Variant report

Variant	nsv1048399
Chromosome Location	chr10:55151470-55313737
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	chr10:55236413-55237624	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr10:55238974-55239521	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr10:55217223-55217233	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr10:55239117-55239415	H1-hESC	embryonic stem cell:	n/a	chr10:55239353-55239362
5	BCL11A	chr10:55239200-55239377	H1-hESC	embryonic stem cell:	n/a	chr10:55239353-55239362
6	BHLHE40	chr10:55190762-55191068	GM12878	blood:	n/a	n/a
7	BHLHE40	chr10:55191987-55192023	GM12878	blood:	n/a	n/a
8	BRCA1	chr10:55236620-55237424	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr10:55239096-55239406	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr10:55163410-55163758	MCF-7	breast:	n/a	n/a
11	CEBPB	chr10:55152197-55152412	IMR90	lung:	n/a	chr10:55152322-55152331 chr10:55152322-55152331 chr10:55152322-55152331 chr10:55152225-55152236 chr10:55152362-55152373 chr10:55152225-55152238 chr10:55152225-55152238 chr10:55152225-55152236 chr10:55152322-55152331 chr10:55152320-55152331
12	CEBPB	chr10:55152219-55152475	HepG2	liver:	n/a	chr10:55152322-55152331 chr10:55152322-55152331 chr10:55152322-55152331 chr10:55152225-55152236 chr10:55152362-55152373 chr10:55152225-55152238 chr10:55152225-55152238 chr10:55152225-55152236 chr10:55152322-55152331 chr10:55152320-55152331
13	CEBPB	chr10:55250388-55250668	H1-hESC	embryonic stem cell:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
14	CEBPB	chr10:55250331-55250691	HepG2	liver:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
15	CEBPB	chr10:55312611-55312881	IMR90	lung:	n/a	chr10:55312751-55312762 chr10:55312749-55312766
16	CEBPB	chr10:55239054-55239539	H1-hESC	embryonic stem cell:	n/a	chr10:55239464-55239475 chr10:55239371-55239383
17	CEBPB	chr10:55250334-55250666	K562	blood:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
18	CEBPB	chr10:55250389-55250679	Hela-S3	cervix:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
19	CEBPB	chr10:55233744-55234036	HepG2	liver:	n/a	chr10:55233869-55233880
20	CEBPB	chr10:55312702-55312890	A549	lung:	n/a	chr10:55312751-55312762 chr10:55312749-55312766
21	CEBPB	chr10:55312604-55312917	HepG2	liver:	n/a	chr10:55312751-55312762 chr10:55312749-55312766
22	CEBPB	chr10:55312660-55312904	H1-hESC	embryonic stem cell:	n/a	chr10:55312751-55312762 chr10:55312749-55312766
23	CEBPB	chr10:55188572-55188772	HepG2	liver:	n/a	n/a
24	CEBPB	chr10:55250346-55250673	IMR90	lung:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
25	CEBPB	chr10:55311076-55311349	HepG2	liver:	n/a	chr10:55311194-55311205
26	CEBPB	chr10:55294104-55294156	A549	lung:	n/a	n/a
27	CEBPB	chr10:55250360-55250591	A549	lung:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
28	CHD1	chr10:55269600-55269603	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr10:55239006-55239395	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr10:55236611-55237504	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr10:55238997-55239826	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr10:55164440-55164590	Caco-2	colon:	n/a	n/a
33	CTCF	chr10:55294120-55294270	MCF-7	breast:	n/a	n/a
34	CTCF	chr10:55213060-55213210	HEK293	kidney:	n/a	chr10:55213102-55213110
35	CTCF	chr10:55213120-55213270	NB4	blood:	n/a	n/a
36	CTCF	chr10:55213120-55213270	NHEK	skin:	n/a	n/a
37	CTCF	chr10:55213075-55213175	LNCaP	prostate:	n/a	chr10:55213102-55213110
38	CTCF	chr10:55213093-55213177	SK-N-SH_RA	brain:	n/a	chr10:55213102-55213110
39	CTCF	chr10:55213049-55213215	SK-N-SH_RA	brain:	n/a	chr10:55213102-55213110
40	CTCF	chr10:55182320-55182470	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr10:55213040-55213190	SAEC	small airway:	n/a	chr10:55213102-55213110
42	CTCF	chr10:55182380-55182530	HEK293	kidney:	n/a	n/a
43	CTCF	chr10:55213063-55213254	HUVEC	blood vessel:	n/a	chr10:55213102-55213110
44	CTCF	chr10:55213097-55213196	GM10266	blood:	n/a	chr10:55213102-55213110
45	CTCF	chr10:55213100-55213250	HEK293	kidney:	n/a	chr10:55213102-55213110
46	CTCF	chr10:55213060-55213210	HPF	lung:	n/a	chr10:55213102-55213110
47	CTCF	chr10:55213060-55213210	HA-sp	spinal cord:	n/a	chr10:55213102-55213110
48	CTCF	chr10:55213120-55213270	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr10:55213060-55213210	HRE	kidney:	n/a	chr10:55213102-55213110
50	CTCF	chr10:55213060-55213210	HRPEpiC	eye:	n/a	chr10:55213102-55213110

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:55259527-55259577	HPAEpiC	pulmonary alveolar:	n/a
2	chr10:55259527-55259577	SAEC	small airway:	n/a
3	chr10:55259527-55259577	HepG2	liver:	n/a
4	chr10:55259527-55259577	ovcar-3	ovarian:	n/a
5	chr10:55259527-55259577	BJ	skin:	n/a
6	chr10:55259527-55259577	ECC-1	luminal epithelium:	n/a
7	chr10:55259527-55259577	HCM	heart:	n/a
8	chr10:55259527-55259577	SK-N-SH	brain:	n/a
9	chr10:55259527-55259577	H1-hESC	embryonic stem cell:	embryo
10	chr10:55259527-55259577	HCF	heart:	n/a
11	chr10:55259527-55259577	IMR90	lung:	fetal
12	chr10:55259527-55259577	A549	lung:	n/a
13	chr10:55259527-55259577	BE2_C	brain:	n/a
14	chr10:55259527-55259577	HNPCEpiC	eye:	n/a
15	chr10:55259527-55259577	HAEpiC	amniotic membrane:	n/a
16	chr10:55259527-55259577	PrEC	prostate:	n/a
17	chr10:55259527-55259577	NB4	blood:	n/a
18	chr10:55259527-55259577	RPTEC	kidney:	n/a
19	chr10:55259527-55259577	T-47D	breast:	n/a
20	chr10:55259527-55259577	SK-N-SH_RA	brain:	n/a
21	chr10:55259527-55259577	NT2-D1	testis:	n/a
22	chr10:55259527-55259577	ProgFib	skin:	n/a
23	chr10:55259527-55259577	HEEpiC	esophagus:	n/a
24	chr10:55259527-55259577	GM12878	blood:	n/a
25	chr10:55259527-55259577	GM06990	blood:	n/a
26	chr10:55259527-55259577	AoSMC	blood vessel:	n/a
27	chr10:55259527-55259577	Jurkat	blood:	n/a
28	chr10:55259527-55259577	GM12891	blood:	n/a
29	chr10:55259527-55259577	HIPEpiC	eye:	n/a
30	chr10:55259527-55259577	NH-A	brain:	n/a
31	chr10:55259527-55259577	AG04449	skin:	fetal
32	chr10:55259527-55259577	Caco-2	colon:	n/a
33	chr10:55259527-55259577	Hela-S3	cervix:	n/a
34	chr10:55259527-55259577	HL-60	blood:	n/a
35	chr10:55259527-55259577	HRPEpiC	eye:	n/a
36	chr10:55259527-55259577	HRCEpiC	kidney:	n/a
37	chr10:55259527-55259577	HMEC	breast:	n/a
38	chr10:55259527-55259577	PANC-1	pancreas:	n/a
39	chr10:55259527-55259577	AG09319	gingival:	n/a
40	chr10:55259527-55259577	SK-N-MC	brain:	n/a
41	chr10:55259527-55259577	GM12892	blood:	n/a
42	chr10:55259527-55259577	AG09309	skin:	n/a
43	chr10:55259527-55259577	CMK	blood:	n/a
44	chr10:55259527-55259577	NHDF-neo	bronchial:	n/a
45	chr10:55259527-55259577	SKMC	muscle:	n/a
46	chr10:55259527-55259577	MCF-7	breast:	n/a
47	chr10:55259527-55259577	K562	blood:	n/a
48	chr10:55259527-55259577	HEK293	kidney:	embryo
49	chr10:55259527-55259577	MCF10A-Er-Src	breast:	n/a
50	chr10:55259527-55259577	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:55313361..55315052-chr10:55318156..55320737,2	K562	blood:
2	chr10:55298474..55301304-chr10:55304357..55306392,2	MCF-7	breast:
3	chr10:55303514..55305516-chr10:55305569..55307810,2	K562	blood:
4	chr10:55171490..55173538-chr10:55175367..55178317,2	K562	blood:
5	chr10:55278002..55279503-chr7:30548599..30550148,2	MCF-7	breast:
6	chr10:55303514..55305516-chr10:55305569..55307810,2	K562	blood:
7	chr10:55171490..55173538-chr10:55175367..55178317,2	K562	blood:
8	chr10:55228435..55230987-chr10:55235490..55236993,2	K562	blood:
9	chr10:55271750..55273969-chr10:55282270..55285131,2	MCF-7	breast:
10	chr10:55271750..55273969-chr10:55282270..55285131,2	MCF-7	breast:
11	chr10:55298474..55301304-chr10:55304357..55306392,2	MCF-7	breast:
12	chr10:55228435..55230987-chr10:55235490..55236993,2	K562	blood:

Variant related genes	Relation type
RNA5SP318	TF binding region
RNA5SP318	CpG island

Extended variants
information (count: 6301 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:6301 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145713544	chr10:55151476-55151477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs371982337	chr10:55151482-55151483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181313995	chr10:55151484-55151485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574980751	chr10:55151486-55151487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs151050330	chr10:55151502-55151503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560855307	chr10:55151505-55151506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184307938	chr10:55151560-55151561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189113425	chr10:55151561-55151562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562178735	chr10:55151602-55151603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs5784998	chr10:55151646-55151647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs398075161	chr10:55151647-55151648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs398013475	chr10:55151648-55151649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576990523	chr10:55151708-55151709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs116153532	chr10:55151754-55151755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375494569	chr10:55151755-55151756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541570641	chr10:55151834-55151835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561682627	chr10:55151838-55151839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs16937424	chr10:55151886-55151887	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs547336904	chr10:55151894-55151895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570743922	chr10:55151924-55151925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs116649211	chr10:55151960-55151961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375023344	chr10:55151966-55151967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552598110	chr10:55152003-55152004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs16937426	chr10:55152071-55152072	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs538295748	chr10:55152146-55152147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140835526	chr10:55152184-55152185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181726010	chr10:55152189-55152190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187419072	chr10:55152259-55152260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534427580	chr10:55152279-55152280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375961097	chr10:55152284-55152285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554099550	chr10:55152290-55152291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551675169	chr10:55152305-55152306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571499002	chr10:55152348-55152349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577450014	chr10:55152364-55152365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35517251	chr10:55152367-55152368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549922682	chr10:55152382-55152383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546127184	chr10:55152391-55152392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555735929	chr10:55152406-55152407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150151584	chr10:55152410-55152411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371953494	chr10:55152474-55152475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528495497	chr10:55152475-55152476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541482111	chr10:55152483-55152484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561834552	chr10:55152497-55152498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527465173	chr10:55152563-55152564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7476064	chr10:55152565-55152566	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs10762976	chr10:55152617-55152618	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs10825014	chr10:55152664-55152665	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs550105536	chr10:55152704-55152705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569236029	chr10:55152710-55152711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374363838	chr10:55152737-55152738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Dysmorphic features	21948486	CNVD
Epilepsy	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	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

Chromatin state (count:454 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55149800-55154200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr10:55151200-55155400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr10:55152600-55153600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr10:55153400-55154800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
5	chr10:55153400-55157000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr10:55153800-55156800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr10:55154200-55156400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
8	chr10:55154400-55157600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
9	chr10:55154600-55155800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr10:55154800-55156400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
11	chr10:55155400-55155800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr10:55155600-55156200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
13	chr10:55155800-55157400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr10:55156800-55157600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
15	chr10:55161200-55162600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr10:55161400-55161600	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
17	chr10:55161600-55162600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr10:55162200-55165600	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr10:55162200-55166400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr10:55162600-55163000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr10:55162600-55164600	Enhancers	Fetal Muscle Leg	muscle
22	chr10:55162800-55163600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr10:55162800-55164400	Enhancers	Liver	Liver
24	chr10:55162800-55164800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr10:55163000-55164200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr10:55163000-55164600	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr10:55163000-55164800	Enhancers	Fetal Heart	heart
28	chr10:55163000-55164800	Enhancers	Fetal Muscle Trunk	muscle
29	chr10:55163000-55164800	Enhancers	HUVEC	blood vessel
30	chr10:55163200-55163400	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr10:55163200-55164200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr10:55163200-55164200	Enhancers	Left Ventricle	heart
33	chr10:55163200-55165200	Enhancers	Fetal Brain Male	brain
34	chr10:55163200-55165200	Enhancers	Fetal Brain Female	brain
35	chr10:55163400-55164200	Enhancers	Adipose Nuclei	Adipose
36	chr10:55163400-55164200	Enhancers	Ovary	ovary
37	chr10:55163400-55164200	Enhancers	Pancreas	Pancrea
38	chr10:55163400-55164200	Enhancers	Right Atrium	heart
39	chr10:55163400-55164200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
40	chr10:55163400-55164400	Enhancers	Brain Germinal Matrix	brain
41	chr10:55163400-55164400	Enhancers	Stomach Mucosa	stomach
42	chr10:55163400-55164600	Enhancers	Gastric	stomach
43	chr10:55163400-55164600	Enhancers	Lung	lung
44	chr10:55163400-55164600	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr10:55163400-55164600	Enhancers	Spleen	Spleen
46	chr10:55163600-55164000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr10:55163600-55164200	Enhancers	Primary hematopoietic stem cells	blood
48	chr10:55163600-55164400	Enhancers	Fetal Stomach	stomach
49	chr10:55164000-55165000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr10:55164200-55164400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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