Variant report

Variant	nsv871024
Chromosome Location	chr1:71088106-71169865
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:722)
CpG islands
(count:61)
Chromatin interactive
region (count:31)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:722 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:71141392-71142388	K562	blood:	n/a	n/a
2	ARID3A	chr1:71140378-71141135	K562	blood:	n/a	n/a
3	ARID3A	chr1:71142688-71142734	K562	blood:	n/a	n/a
4	ARID3A	chr1:71137685-71137808	K562	blood:	n/a	n/a
5	ATF1	chr1:71150917-71151343	K562	blood:	n/a	n/a
6	ATF1	chr1:71141402-71141882	K562	blood:	n/a	n/a
7	ATF1	chr1:71132571-71132808	K562	blood:	n/a	n/a
8	ATF1	chr1:71140608-71141142	K562	blood:	n/a	n/a
9	ATF2	chr1:71150896-71151421	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr1:71150927-71151340	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr1:71151025-71151325	K562	blood:	n/a	n/a
12	ATF3	chr1:71141414-71141877	K562	blood:	n/a	n/a
13	BACH1	chr1:71141312-71141770	K562	blood:	n/a	n/a
14	BACH1	chr1:71137894-71137898	K562	blood:	n/a	n/a
15	BATF	chr1:71141392-71141709	GM12878	blood:	n/a	n/a
16	BCL11A	chr1:71141519-71141703	GM12878	blood:	n/a	n/a
17	BHLHE40	chr1:71140676-71141146	K562	blood:	n/a	n/a
18	BHLHE40	chr1:71151096-71151322	K562	blood:	n/a	n/a
19	BHLHE40	chr1:71141408-71141900	K562	blood:	n/a	n/a
20	CBX3	chr1:71140588-71142260	K562	blood:	n/a	n/a
21	CBX3	chr1:71150862-71151380	K562	blood:	n/a	n/a
22	CBX3	chr1:71092850-71093427	K562	blood:	n/a	n/a
23	CBX3	chr1:71141397-71141875	K562	blood:	n/a	n/a
24	CBX3	chr1:71093472-71093954	K562	blood:	n/a	n/a
25	CCNT2	chr1:71140407-71141161	K562	blood:	n/a	n/a
26	CCNT2	chr1:71162869-71163199	K562	blood:	n/a	n/a
27	CCNT2	chr1:71141437-71141967	K562	blood:	n/a	n/a
28	CEBPB	chr1:71140465-71140575	HepG2	liver:	n/a	chr1:71140507-71140518 chr1:71140509-71140518 chr1:71140508-71140519
29	CEBPB	chr1:71141448-71142103	K562	blood:	n/a	n/a
30	CEBPB	chr1:71150955-71151455	A549	lung:	n/a	n/a
31	CEBPB	chr1:71164932-71165201	K562	blood:	n/a	chr1:71164992-71165003 chr1:71164994-71165005 chr1:71164992-71165005 chr1:71164994-71165003
32	CEBPB	chr1:71145414-71145703	HepG2	liver:	n/a	chr1:71145548-71145559
33	CEBPB	chr1:71150983-71151472	MCF-7	breast:	n/a	n/a
34	CEBPB	chr1:71093610-71093911	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr1:71127186-71127483	IMR90	lung:	n/a	chr1:71127318-71127329
36	CEBPB	chr1:71151108-71151297	HepG2	liver:	n/a	n/a
37	CEBPB	chr1:71164894-71165149	HepG2	liver:	n/a	chr1:71164992-71165003 chr1:71164994-71165005 chr1:71164992-71165005 chr1:71164994-71165003 chr1:71164921-71164929
38	CEBPB	chr1:71151025-71151414	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr1:71150970-71151439	K562	blood:	n/a	n/a
40	CEBPB	chr1:71151046-71151388	A549	lung:	n/a	n/a
41	CEBPB	chr1:71151030-71151410	IMR90	lung:	n/a	n/a
42	CEBPB	chr1:71105501-71105717	K562	blood:	n/a	chr1:71105618-71105629
43	CEBPB	chr1:71110812-71110949	K562	blood:	n/a	n/a
44	CEBPB	chr1:71151117-71151332	K562	blood:	n/a	n/a
45	CEBPB	chr1:71138572-71138673	K562	blood:	n/a	n/a
46	CEBPB	chr1:71105483-71105770	HepG2	liver:	n/a	chr1:71105618-71105629
47	CEBPB	chr1:71151033-71151409	A549	lung:	n/a	n/a
48	CEBPB	chr1:71141254-71142056	K562	blood:	n/a	n/a
49	CEBPB	chr1:71093638-71093872	K562	blood:	n/a	n/a
50	CEBPB	chr1:71150953-71151457	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:71140689-71140739	HCT-116	colon:	n/a
2	chr1:71140689-71140739	RPTEC	kidney:	n/a
3	chr1:71140689-71140739	GM12891	blood:	n/a
4	chr1:71140689-71140739	SK-N-SH	brain:	n/a
5	chr1:71140689-71140739	AG04449	skin:	fetal
6	chr1:71140689-71140739	CMK	blood:	n/a
7	chr1:71140689-71140739	HL-60	blood:	n/a
8	chr1:71140689-71140739	Hela-S3	cervix:	n/a
9	chr1:71140689-71140739	HIPEpiC	eye:	n/a
10	chr1:71140689-71140739	A549	lung:	n/a
11	chr1:71140689-71140739	ovcar-3	ovarian:	n/a
12	chr1:71140689-71140739	Jurkat	blood:	n/a
13	chr1:71140689-71140739	GM12878	blood:	n/a
14	chr1:71140689-71140739	K562	blood:	n/a
15	chr1:71140689-71140739	HCM	heart:	n/a
16	chr1:71140689-71140739	NHBE	bronchial:	n/a
17	chr1:71140689-71140739	SK-N-MC	brain:	n/a
18	chr1:71140689-71140739	GM06990	blood:	n/a
19	chr1:71140689-71140739	GM12892	blood:	n/a
20	chr1:71140689-71140739	HPAEpiC	pulmonary alveolar:	n/a
21	chr1:71140689-71140739	HCF	heart:	n/a
22	chr1:71140689-71140739	HRPEpiC	eye:	n/a
23	chr1:71140689-71140739	NHDF-neo	bronchial:	n/a
24	chr1:71140689-71140739	AG04450	lung:	fetal
25	chr1:71140689-71140739	HCPEpiC	choroid plexus:	n/a
26	chr1:71140689-71140739	HEEpiC	esophagus:	n/a
27	chr1:71140689-71140739	LNCaP	prostate:	n/a
28	chr1:71140689-71140739	IMR90	lung:	fetal
29	chr1:71140689-71140739	HEK293	kidney:	embryo
30	chr1:71140689-71140739	SAEC	small airway:	n/a
31	chr1:71140689-71140739	AG09309	skin:	n/a
32	chr1:71140689-71140739	HepG2	liver:	n/a
33	chr1:71140689-71140739	Caco-2	colon:	n/a
34	chr1:71140689-71140739	SK-N-SH_RA	brain:	n/a
35	chr1:71140689-71140739	Hepatocyte	liver:	n/a
36	chr1:71140689-71140739	HNPCEpiC	eye:	n/a
37	chr1:71140689-71140739	MCF10A-Er-Src	breast:	n/a
38	chr1:71140689-71140739	HRE	kidney:	n/a
39	chr1:71140689-71140739	HMEC	breast:	n/a
40	chr1:71140689-71140739	PrEC	prostate:	n/a
41	chr1:71140689-71140739	NT2-D1	testis:	n/a
42	chr1:71140689-71140739	PFSK-1	brain:	n/a
43	chr1:71140689-71140739	AG09319	gingival:	n/a
44	chr1:71140689-71140739	U87	brain:	n/a
45	chr1:71140689-71140739	T-47D	breast:	n/a
46	chr1:71140689-71140739	HRCEpiC	kidney:	n/a
47	chr1:71140689-71140739	HAEpiC	amniotic membrane:	n/a
48	chr1:71140689-71140739	BE2_C	brain:	n/a
49	chr1:71140689-71140739	BJ	skin:	n/a
50	chr1:71140689-71140739	H1-hESC	embryonic stem cell:	embryo

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:71151875..71153829-chr1:71156750..71159321,2	K562	blood:
2	chr1:71155714..71157917-chr1:71158810..71160998,2	K562	blood:
3	chr1:71139809..71142590-chr1:71513361..71515256,2	K562	blood:
4	chr1:71155714..71157917-chr1:71158810..71160998,2	K562	blood:
5	chr1:71092364..71093880-chr1:71095462..71097531,2	K562	blood:
6	chr1:71095861..71098505-chr1:71102216..71104078,2	K562	blood:
7	chr1:71164353..71167028-chr1:71509072..71511419,2	K562	blood:
8	chr1:71146129..71148659-chr1:71148897..71151242,2	K562	blood:
9	chr1:71139654..71142192-chr1:71144510..71147443,2	MCF-7	breast:
10	chr1:71131135..71133902-chr1:71140118..71142284,2	K562	blood:
11	chr1:71153691..71155593-chr1:71164333..71165915,2	K562	blood:
12	chr1:71150946..71151636-chr1:71515358..71516367,3	K562	blood:
13	chr1:71093858..71095458-chr1:71099227..71103372,3	K562	blood:
14	chr1:71163220..71166214-chr1:71167736..71169797,2	K562	blood:
15	chr1:71092364..71093880-chr1:71095462..71097531,2	K562	blood:
16	chr1:71150765..71151639-chr1:71429287..71429792,2	MCF-7	breast:
17	chr1:71139654..71142192-chr1:71144510..71147443,2	MCF-7	breast:
18	chr1:71151875..71153829-chr1:71156750..71159321,2	K562	blood:
19	chr1:71140625..71143147-chr1:71147219..71151401,4	K562	blood:
20	chr1:71146129..71148659-chr1:71148897..71151242,2	K562	blood:
21	chr1:71163220..71166214-chr1:71167736..71169797,2	K562	blood:
22	chr1:70818747..70820736-chr1:71127500..71130430,2	K562	blood:
23	chr1:71113661..71115986-chr1:71510232..71513062,3	K562	blood:
24	chr1:71153691..71155593-chr1:71164333..71165915,2	K562	blood:
25	chr1:71140625..71143147-chr1:71147219..71151401,4	K562	blood:
26	chr1:71151065..71151734-chr1:71515451..71516000,2	MCF-7	breast:
27	chr1:71093858..71095458-chr1:71099227..71103372,3	K562	blood:
28	chr1:71095861..71098505-chr1:71102216..71104078,2	K562	blood:
29	chr1:71124304..71124824-chr2:161134910..161135854,3	MCF-7	breast:
30	chr1:71131135..71133902-chr1:71140118..71142284,2	K562	blood:
31	chr1:71128661..71130608-chr1:71489552..71491952,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTH-1	chr1:71169373-71169486	NONHSAT003864
2	lnc-PTGER3-2	chr1:71110666-71110727	XLOC_000868
3	lnc-PTGER3-9	chr1:71126340-71126948	NONHSAT003863
4	lnc-PTGER3-2	chr1:71114347-71114581	XLOC_000868

No data

Variant related genes	Relation type
ENSG00000229051	TF binding region
CASP3P1	TF binding region
ENSG00000229051	CpG island
CASP3P1	CpG island
ENSG00000118454	chromatin interactions
ENSG00000197568	chromatin interactions
ENSG00000050628	chromatin interactions
ENSG00000235079	chromatin interactions

Extended variants
information (count: 1294 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:1294 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189992127	chr1:71094813-71094814	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs181251646	chr1:71094829-71094830	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs538441900	chr1:71094877-71094878	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs535850313	chr1:71094889-71094890	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs538028788	chr1:71094890-71094891	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs566031181	chr1:71094892-71094893	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs571929558	chr1:71094897-71094898	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs7525909	chr1:71094903-71094904	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs553393213	chr1:71094998-71094999	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs573299277	chr1:71095026-71095027	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs535799421	chr1:71095034-71095035	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs556232875	chr1:71095052-71095053	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs148998344	chr1:71095055-71095056	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs576024719	chr1:71095057-71095058	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs368286569	chr1:71095058-71095059	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs61778672	chr1:71095061-71095062	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs186283506	chr1:71095091-71095092	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs148210684	chr1:71095121-71095122	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs77457948	chr1:71095168-71095169	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs12087314	chr1:71095174-71095175	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs529306364	chr1:71095191-71095192	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs191933059	chr1:71098844-71098845	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs573550609	chr1:71098850-71098851	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs11584190	chr1:71098885-71098886	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs183349987	chr1:71098919-71098920	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs571716693	chr1:71098931-71098932	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs72684705	chr1:71098941-71098942	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs149655390	chr1:71098972-71098973	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs374199264	chr1:71098996-71098997	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs189178727	chr1:71099089-71099090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs193076869	chr1:71099102-71099103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs201440562	chr1:71099165-71099166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs78732925	chr1:71099166-71099167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546353453	chr1:71099171-71099172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183799498	chr1:71110720-71110721	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs545230522	chr1:71111621-71111622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559096335	chr1:71111660-71111661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369093713	chr1:71111704-71111705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569325220	chr1:71111718-71111719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12140094	chr1:71111771-71111772	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs111356844	chr1:71111848-71111849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561380473	chr1:71111934-71111935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529726241	chr1:71111953-71111954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28415396	chr1:71111969-71111970	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs563402951	chr1:71112007-71112008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530588346	chr1:71112017-71112018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377509013	chr1:71112057-71112058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543922510	chr1:71112058-71112059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186216401	chr1:71112061-71112062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563613248	chr1:71112067-71112068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Chordoma	21215367	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:175 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71094800-71095200	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr1:71098800-71099000	Bivalent Enhancer	Left Ventricle	heart
3	chr1:71098800-71099200	Enhancers	Brain Substantia Nigra	brain
4	chr1:71111600-71115400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr1:71115400-71116000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr1:71115400-71116200	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr1:71115400-71116800	Enhancers	Fetal Heart	heart
8	chr1:71119800-71120000	Enhancers	NHDF-Ad	bronchial
9	chr1:71120200-71121800	Weak transcription	NHDF-Ad	bronchial
10	chr1:71121400-71122800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:71121800-71122600	Enhancers	NHDF-Ad	bronchial
12	chr1:71129600-71130200	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr1:71131400-71132400	Enhancers	Fetal Lung	lung
14	chr1:71132000-71134600	Enhancers	Fetal Heart	heart
15	chr1:71132200-71132400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:71132200-71132400	Enhancers	Fetal Kidney	kidney
17	chr1:71132200-71132600	Enhancers	Esophagus	oesophagus
18	chr1:71132200-71132800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr1:71132200-71132800	Enhancers	Gastric	stomach
20	chr1:71132200-71132800	Enhancers	Left Ventricle	heart
21	chr1:71132200-71132800	Enhancers	Lung	lung
22	chr1:71132200-71132800	Enhancers	Right Atrium	heart
23	chr1:71132200-71133000	Enhancers	Aorta	Aorta
24	chr1:71132200-71133000	Enhancers	Pancreas	Pancrea
25	chr1:71132200-71133800	Enhancers	Rectal Smooth Muscle	rectum
26	chr1:71132400-71132600	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr1:71132400-71133200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr1:71132400-71137600	Weak transcription	Fetal Lung	lung
29	chr1:71132600-71133400	Enhancers	K562	blood
30	chr1:71132800-71133800	Weak transcription	Left Ventricle	heart
31	chr1:71132800-71133800	Weak transcription	Right Atrium	heart
32	chr1:71132800-71136800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:71132800-71141000	Weak transcription	Gastric	stomach
34	chr1:71133000-71133400	Weak transcription	Pancreas	Pancrea
35	chr1:71133000-71133600	Weak transcription	Aorta	Aorta
36	chr1:71133200-71133800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:71133400-71134000	Enhancers	Pancreas	Pancrea
38	chr1:71133400-71136400	Weak transcription	K562	blood
39	chr1:71133600-71133800	Enhancers	Aorta	Aorta
40	chr1:71133600-71134000	Enhancers	NHDF-Ad	bronchial
41	chr1:71133600-71134400	Enhancers	Fetal Stomach	stomach
42	chr1:71133800-71134000	Enhancers	Left Ventricle	heart
43	chr1:71133800-71134200	Enhancers	Right Atrium	heart
44	chr1:71133800-71137600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:71133800-71138600	Weak transcription	Aorta	Aorta
46	chr1:71134000-71140600	Weak transcription	Pancreas	Pancrea
47	chr1:71134400-71136400	Weak transcription	Fetal Stomach	stomach
48	chr1:71134600-71135800	Weak transcription	Fetal Heart	heart
49	chr1:71135800-71136200	Enhancers	Fetal Heart	heart
50	chr1:71136200-71140400	Weak transcription	Fetal Heart	heart

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