Variant report

Variant	nsv465628
Chromosome Location	chr1:171381746-171409515
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	ATF1	chr1:171392674-171392783	K562	blood:	n/a	n/a
2	ATF1	chr1:171405080-171405221	K562	blood:	n/a	n/a
3	BCL11A	chr1:171401209-171401460	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr1:171401181-171401466	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr1:171407411-171408095	HCT-116	colon:	n/a	n/a
6	CBX3	chr1:171407198-171408114	HCT-116	colon:	n/a	n/a
7	CEBPB	chr1:171403737-171404352	A549	lung:	n/a	n/a
8	CEBPB	chr1:171403840-171404290	IMR90	lung:	n/a	n/a
9	CEBPB	chr1:171403845-171404207	A549	lung:	n/a	n/a
10	CEBPB	chr1:171403820-171404596	Hela-S3	cervix:	n/a	n/a
11	CHD2	chr1:171403861-171404345	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr1:171407622-171407928	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr1:171400962-171401546	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTBP2	chr1:171400266-171401076	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr1:171399213-171399268	GM20000	blood:	n/a	n/a
16	CTCF	chr1:171403566-171403591	GM10266	blood:	n/a	n/a
17	CTCF	chr1:171388922-171388991	Kidney_OC	kidney:	n/a	n/a
18	E2F4	chr1:171403989-171404193	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr1:171390072-171390536	MCF10A-Er-Src	breast:	n/a	chr1:171390464-171390481
20	E2F4	chr1:171407485-171408000	MCF10A-Er-Src	breast:	n/a	n/a
21	ELK1	chr1:171390082-171390227	GM12878	blood:	n/a	n/a
22	ELK4	chr1:171403929-171404690	Hela-S3	cervix:	n/a	n/a
23	ELK4	chr1:171407552-171408083	Hela-S3	cervix:	n/a	n/a
24	EP300	chr1:171401065-171401523	H1-hESC	embryonic stem cell:	n/a	n/a
25	EP300	chr1:171407617-171407911	SK-N-SH_RA	brain:	n/a	n/a
26	EP300	chr1:171407399-171408253	SK-N-SH	brain:	n/a	n/a
27	EP300	chr1:171407547-171408176	Hela-S3	cervix:	n/a	n/a
28	EP300	chr1:171403932-171404267	SK-N-SH_RA	brain:	n/a	n/a
29	EP300	chr1:171401098-171401464	H1-hESC	embryonic stem cell:	n/a	n/a
30	EP300	chr1:171403932-171404386	SK-N-SH_RA	brain:	n/a	chr1:171404283-171404297 chr1:171404287-171404296
31	EP300	chr1:171407591-171407910	SK-N-SH_RA	brain:	n/a	n/a
32	EP300	chr1:171403893-171404536	Hela-S3	cervix:	n/a	chr1:171404283-171404297 chr1:171404287-171404296
33	FOS	chr1:171389921-171390555	MCF10A-Er-Src	breast:	n/a	chr1:171390098-171390107 chr1:171390098-171390108 chr1:171390098-171390108 chr1:171390098-171390108 chr1:171390036-171390045 chr1:171390098-171390108
34	FOS	chr1:171393747-171393773	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr1:171402635-171403530	MCF10A-Er-Src	breast:	n/a	chr1:171403139-171403151 chr1:171402690-171402698
36	FOS	chr1:171389925-171390422	MCF10A-Er-Src	breast:	n/a	chr1:171390098-171390107 chr1:171390098-171390108 chr1:171390098-171390108 chr1:171390098-171390108 chr1:171390036-171390045 chr1:171390098-171390108
37	FOS	chr1:171389922-171390407	MCF10A-Er-Src	breast:	n/a	chr1:171390098-171390107 chr1:171390098-171390108 chr1:171390098-171390108 chr1:171390098-171390108 chr1:171390036-171390045 chr1:171390098-171390108
38	FOS	chr1:171402652-171402990	MCF10A-Er-Src	breast:	n/a	chr1:171402690-171402698
39	FOS	chr1:171403858-171404725	MCF10A-Er-Src	breast:	n/a	chr1:171404110-171404119 chr1:171404108-171404119
40	FOS	chr1:171389893-171390539	MCF10A-Er-Src	breast:	n/a	chr1:171390098-171390107 chr1:171390098-171390108 chr1:171390098-171390108 chr1:171390098-171390108 chr1:171390036-171390045 chr1:171390098-171390108
41	FOS	chr1:171403844-171404715	MCF10A-Er-Src	breast:	n/a	chr1:171404110-171404119 chr1:171404108-171404119
42	FOS	chr1:171402628-171403532	MCF10A-Er-Src	breast:	n/a	chr1:171403139-171403151 chr1:171402690-171402698
43	FOS	chr1:171403871-171404716	MCF10A-Er-Src	breast:	n/a	chr1:171404110-171404119 chr1:171404108-171404119
44	FOS	chr1:171393714-171393940	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr1:171407467-171408226	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr1:171403838-171404707	HUVEC	blood vessel:	n/a	chr1:171404110-171404119 chr1:171404108-171404119
47	FOS	chr1:171402646-171402988	MCF10A-Er-Src	breast:	n/a	chr1:171402690-171402698
48	FOS	chr1:171407524-171408128	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr1:171407535-171408138	HUVEC	blood vessel:	n/a	n/a
50	FOS	chr1:171393699-171393886	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:171407789-171407839	GM12892	blood:	n/a
2	chr1:171407789-171407839	GM12892	blood:	n/a
3	chr1:171399407-171399457	HUVEC	blood vessel:	n/a
4	chr1:171407789-171407839	GM19239	blood:	n/a
5	chr1:171399407-171399457	SK-N-SH_RA	brain:	n/a
6	chr1:171399407-171399457	A549	lung:	n/a
7	chr1:171407789-171407839	SAEC	small airway:	n/a
8	chr1:171407789-171407839	SKMC	muscle:	n/a
9	chr1:171407789-171407839	HAEpiC	amniotic membrane:	n/a
10	chr1:171407789-171407839	HMEC	breast:	n/a
11	chr1:171399407-171399457	AG09309	skin:	n/a
12	chr1:171399407-171399457	HCF	heart:	n/a
13	chr1:171407789-171407839	RPTEC	kidney:	n/a
14	chr1:171407789-171407839	AG04449	skin:	fetal
15	chr1:171407789-171407839	AG10803	skin:	n/a
16	chr1:171399407-171399457	AG10803	skin:	n/a
17	chr1:171399407-171399457	RPTEC	kidney:	n/a
18	chr1:171407789-171407839	NHDF-neo	bronchial:	n/a
19	chr1:171407789-171407839	PANC-1	pancreas:	n/a
20	chr1:171407789-171407839	NT2-D1	testis:	n/a
21	chr1:171407789-171407839	CMK	blood:	n/a
22	chr1:171407789-171407839	HRE	kidney:	n/a
23	chr1:171407789-171407839	HUVEC	blood vessel:	n/a
24	chr1:171399407-171399457	HRE	kidney:	n/a
25	chr1:171399407-171399457	HCPEpiC	choroid plexus:	n/a
26	chr1:171399407-171399457	AG09319	gingival:	n/a
27	chr1:171407789-171407839	A549	lung:	n/a
28	chr1:171407789-171407839	HNPCEpiC	eye:	n/a
29	chr1:171399407-171399457	GM06990	blood:	n/a
30	chr1:171407789-171407839	HCPEpiC	choroid plexus:	n/a
31	chr1:171399407-171399457	PANC-1	pancreas:	n/a
32	chr1:171399407-171399457	HAEpiC	amniotic membrane:	n/a
33	chr1:171407789-171407839	MCF-7	breast:	n/a
34	chr1:171399407-171399457	U87	brain:	n/a
35	chr1:171407789-171407839	MCF10A-Er-Src	breast:	n/a
36	chr1:171407789-171407839	AG09319	gingival:	n/a
37	chr1:171399407-171399457	BJ	skin:	n/a
38	chr1:171399407-171399457	IMR90	lung:	fetal
39	chr1:171399407-171399457	MCF10A-Er-Src	breast:	n/a
40	chr1:171399407-171399457	Hela-S3	cervix:	n/a
41	chr1:171399407-171399457	HCT-116	colon:	n/a
42	chr1:171407789-171407839	ECC-1	luminal epithelium:	n/a
43	chr1:171399407-171399457	HepG2	liver:	n/a
44	chr1:171399407-171399457	AG04450	lung:	fetal
45	chr1:171399407-171399457	ProgFib	skin:	n/a
46	chr1:171399407-171399457	HEK293	kidney:	embryo
47	chr1:171407789-171407839	HPAEpiC	pulmonary alveolar:	n/a
48	chr1:171407789-171407839	NHBE	bronchial:	n/a
49	chr1:171399407-171399457	Caco-2	colon:	n/a
50	chr1:171407789-171407839	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:171387474..171389314-chr1:171452671..171455451,2	MCF-7	breast:
2	chr1:171405355..171408089-chr1:171454758..171456497,2	MCF-7	breast:
3	chr1:171404013..171405651-chr1:171411065..171412627,2	K562	blood:
4	chr1:171368098..171369611-chr1:171388402..171390157,2	MCF-7	breast:
5	chr1:171392802..171395770-chr1:171453289..171456118,2	MCF-7	breast:

Variant related genes	Relation type
RNU6-290P	TF binding region
RNU6-290P	CpG island
ENSG00000117523	chromatin interactions

Extended variants
information (count: 1169 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1169 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560642153	chr1:171383004-171383005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs527399198	chr1:171383039-171383040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs12145071	chr1:171383109-171383110	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs567275982	chr1:171383136-171383137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537896861	chr1:171383161-171383162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs549499975	chr1:171383162-171383163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571549373	chr1:171383183-171383184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538532346	chr1:171383197-171383198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374716255	chr1:171383198-171383199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs571873362	chr1:171383203-171383204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534036742	chr1:171383214-171383215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555394975	chr1:171383215-171383216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186367596	chr1:171383228-171383229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572141263	chr1:171383234-171383235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544628092	chr1:171383235-171383236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368847303	chr1:171383330-171383331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141378734	chr1:171383337-171383338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs578213703	chr1:171383341-171383342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545683297	chr1:171383422-171383423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150347005	chr1:171383444-171383445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2179880	chr1:171383462-171383463	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs7418672	chr1:171383503-171383504	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs7418675	chr1:171383527-171383528	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs531287395	chr1:171383555-171383556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549773332	chr1:171383651-171383652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143628613	chr1:171383664-171383665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571620099	chr1:171383694-171383695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532450376	chr1:171383725-171383726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189296669	chr1:171383775-171383776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs180957584	chr1:171383776-171383777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185833483	chr1:171383849-171383850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554327247	chr1:171383866-171383867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12401720	chr1:171383880-171383881	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs537924377	chr1:171383895-171383896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556535662	chr1:171383898-171383899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370457420	chr1:171383968-171383969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147158139	chr1:171383969-171383970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554549136	chr1:171383985-171383986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551272426	chr1:171384017-171384018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140425686	chr1:171384089-171384090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35124369	chr1:171384091-171384092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543281690	chr1:171384097-171384098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561304047	chr1:171384099-171384100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531459426	chr1:171384102-171384103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12410247	chr1:171384103-171384104	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs536930091	chr1:171384128-171384129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553643833	chr1:171384131-171384132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs71637406	chr1:171384167-171384168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs56973831	chr1:171384204-171384205	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs531936438	chr1:171384219-171384220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	20409316	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:171383000-171383200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:171383200-171390800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:171383400-171389600	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr1:171387000-171389600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr1:171387200-171387400	Enhancers	Placenta	Placenta
6	chr1:171387400-171388400	Weak transcription	Placenta	Placenta
7	chr1:171387800-171388000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:171387800-171388000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:171387800-171388000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:171387800-171388400	Enhancers	NHEK	skin
11	chr1:171388000-171388400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
12	chr1:171388000-171389800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr1:171388000-171390800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr1:171388000-171391000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr1:171388400-171388600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr1:171388400-171388800	Weak transcription	NHEK	skin
17	chr1:171388400-171389600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:171388400-171389600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr1:171388400-171389600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:171388400-171390200	Enhancers	Placenta	Placenta
21	chr1:171388600-171389000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr1:171388600-171391200	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr1:171388800-171390200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:171388800-171390400	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr1:171388800-171391000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr1:171388800-171391400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr1:171388800-171394600	Enhancers	NHEK	skin
28	chr1:171389000-171389200	Enhancers	NHDF-Ad	bronchial
29	chr1:171389000-171389800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr1:171389000-171390600	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr1:171389000-171390800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr1:171389000-171391000	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr1:171389000-171391400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr1:171389200-171391000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr1:171389200-171391800	Weak transcription	NHDF-Ad	bronchial
36	chr1:171389600-171389800	Enhancers	H9 Cell Line	embryonic stem cell
37	chr1:171389600-171389800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr1:171389600-171390000	Enhancers	Primary T cells fromperipheralblood	blood
39	chr1:171389600-171390000	Enhancers	Left Ventricle	heart
40	chr1:171389600-171390400	Enhancers	Primary T cells from cord blood	blood
41	chr1:171389600-171390400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr1:171389600-171390400	Enhancers	Stomach Mucosa	stomach
43	chr1:171389600-171390400	Enhancers	HMEC	breast
44	chr1:171389600-171390600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:171389600-171391200	Enhancers	H1 Cell Line	embryonic stem cell
46	chr1:171389600-171391200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr1:171389600-171391400	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr1:171389600-171391800	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr1:171389600-171391800	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr1:171389600-171394400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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