Variant report

Variant	nsv1037657
Chromosome Location	chr10:90329910-90367890
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	chr10:90342487-90343358	GM12878	blood:	n/a	n/a
2	ATF3	chr10:90342497-90342885	GM12878	blood:	n/a	chr10:90342650-90342670 chr10:90342661-90342670
3	ATF3	chr10:90342553-90342782	GM12878	blood:	n/a	chr10:90342650-90342670 chr10:90342661-90342670
4	ATF3	chr10:90342558-90342841	H1-hESC	embryonic stem cell:	n/a	chr10:90342650-90342670 chr10:90342661-90342670
5	ATF3	chr10:90342556-90342930	H1-hESC	embryonic stem cell:	n/a	chr10:90342650-90342670 chr10:90342661-90342670
6	BACH1	chr10:90342738-90343061	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr10:90367779-90368459	GM12878	blood:	n/a	n/a
8	BCLAF1	chr10:90342505-90343467	GM12878	blood:	n/a	chr10:90343114-90343127
9	BCLAF1	chr10:90357695-90358200	GM12878	blood:	n/a	n/a
10	BHLHE40	chr10:90343183-90343272	K562	blood:	n/a	n/a
11	BHLHE40	chr10:90342539-90342866	K562	blood:	n/a	chr10:90342661-90342670 chr10:90342661-90342670 chr10:90342659-90342672 chr10:90342662-90342671
12	BHLHE40	chr10:90342352-90343314	GM12878	blood:	n/a	chr10:90342661-90342670 chr10:90342661-90342670 chr10:90342659-90342672 chr10:90342662-90342671
13	CEBPB	chr10:90358937-90359032	A549	lung:	n/a	n/a
14	CHD1	chr10:90342766-90343148	GM12878	blood:	n/a	n/a
15	CHD1	chr10:90342031-90342069	GM12878	blood:	n/a	n/a
16	CHD2	chr10:90342562-90343360	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr10:90342545-90343324	GM12878	blood:	n/a	n/a
18	CREB1	chr10:90342512-90343170	A549	lung:	n/a	n/a
19	CREB1	chr10:90342484-90343348	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr10:90357784-90358402	GM12878	blood:	n/a	n/a
21	CREB1	chr10:90342493-90343248	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr10:90357833-90358294	GM12878	blood:	n/a	n/a
23	CTCF	chr10:90364621-90364636	GM20000	blood:	n/a	n/a
24	CTCF	chr10:90343000-90343150	GM12866	blood:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
25	CTCF	chr10:90343020-90343170	GM12875	blood:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
26	CTCF	chr10:90342032-90342065	GM10248	blood:	n/a	n/a
27	CTCF	chr10:90342680-90342830	AG04449	skin:	n/a	n/a
28	CTCF	chr10:90342970-90343217	GM13976	blood:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
29	CTCF	chr10:90342769-90343221	GM12878	blood:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
30	CTCF	chr10:90343011-90343174	HepG2	liver:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
31	CTCF	chr10:90342909-90343220	GM10248	blood:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
32	CTCF	chr10:90343040-90343190	HEEpiC	esophagus:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
33	CTCF	chr10:90343020-90343170	HMEC	breast:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
34	CTCF	chr10:90342660-90342810	GM12868	blood:	n/a	n/a
35	CTCF	chr10:90343022-90343168	K562	blood:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
36	CTCF	chr10:90342876-90343259	GM19239	blood:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
37	CTCF	chr10:90342740-90342890	A549	lung:	n/a	n/a
38	CTCF	chr10:90342660-90342810	GM12866	blood:	n/a	n/a
39	CTCF	chr10:90343000-90343150	GM12868	blood:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
40	CTCF	chr10:90342693-90343250	A549	lung:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
41	CTCF	chr10:90342900-90343266	HepG2	liver:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
42	CTCF	chr10:90342759-90342818	MCF-7	breast:	n/a	n/a
43	CTCF	chr10:90343020-90343170	HEEpiC	esophagus:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
44	CTCF	chr10:90342695-90343262	Gliobla	brain:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
45	CTCF	chr10:90342678-90342815	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr10:90343040-90343190	HepG2	liver:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
47	CTCF	chr10:90343020-90343170	HBMEC	blood vessel:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
48	CTCF	chr10:90343040-90343190	RPTEC	kidney:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
49	CTCF	chr10:90342917-90343225	Lung_OC	lung:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
50	CTCF	chr10:90343020-90343170	AoAF	blood vessel:	n/a	chr10:90343091-90343109 chr10:90343094-90343107

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:90345170-90345220	AG09319	gingival:	n/a
2	chr10:90345170-90345220	AG09319	gingival:	n/a
3	chr10:90345860-90345910	Caco-2	colon:	n/a
4	chr10:90345860-90345910	HRPEpiC	eye:	n/a
5	chr10:90343166-90343216	HCM	heart:	n/a
6	chr10:90346479-90346529	NHDF-neo	bronchial:	n/a
7	chr10:90346479-90346529	HepG2	liver:	n/a
8	chr10:90346597-90346647	AG10803	skin:	n/a
9	chr10:90346479-90346529	PANC-1	pancreas:	n/a
10	chr10:90345356-90345406	A549	lung:	n/a
11	chr10:90342899-90342949	GM06990	blood:	n/a
12	chr10:90343208-90343258	MCF10A-Er-Src	breast:	n/a
13	chr10:90364671-90364721	HRE	kidney:	n/a
14	chr10:90341959-90342009	BE2_C	brain:	n/a
15	chr10:90345356-90345406	AoSMC	blood vessel:	n/a
16	chr10:90339186-90339236	HNPCEpiC	eye:	n/a
17	chr10:90343192-90343242	K562	blood:	n/a
18	chr10:90342899-90342949	ProgFib	skin:	n/a
19	chr10:90345860-90345910	AoSMC	blood vessel:	n/a
20	chr10:90343435-90343485	BE2_C	brain:	n/a
21	chr10:90343285-90343335	HRCEpiC	kidney:	n/a
22	chr10:90343204-90343254	SK-N-SH_RA	brain:	n/a
23	chr10:90345356-90345406	MCF-7	breast:	n/a
24	chr10:90346479-90346529	SK-N-SH_RA	brain:	n/a
25	chr10:90345356-90345406	GM19239	blood:	n/a
26	chr10:90346479-90346529	HRPEpiC	eye:	n/a
27	chr10:90343208-90343258	AG04450	lung:	fetal
28	chr10:90345860-90345910	K562	blood:	n/a
29	chr10:90346597-90346647	HRPEpiC	eye:	n/a
30	chr10:90343166-90343216	HMEC	breast:	n/a
31	chr10:90364671-90364721	HPAEpiC	pulmonary alveolar:	n/a
32	chr10:90346479-90346529	HRCEpiC	kidney:	n/a
33	chr10:90343174-90343224	HUVEC	blood vessel:	n/a
34	chr10:90339186-90339236	HAEpiC	amniotic membrane:	n/a
35	chr10:90341959-90342009	SKMC	muscle:	n/a
36	chr10:90345356-90345406	ECC-1	luminal epithelium:	n/a
37	chr10:90346597-90346647	Hepatocyte	liver:	n/a
38	chr10:90346597-90346647	HMEC	breast:	n/a
39	chr10:90343435-90343485	LNCaP	prostate:	n/a
40	chr10:90342738-90342788	Hepatocyte	liver:	n/a
41	chr10:90343192-90343242	Hela-S3	cervix:	n/a
42	chr10:90346597-90346647	IMR90	lung:	fetal
43	chr10:90343208-90343258	HIPEpiC	eye:	n/a
44	chr10:90343285-90343335	AG10803	skin:	n/a
45	chr10:90343166-90343216	NT2-D1	testis:	n/a
46	chr10:90342814-90342864	K562	blood:	n/a
47	chr10:90346479-90346529	NB4	blood:	n/a
48	chr10:90345170-90345220	HPAEpiC	pulmonary alveolar:	n/a
49	chr10:90343641-90343691	HepG2	liver:	n/a
50	chr10:90346597-90346647	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:89623284..89624802-chr10:90333156..90335627,2	MCF-7	breast:
2	chr10:90341555..90343479-chr10:90350862..90352924,2	MCF-7	breast:
3	chr10:90363656..90365156-chr2:88314680..88316316,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LIPJ-2	chr10:90343084-90344727	NONHSAT015473

Variant related genes	Relation type
ENSG00000201548	TF binding region
LIPJ	TF binding region
RNLS	TF binding region
ENSG00000201548	CpG island
LIPJ	CpG island
RNLS	CpG island
ENSG00000222724	chromatin interactions
ENSG00000171862	chromatin interactions
ENSG00000184719	chromatin interactions

Extended variants
information (count: 991 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:991 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372813574	chr10:90329927-90329928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs149069018	chr10:90329959-90329960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538777730	chr10:90329983-90329984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115029575	chr10:90330010-90330011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187025725	chr10:90330034-90330035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11202774	chr10:90330037-90330038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192480510	chr10:90330050-90330051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs58587048	chr10:90330070-90330071	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs373480628	chr10:90330102-90330103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs57834656	chr10:90330107-90330108	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs181458081	chr10:90330136-90330137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556323757	chr10:90330226-90330227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556662588	chr10:90330253-90330254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577626528	chr10:90330292-90330293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185989787	chr10:90330307-90330308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566491979	chr10:90330353-90330354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2861367	chr10:90330392-90330393	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs1359582	chr10:90330483-90330484	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs190551004	chr10:90330516-90330517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182431612	chr10:90330551-90330552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs79726952	chr10:90330558-90330559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550037722	chr10:90330593-90330594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564990544	chr10:90330624-90330625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561759599	chr10:90330632-90330633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564451036	chr10:90330644-90330645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143016294	chr10:90330705-90330706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555048840	chr10:90330727-90330728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs67169934	chr10:90330728-90330729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs11202775	chr10:90330729-90330730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs199542643	chr10:90330731-90330732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs113107632	chr10:90330732-90330733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs371061891	chr10:90330733-90330734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200710032	chr10:90330740-90330741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201560009	chr10:90330742-90330743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs200036260	chr10:90330745-90330746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200811307	chr10:90330746-90330747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs144516764	chr10:90330747-90330748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560049107	chr10:90330754-90330755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567838621	chr10:90330780-90330781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538014193	chr10:90330850-90330851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556819929	chr10:90330851-90330852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113335351	chr10:90330852-90330853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs60884134	chr10:90330919-90330920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs148186962	chr10:90330939-90330940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs369754141	chr10:90330958-90330959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532375650	chr10:90330959-90330960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs543101879	chr10:90330979-90330980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554506330	chr10:90331030-90331031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76848112	chr10:90331065-90331066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576192503	chr10:90331140-90331141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	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
Melanoma	17363583	CNVD
Prostate cancer	21147910	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
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Melanoma	20877625	CNVD
Ependymoma	20639864	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90312200-90342400	Weak transcription	Ovary	ovary
2	chr10:90315400-90342400	Weak transcription	Aorta	Aorta
3	chr10:90317800-90341800	Weak transcription	Adipose Nuclei	Adipose
4	chr10:90319200-90342000	Weak transcription	Pancreas	Pancrea
5	chr10:90321000-90342000	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr10:90326800-90342400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr10:90330400-90331000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr10:90331000-90332400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr10:90331000-90341800	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr10:90331000-90342400	Weak transcription	Psoas Muscle	Psoas
11	chr10:90331400-90342400	Weak transcription	Left Ventricle	heart
12	chr10:90331600-90331800	Enhancers	Gastric	stomach
13	chr10:90331600-90342400	Weak transcription	Esophagus	oesophagus
14	chr10:90331800-90342000	Weak transcription	Gastric	stomach
15	chr10:90332400-90332600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr10:90336200-90337800	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr10:90337800-90341800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr10:90337800-90341800	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr10:90339600-90342200	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr10:90340400-90341000	Weak transcription	NHDF-Ad	bronchial
21	chr10:90341800-90342000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr10:90341800-90342000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr10:90341800-90342000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr10:90341800-90342000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr10:90341800-90342000	Enhancers	Brain Cingulate Gyrus	brain
26	chr10:90341800-90342000	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr10:90341800-90342000	Enhancers	Small Intestine	intestine
28	chr10:90341800-90342000	Enhancers	Spleen	Spleen
29	chr10:90341800-90342000	Weak transcription	NHDF-Ad	bronchial
30	chr10:90341800-90342200	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr10:90341800-90342200	Enhancers	Adipose Nuclei	Adipose
32	chr10:90341800-90342200	Enhancers	Brain Anterior Caudate	brain
33	chr10:90341800-90342200	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr10:90341800-90342200	Enhancers	Brain Substantia Nigra	brain
35	chr10:90341800-90342200	Enhancers	Colon Smooth Muscle	Colon
36	chr10:90341800-90342200	Enhancers	Osteobl	bone
37	chr10:90341800-90342400	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr10:90341800-90342400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr10:90341800-90342400	Enhancers	Liver	Liver
40	chr10:90341800-90342400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr10:90341800-90343600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr10:90341800-90343800	Active TSS	Skeletal Muscle Female	skeletal muscle
43	chr10:90341800-90343800	Active TSS	Stomach Smooth Muscle	stomach
44	chr10:90342000-90342200	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr10:90342000-90342200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr10:90342000-90342200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr10:90342000-90342200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr10:90342000-90342200	Enhancers	Fetal Brain Female	brain
49	chr10:90342000-90342200	Enhancers	Gastric	stomach
50	chr10:90342000-90342200	Enhancers	NHDF-Ad	bronchial

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