Variant report

Variant	nsv895410
Chromosome Location	chr10:55385962-55577022
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	chr10:55546113-55546324	HepG2	liver:	n/a	n/a
2	BACH1	chr10:55410674-55410823	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr10:55436651-55436653	Hela-S3	cervix:	n/a	n/a
4	CCNT2	chr10:55407553-55407753	K562	blood:	n/a	n/a
5	CEBPB	chr10:55482323-55482573	IMR90	lung:	n/a	chr10:55482450-55482463 chr10:55482451-55482462 chr10:55482452-55482461 chr10:55482452-55482461 chr10:55482450-55482461 chr10:55482452-55482461 chr10:55482450-55482463 chr10:55482452-55482461 chr10:55482450-55482463
6	CEBPB	chr10:55484473-55484797	IMR90	lung:	n/a	chr10:55484642-55484651 chr10:55484640-55484651 chr10:55484642-55484653 chr10:55484640-55484653
7	CEBPB	chr10:55572413-55572622	H1-hESC	embryonic stem cell:	n/a	chr10:55572521-55572530 chr10:55572521-55572530 chr10:55572519-55572532 chr10:55572521-55572530
8	CEBPB	chr10:55411770-55412027	HepG2	liver:	n/a	chr10:55411925-55411936
9	CEBPB	chr10:55495022-55495339	HepG2	liver:	n/a	n/a
10	CEBPB	chr10:55440212-55440489	A549	lung:	n/a	chr10:55440348-55440359
11	CEBPB	chr10:55572397-55572600	HepG2	liver:	n/a	chr10:55572521-55572530 chr10:55572521-55572530 chr10:55572519-55572532 chr10:55572521-55572530
12	CEBPB	chr10:55484474-55484818	HepG2	liver:	n/a	chr10:55484642-55484651 chr10:55484640-55484651 chr10:55484642-55484653 chr10:55484640-55484653
13	CEBPB	chr10:55440562-55440588	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr10:55495107-55495314	A549	lung:	n/a	n/a
15	CEBPB	chr10:55495099-55495137	K562	blood:	n/a	n/a
16	CEBPB	chr10:55482351-55482593	HepG2	liver:	n/a	chr10:55482450-55482463 chr10:55482451-55482462 chr10:55482452-55482461 chr10:55482452-55482461 chr10:55482450-55482461 chr10:55482452-55482461 chr10:55482450-55482463 chr10:55482452-55482461 chr10:55482450-55482463
17	CEBPB	chr10:55440189-55440480	HepG2	liver:	n/a	chr10:55440348-55440359
18	CEBPB	chr10:55456808-55457116	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr10:55440217-55440437	IMR90	lung:	n/a	chr10:55440348-55440359
20	CEBPB	chr10:55531808-55532061	HepG2	liver:	n/a	chr10:55531918-55531929
21	CEBPB	chr10:55531788-55532061	IMR90	lung:	n/a	chr10:55531918-55531929
22	CEBPB	chr10:55573444-55573642	HepG2	liver:	n/a	chr10:55573508-55573519
23	CEBPB	chr10:55539511-55539751	HepG2	liver:	n/a	n/a
24	CEBPB	chr10:55494993-55495303	IMR90	lung:	n/a	n/a
25	CEBPB	chr10:55407097-55407340	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr10:55484526-55484810	A549	lung:	n/a	chr10:55484642-55484651 chr10:55484640-55484651 chr10:55484642-55484653 chr10:55484640-55484653
27	CEBPB	chr10:55411759-55412117	Hela-S3	cervix:	n/a	chr10:55411925-55411936
28	CEBPB	chr10:55531778-55532075	H1-hESC	embryonic stem cell:	n/a	chr10:55531918-55531929
29	CHD1	chr10:55509966-55509970	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr10:55546058-55546349	K562	blood:	n/a	n/a
31	CTCF	chr10:55568567-55568709	MCF-7	breast:	n/a	n/a
32	CTCF	chr10:55546140-55546290	K562	blood:	n/a	n/a
33	CTCF	chr10:55546174-55546229	GM10248	blood:	n/a	n/a
34	CTCF	chr10:55568586-55568720	LNCaP	prostate:	n/a	n/a
35	CTCF	chr10:55568460-55568610	HMEC	breast:	n/a	n/a
36	CTCF	chr10:55568544-55568762	Gliobla	brain:	n/a	n/a
37	CTCF	chr10:55568540-55568690	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr10:55546080-55546230	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr10:55546103-55546323	GM13977	blood:	n/a	n/a
40	CTCF	chr10:55546078-55546280	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr10:55546182-55546212	MCF-7	breast:	n/a	n/a
42	CTCF	chr10:55568484-55568802	T-47D	breast:	n/a	n/a
43	CTCF	chr10:55546140-55546290	HepG2	liver:	n/a	n/a
44	CTCF	chr10:55546139-55546250	LNCaP	prostate:	n/a	n/a
45	CTCF	chr10:55546020-55546170	HMEC	breast:	n/a	n/a
46	CTCF	chr10:55572247-55572258	GM20000	blood:	n/a	n/a
47	CTCF	chr10:55546080-55546230	GM12875	blood:	n/a	n/a
48	CTCF	chr10:55546087-55546313	Medullo	brain:	n/a	n/a
49	CTCF	chr10:55546060-55546210	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr10:55568540-55568690	BE2_C	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:55393450-55393500	ECC-1	luminal epithelium:	n/a
2	chr10:55393450-55393500	CMK	blood:	n/a
3	chr10:55419714-55419764	BE2_C	brain:	n/a
4	chr10:55568997-55569047	NHDF-neo	bronchial:	n/a
5	chr10:55393450-55393500	T-47D	breast:	n/a
6	chr10:55419927-55419977	GM19239	blood:	n/a
7	chr10:55419927-55419977	LNCaP	prostate:	n/a
8	chr10:55393450-55393500	Caco-2	colon:	n/a
9	chr10:55419927-55419977	AG09319	gingival:	n/a
10	chr10:55419927-55419977	SK-N-SH	brain:	n/a
11	chr10:55419714-55419764	HCPEpiC	choroid plexus:	n/a
12	chr10:55568997-55569047	HCM	heart:	n/a
13	chr10:55419714-55419764	AG10803	skin:	n/a
14	chr10:55393450-55393500	HRCEpiC	kidney:	n/a
15	chr10:55419714-55419764	HUVEC	blood vessel:	n/a
16	chr10:55419714-55419764	MCF10A-Er-Src	breast:	n/a
17	chr10:55419714-55419764	Jurkat	blood:	n/a
18	chr10:55419927-55419977	ovcar-3	ovarian:	n/a
19	chr10:55419714-55419764	AoSMC	blood vessel:	n/a
20	chr10:55419927-55419977	BJ	skin:	n/a
21	chr10:55568997-55569047	SKMC	muscle:	n/a
22	chr10:55568997-55569047	MCF10A-Er-Src	breast:	n/a
23	chr10:55568997-55569047	SK-N-MC	brain:	n/a
24	chr10:55568997-55569047	NB4	blood:	n/a
25	chr10:55419927-55419977	NHBE	bronchial:	n/a
26	chr10:55568997-55569047	SK-N-SH	brain:	n/a
27	chr10:55393450-55393500	SK-N-SH_RA	brain:	n/a
28	chr10:55419714-55419764	CMK	blood:	n/a
29	chr10:55419714-55419764	NB4	blood:	n/a
30	chr10:55568997-55569047	IMR90	lung:	fetal
31	chr10:55568997-55569047	GM12878	blood:	n/a
32	chr10:55419714-55419764	ECC-1	luminal epithelium:	n/a
33	chr10:55419927-55419977	U87	brain:	n/a
34	chr10:55393450-55393500	GM19239	blood:	n/a
35	chr10:55393450-55393500	HCT-116	colon:	n/a
36	chr10:55419714-55419764	HEK293	kidney:	embryo
37	chr10:55419927-55419977	SK-N-SH_RA	brain:	n/a
38	chr10:55419714-55419764	RPTEC	kidney:	n/a
39	chr10:55568997-55569047	BJ	skin:	n/a
40	chr10:55568997-55569047	HL-60	blood:	n/a
41	chr10:55568997-55569047	HCPEpiC	choroid plexus:	n/a
42	chr10:55568997-55569047	SK-N-SH_RA	brain:	n/a
43	chr10:55419927-55419977	PFSK-1	brain:	n/a
44	chr10:55568997-55569047	HEK293	kidney:	embryo
45	chr10:55419927-55419977	NHDF-neo	bronchial:	n/a
46	chr10:55419714-55419764	HCM	heart:	n/a
47	chr10:55568997-55569047	HCF	heart:	n/a
48	chr10:55419927-55419977	GM06990	blood:	n/a
49	chr10:55568997-55569047	HCT-116	colon:	n/a
50	chr10:55419927-55419977	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:55466040..55468835-chr10:55471879..55474110,2	K562	blood:
2	chr10:55405153..55407581-chr5:63345532..63348450,2	MCF-7	breast:
3	chr10:55481740..55482260-chr20:52673713..52674214,2	MCF-7	breast:
4	chr10:55057963..55058535-chr10:55568196..55569129,2	MCF-7	breast:
5	chr10:55549906..55552050-chr10:55558959..55560597,2	K562	blood:
6	chr10:55466040..55468835-chr10:55471879..55474110,2	K562	blood:
7	chr10:55558585..55559152-chr17:58469714..58470538,2	MCF-7	breast:
8	10:55527193-55535408..10:55949104-55956834	K562	blood:
9	chr10:55549906..55552050-chr10:55558959..55560597,2	K562	blood:
10	chr10:55360883..55361625-chr10:55568215..55569121,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DKK1-4	chr10:55526160-55526374	NONHSAT013453

Variant related genes	Relation type
ENSG00000233805	TF binding region
ENSG00000233805	CpG island
ENSG00000170832	chromatin interactions
ENSG00000141371	chromatin interactions

Extended variants
information (count: 3138 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:3138 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7095328	chr10:55385962-55385963	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185290557	chr10:55385964-55385965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367785633	chr10:55385983-55385984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540991926	chr10:55386049-55386050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1489836	chr10:55386129-55386130	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs533037601	chr10:55386141-55386142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543538689	chr10:55386265-55386266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563328639	chr10:55386297-55386298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199830119	chr10:55386307-55386308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200213684	chr10:55386313-55386314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs397767888	chr10:55386316-55386317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs5785008	chr10:55386317-55386318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200069402	chr10:55386318-55386319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529133442	chr10:55386344-55386345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139414268	chr10:55386370-55386371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188737117	chr10:55386540-55386541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs73235876	chr10:55386557-55386558	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs547360675	chr10:55386592-55386593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs1387655	chr10:55386595-55386596	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs368492053	chr10:55386614-55386615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369476231	chr10:55386627-55386628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371914506	chr10:55386629-55386630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527454454	chr10:55386644-55386645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs57244760	chr10:55386646-55386647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111893642	chr10:55386655-55386656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10825077	chr10:55386673-55386674	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs376542069	chr10:55386816-55386817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149628042	chr10:55386914-55386915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536089063	chr10:55386946-55386947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555668358	chr10:55386965-55386966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572805583	chr10:55386971-55386972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144245147	chr10:55386978-55386979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181703751	chr10:55386988-55386989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187122407	chr10:55387046-55387047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191895873	chr10:55387111-55387112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563443480	chr10:55387118-55387119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573644388	chr10:55387168-55387169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372615095	chr10:55387196-55387197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148708057	chr10:55387251-55387252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183941441	chr10:55387262-55387263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112926109	chr10:55387264-55387265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551224079	chr10:55387269-55387270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73235879	chr10:55387381-55387382	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs78103184	chr10:55387384-55387385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs74482215	chr10:55387437-55387438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570168657	chr10:55387454-55387455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370814270	chr10:55387473-55387474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559630230	chr10:55387478-55387479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146831086	chr10:55387545-55387546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139612246	chr10:55387547-55387548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
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
Thoracic aortic aneurysm	21092924	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
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	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
Obesity	21956041	CNVD
Developmental delay	21948486	CNVD
Intellectual disability	21948486	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Colorectal cancer	16774939	CNVD
Autism	20858243	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD
Usher type I cohort	17277737	CNVD
Usher type I cohort	21436283	CNVD
Leukemia	21357790	CNVD
Medulloblastoma	22832581	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55379800-55387600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr10:55390400-55390600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr10:55390600-55394000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr10:55394000-55394400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr10:55394200-55394400	Enhancers	Fetal Kidney	kidney
6	chr10:55394200-55395200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr10:55394400-55395200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:55395000-55395200	Enhancers	Fetal Kidney	kidney
9	chr10:55397000-55398400	Enhancers	Fetal Lung	lung
10	chr10:55397800-55398400	Enhancers	Primary hematopoietic stem cells	blood
11	chr10:55398400-55403200	Weak transcription	Fetal Lung	lung
12	chr10:55403200-55406200	Enhancers	Fetal Lung	lung
13	chr10:55405200-55407400	Enhancers	Fetal Stomach	stomach
14	chr10:55406200-55406600	Flanking Active TSS	Fetal Lung	lung
15	chr10:55406200-55406600	Enhancers	Stomach Smooth Muscle	stomach
16	chr10:55406400-55407200	Enhancers	Fetal Brain Male	brain
17	chr10:55406600-55409000	Enhancers	Fetal Lung	lung
18	chr10:55407400-55408400	Weak transcription	Fetal Stomach	stomach
19	chr10:55408600-55408800	Enhancers	Fetal Stomach	stomach
20	chr10:55417600-55418400	Enhancers	Fetal Heart	heart
21	chr10:55418400-55424200	Weak transcription	Fetal Heart	heart
22	chr10:55422400-55423000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr10:55422400-55424400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr10:55422400-55424400	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr10:55423000-55423400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr10:55423400-55426600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr10:55423600-55424200	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr10:55423800-55424200	Enhancers	Fetal Lung	lung
29	chr10:55424000-55424200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr10:55424000-55424400	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr10:55424000-55425000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr10:55424000-55425000	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr10:55424200-55424400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr10:55424200-55424400	Active TSS	Adipose Nuclei	Adipose
35	chr10:55424200-55424600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr10:55424200-55424600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
37	chr10:55424200-55424600	Active TSS	Fetal Kidney	kidney
38	chr10:55424200-55424600	Active TSS	Stomach Smooth Muscle	stomach
39	chr10:55424200-55424800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr10:55424200-55424800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
41	chr10:55424200-55424800	Flanking Active TSS	Fetal Lung	lung
42	chr10:55424200-55424800	Active TSS	Rectal Mucosa Donor 29	rectum
43	chr10:55424200-55425000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr10:55424200-55425000	Enhancers	Fetal Heart	heart
45	chr10:55424200-55425000	Enhancers	Fetal Intestine Small	intestine
46	chr10:55424200-55425000	Enhancers	Fetal Stomach	stomach
47	chr10:55424400-55424600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr10:55424400-55424800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr10:55424400-55424800	Flanking Active TSS	Adipose Nuclei	Adipose
50	chr10:55424400-55424800	Enhancers	Liver	Liver

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