353770	chr10:6174018-6174019	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs112908415	chr10:6174020-6174021	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs116171295	chr10:6174033-6174034	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs374953258	chr10:6174107-6174108	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs552586719	chr10:6174214-6174215	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs535147493	chr10:6174240-6174241	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs552480913	chr10:6174242-6174243	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs548378097	chr10:6174345-6174346	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs571098199	chr10:6174346-6174347	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs7915363	chr10:6174356-6174357	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs79479742	chr10:6174369-6174370	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs35707936	chr10:6174387-6174388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs118093004	chr10:6174413-6174414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183890471	chr10:6174418-6174419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs71479757	chr10:6174432-6174433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535993152	chr10:6174462-6174463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557473350	chr10:6174474-6174475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372013656	chr10:6174475-6174476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539812185	chr10:6174481-6174482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537414831	chr10:6174502-6174503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs557689571	chr10:6174533-6174534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs28420903	chr10:6174562-6174563	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs539733630	chr10:6174570-6174571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577028538	chr10:6174573-6174574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553576469	chr10:6174574-6174575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540874429	chr10:6174585-6174586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
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
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Ovarian cancer	22355333	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1184 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:6167600-6174800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr10:6168200-6178200	Weak transcription	A549	lung
3	chr10:6170400-6173600	Enhancers	NH-A	brain
4	chr10:6171200-6173600	Enhancers	NHLF	lung
5	chr10:6171200-6174200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr10:6171200-6177000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr10:6171200-6178600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:6171400-6175200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr10:6171400-6183200	Weak transcription	Right Atrium	heart
10	chr10:6172200-6175600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr10:6172200-6175600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr10:6172200-6175600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr10:6172200-6176400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr10:6172200-6178400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr10:6172200-6178400	Weak transcription	Adipose Nuclei	Adipose
16	chr10:6172200-6182800	Weak transcription	Brain Angular Gyrus	brain
17	chr10:6172400-6173600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr10:6172400-6176200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr10:6172400-6176200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr10:6172400-6178200	Weak transcription	Esophagus	oesophagus
21	chr10:6172400-6181600	Weak transcription	Spleen	Spleen
22	chr10:6172400-6182200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr10:6172600-6176800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr10:6172800-6173600	Enhancers	NHDF-Ad	bronchial
25	chr10:6173000-6176200	Weak transcription	Fetal Thymus	thymus
26	chr10:6173000-6176800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr10:6173000-6181000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr10:6173200-6174400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr10:6173200-6175000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr10:6173200-6175600	Weak transcription	GM12878-XiMat	blood
31	chr10:6173200-6176400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr10:6173200-6176600	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr10:6173200-6178400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr10:6173400-6173600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr10:6173400-6176200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr10:6173400-6176800	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr10:6173400-6176800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr10:6173400-6178000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr10:6173400-6178000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr10:6173600-6174400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr10:6173600-6176600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr10:6173600-6177800	Weak transcription	NHDF-Ad	bronchial
43	chr10:6173600-6178000	Weak transcription	NH-A	brain
44	chr10:6173600-6178000	Weak transcription	NHLF	lung
45	chr10:6174200-6174400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr10:6174400-6176400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr10:6174400-6177000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr10:6174800-6175200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr10:6175000-6176800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
50	chr10:6175200-6175800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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