Variant report

Variant	esv2761585
Chromosome Location	chr10:27010701-27026012
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	chr10:27022975-27023447	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:27015086-27015416	HepG2	liver:	n/a	n/a
3	BACH1	chr10:27015297-27015497	K562	blood:	n/a	n/a
4	BCLAF1	chr10:27025917-27026410	GM12878	blood:	n/a	n/a
5	BHLHE40	chr10:27023003-27023487	HepG2	liver:	n/a	n/a
6	BHLHE40	chr10:27015064-27015371	GM12878	blood:	n/a	n/a
7	CEBPB	chr10:27022903-27023383	HepG2	liver:	n/a	n/a
8	CHD2	chr10:27023078-27023477	HepG2	liver:	n/a	n/a
9	CTCF	chr10:27015093-27015352	Hela-S3	cervix:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
10	CTCF	chr10:27017980-27018130	GM12865	blood:	n/a	n/a
11	CTCF	chr10:27018040-27018190	GM12870	blood:	n/a	n/a
12	CTCF	chr10:27015240-27015390	HA-sp	spinal cord:	n/a	n/a
13	CTCF	chr10:27018060-27018210	HAc	cerebellar:	n/a	n/a
14	CTCF	chr10:27015501-27015525	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr10:27015140-27015290	GM12872	blood:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
16	CTCF	chr10:27015120-27015270	WERI-Rb-1	eye:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
17	CTCF	chr10:27018040-27018190	GM12874	blood:	n/a	n/a
18	CTCF	chr10:27018040-27018137	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr10:27018048-27018105	K562	blood:	n/a	n/a
20	CTCF	chr10:27017980-27018130	GM12864	blood:	n/a	n/a
21	CTCF	chr10:27015120-27015270	AG09309	skin:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
22	CTCF	chr10:27015098-27015351	LNCaP	prostate:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
23	CTCF	chr10:27025420-27025570	GM12878	blood:	n/a	n/a
24	CTCF	chr10:27018020-27018170	HCT-116	colon:	n/a	n/a
25	CTCF	chr10:27015140-27015290	K562	blood:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
26	CTCF	chr10:27018017-27018019	GM19240	blood:	n/a	n/a
27	CTCF	chr10:27015120-27015270	SAEC	small airway:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
28	CTCF	chr10:27015122-27015321	GM13976	blood:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
29	CTCF	chr10:27015090-27015346	Kidney_OC	kidney:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
30	CTCF	chr10:27015120-27015270	BJ	skin:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
31	CTCF	chr10:27018020-27018170	GM12868	blood:	n/a	n/a
32	CTCF	chr10:27014911-27014968	GM19238	blood:	n/a	n/a
33	CTCF	chr10:27015107-27015335	GM10266	blood:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
34	CTCF	chr10:27018000-27018150	MCF-7	breast:	n/a	n/a
35	CTCF	chr10:27015136-27015281	GM12891	blood:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
36	CTCF	chr10:27017980-27018130	BJ	skin:	n/a	n/a
37	CTCF	chr10:27018060-27018210	GM12869	blood:	n/a	n/a
38	CTCF	chr10:27014904-27014986	GM12891	blood:	n/a	n/a
39	CTCF	chr10:27018020-27018170	HMF	breast:	n/a	n/a
40	CTCF	chr10:27015140-27015290	HPF	lung:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
41	CTCF	chr10:27015140-27015290	GM12801	blood:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
42	CTCF	chr10:27015160-27015310	GM12872	blood:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
43	CTCF	chr10:27017960-27018110	GM12866	blood:	n/a	n/a
44	CTCF	chr10:27015140-27015290	AG04449	skin:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
45	CTCF	chr10:27014990-27015369	HepG2	liver:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
46	CTCF	chr10:27015060-27015210	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr10:27015140-27015290	HCPEpiC	choroid plexus:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
48	CTCF	chr10:27015180-27015330	BE2_C	brain:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231
49	CTCF	chr10:27014520-27014670	AG09319	gingival:	n/a	n/a
50	CTCF	chr10:27015120-27015270	GM12868	blood:	n/a	chr10:27015216-27015225 chr10:27015214-27015230 chr10:27015215-27015236 chr10:27015213-27015231

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:27023190-27023240	SK-N-MC	brain:	n/a
2	chr10:27023190-27023240	SKMC	muscle:	n/a
3	chr10:27023190-27023240	Hela-S3	cervix:	n/a
4	chr10:27023190-27023240	A549	lung:	n/a
5	chr10:27023190-27023240	HCPEpiC	choroid plexus:	n/a
6	chr10:27023190-27023240	HEK293	kidney:	embryo
7	chr10:27023190-27023240	NHBE	bronchial:	n/a
8	chr10:27023190-27023240	HAEpiC	amniotic membrane:	n/a
9	chr10:27023190-27023240	GM19239	blood:	n/a
10	chr10:27023190-27023240	Hepatocyte	liver:	n/a
11	chr10:27023190-27023240	ECC-1	luminal epithelium:	n/a
12	chr10:27023190-27023240	RPTEC	kidney:	n/a
13	chr10:27023190-27023240	HEEpiC	esophagus:	n/a
14	chr10:27023190-27023240	HMEC	breast:	n/a
15	chr10:27023190-27023240	SK-N-SH_RA	brain:	n/a
16	chr10:27023190-27023240	AoSMC	blood vessel:	n/a
17	chr10:27023190-27023240	HCM	heart:	n/a
18	chr10:27023190-27023240	T-47D	breast:	n/a
19	chr10:27023190-27023240	HIPEpiC	eye:	n/a
20	chr10:27023190-27023240	GM12891	blood:	n/a
21	chr10:27023190-27023240	AG09309	skin:	n/a
22	chr10:27023190-27023240	IMR90	lung:	fetal
23	chr10:27023190-27023240	Caco-2	colon:	n/a
24	chr10:27023190-27023240	ProgFib	skin:	n/a
25	chr10:27023190-27023240	MCF-7	breast:	n/a
26	chr10:27023190-27023240	AG09319	gingival:	n/a
27	chr10:27023190-27023240	BE2_C	brain:	n/a
28	chr10:27023190-27023240	ovcar-3	ovarian:	n/a
29	chr10:27023190-27023240	GM06990	blood:	n/a
30	chr10:27023190-27023240	HRPEpiC	eye:	n/a
31	chr10:27023190-27023240	AG04450	lung:	fetal
32	chr10:27023190-27023240	BJ	skin:	n/a
33	chr10:27023190-27023240	HCF	heart:	n/a
34	chr10:27023190-27023240	PrEC	prostate:	n/a
35	chr10:27023190-27023240	GM12892	blood:	n/a
36	chr10:27023190-27023240	PANC-1	pancreas:	n/a
37	chr10:27023190-27023240	SK-N-SH	brain:	n/a
38	chr10:27023190-27023240	PFSK-1	brain:	n/a
39	chr10:27023190-27023240	Jurkat	blood:	n/a
40	chr10:27023190-27023240	CMK	blood:	n/a
41	chr10:27023190-27023240	NB4	blood:	n/a
42	chr10:27023190-27023240	H1-hESC	embryonic stem cell:	embryo
43	chr10:27023190-27023240	HNPCEpiC	eye:	n/a
44	chr10:27023190-27023240	HL-60	blood:	n/a
45	chr10:27023190-27023240	AG10803	skin:	n/a
46	chr10:27023190-27023240	HepG2	liver:	n/a
47	chr10:27023190-27023240	HUVEC	blood vessel:	n/a
48	chr10:27023190-27023240	HRE	kidney:	n/a
49	chr10:27023190-27023240	HPAEpiC	pulmonary alveolar:	n/a
50	chr10:27023190-27023240	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:27007355..27009512-chr10:27013703..27015717,2	K562	blood:
2	chr10:26986198..26989615-chr10:27022506..27024765,3	MCF-7	breast:
3	chr10:27018097..27019836-chr10:27021900..27023987,2	K562	blood:
4	chr10:27014809..27015628-chr10:27170414..27171655,4	MCF-7	breast:
5	chr10:27020372..27021992-chr10:27022425..27024329,2	K562	blood:
6	chr10:27023145..27024775-chr10:27148207..27150009,2	MCF-7	breast:
7	chr10:27025829..27027714-chr10:27034224..27036690,2	K562	blood:
8	chr10:27020685..27022973-chr10:27138065..27140730,2	MCF-7	breast:
9	chr10:27015169..27015701-chr10:27150108..27150645,2	K562	blood:
10	chr10:26995580..26998397-chr10:27011031..27013187,2	K562	blood:
11	chr10:27021769..27024487-chr10:27025827..27029432,3	MCF-7	breast:
12	chr10:27014360..27015711-chr10:27170641..27171581,4	K562	blood:
13	chr10:27009604..27012083-chr10:27443909..27445866,2	K562	blood:
14	chr10:27019861..27021992-chr10:27022425..27025039,2	K562	blood:

Variant related genes	Relation type
PDSS1	TF binding region
PDSS1	CpG island
ENSG00000136754	chromatin interactions
ENSG00000148459	chromatin interactions
ENSG00000136758	chromatin interactions
ENSG00000120539	chromatin interactions

Extended variants
information (count: 662 )
Associated
traits (count: 42 )

Variant overlapped rSNPs/rCNVs (count:662 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568947430	chr10:27010722-27010723	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs374836739	chr10:27010729-27010730	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs112174950	chr10:27010730-27010731	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs567452614	chr10:27010737-27010738	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs112900162	chr10:27010750-27010751	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs115216018	chr10:27010763-27010764	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs571351462	chr10:27010773-27010774	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs183053295	chr10:27010832-27010833	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs377602327	chr10:27010882-27010883	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs370974242	chr10:27010897-27010898	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs553971607	chr10:27010898-27010899	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs188093917	chr10:27010914-27010915	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs539546201	chr10:27010932-27010933	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs556179821	chr10:27010961-27010962	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs533926178	chr10:27010967-27010968	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs190784609	chr10:27010982-27010983	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs373721767	chr10:27011014-27011015	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs147432005	chr10:27011040-27011041	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs369444270	chr10:27011071-27011072	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs574036062	chr10:27011076-27011077	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs540468009	chr10:27011077-27011078	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs1564271	chr10:27011112-27011113	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs532486959	chr10:27011132-27011133	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs545911915	chr10:27011136-27011137	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs562511992	chr10:27011216-27011217	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs182474623	chr10:27011226-27011227	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs2489551	chr10:27011296-27011297	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs2477301	chr10:27011323-27011324	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs527629150	chr10:27011349-27011350	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs1985337	chr10:27011352-27011353	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs2489550	chr10:27011355-27011356	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs139730065	chr10:27011371-27011372	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs372284463	chr10:27011372-27011373	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs367660418	chr10:27011398-27011399	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs569630575	chr10:27011400-27011401	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs368519057	chr10:27011420-27011421	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs570216846	chr10:27011421-27011422	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs577715666	chr10:27011437-27011438	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs540195166	chr10:27011506-27011507	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs35382920	chr10:27011523-27011524	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs143650988	chr10:27011564-27011565	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs575012293	chr10:27011581-27011582	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs113869991	chr10:27011626-27011627	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs549381382	chr10:27011673-27011674	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs554041823	chr10:27011689-27011690	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs72792175	chr10:27011747-27011748	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs78852105	chr10:27011818-27011819	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs11015249	chr10:27011863-27011864	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs562739368	chr10:27011907-27011908	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs541816453	chr10:27011911-27011912	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:42)

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

Chromatin state (count:705 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26987600-27024400	Weak transcription	Fetal Kidney	kidney
2	chr10:26987800-27010800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr10:26987800-27020400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr10:26987800-27031200	Weak transcription	NHDF-Ad	bronchial
5	chr10:26988000-27069600	Weak transcription	Colon Smooth Muscle	Colon
6	chr10:26989400-27031000	Weak transcription	Small Intestine	intestine
7	chr10:26994400-27040800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr10:26995400-27023000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr10:26995800-27026600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr10:26996000-27026600	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr10:26996200-27026200	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr10:26996200-27028000	Weak transcription	Psoas Muscle	Psoas
13	chr10:26996600-27012000	Weak transcription	Brain Cingulate Gyrus	brain
14	chr10:26996600-27022400	Weak transcription	Brain Angular Gyrus	brain
15	chr10:26996600-27023600	Weak transcription	Fetal Heart	heart
16	chr10:26997200-27012200	Weak transcription	HSMM	muscle
17	chr10:26997200-27022800	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr10:26997200-27024400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr10:26997400-27022400	Weak transcription	Brain Substantia Nigra	brain
20	chr10:26997600-27012800	Weak transcription	Brain Hippocampus Middle	brain
21	chr10:26997600-27054400	Weak transcription	Fetal Brain Male	brain
22	chr10:26998000-27010800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr10:26998000-27011800	Weak transcription	Rectal Smooth Muscle	rectum
24	chr10:26998000-27022400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr10:26998200-27015000	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr10:26998200-27015400	Weak transcription	Brain Anterior Caudate	brain
27	chr10:26998200-27022400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr10:26998600-27012200	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr10:26999800-27022600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr10:26999800-27037400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr10:27000800-27010800	Weak transcription	Ovary	ovary
32	chr10:27001000-27031800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr10:27001200-27041200	Strong transcription	Fetal Thymus	thymus
34	chr10:27001800-27041200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr10:27002200-27015200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
36	chr10:27002200-27017000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr10:27002200-27021600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr10:27002200-27023400	Strong transcription	HUES64 Cell Line	embryonic stem cell
39	chr10:27002400-27017200	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr10:27003600-27014600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr10:27004200-27011800	Weak transcription	Osteobl	bone
42	chr10:27004200-27012400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr10:27004200-27031200	Weak transcription	Hela-S3	cervix
44	chr10:27004400-27016200	Weak transcription	Fetal Lung	lung
45	chr10:27004400-27022800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr10:27004600-27014600	Weak transcription	Colonic Mucosa	Colon
47	chr10:27005200-27012800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr10:27005200-27013600	Weak transcription	Placenta	Placenta
49	chr10:27005400-27012800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr10:27005400-27013600	Weak transcription	Skeletal Muscle Male	skeletal muscle

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