Variant report

Variant	esv2762150
Chromosome Location	chr1:72271227-72395953
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:253)
CpG islands
(count:244)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:72384415-72384667	HepG2	liver:	n/a	chr1:72384650-72384666
2	BRCA1	chr1:72378156-72378200	GM12878	blood:	n/a	n/a
3	BRCA1	chr1:72391047-72391054	GM12878	blood:	n/a	n/a
4	CEBPB	chr1:72290106-72290476	IMR90	lung:	n/a	chr1:72290286-72290297
5	CEBPB	chr1:72353101-72353423	IMR90	lung:	n/a	chr1:72353242-72353253
6	CEBPB	chr1:72353163-72353392	HepG2	liver:	n/a	chr1:72353242-72353253
7	CEBPB	chr1:72353137-72353285	K562	blood:	n/a	chr1:72353242-72353253
8	CEBPB	chr1:72294559-72294726	HepG2	liver:	n/a	chr1:72294674-72294685
9	CEBPB	chr1:72326678-72327071	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:72353187-72353408	A549	lung:	n/a	chr1:72353242-72353253
11	CEBPB	chr1:72290198-72290381	H1-hESC	embryonic stem cell:	n/a	chr1:72290286-72290297
12	CEBPB	chr1:72290161-72290431	A549	lung:	n/a	chr1:72290286-72290297
13	CEBPB	chr1:72290112-72290442	HepG2	liver:	n/a	chr1:72290286-72290297
14	CEBPB	chr1:72326736-72327069	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:72322163-72322385	HepG2	liver:	n/a	chr1:72322284-72322295
16	CEBPB	chr1:72290139-72290394	K562	blood:	n/a	chr1:72290286-72290297
17	CEBPB	chr1:72274296-72274496	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPZ	chr1:72395734-72395783	HepG2	liver:	n/a	n/a
19	CTCF	chr1:72387880-72388030	BE2_C	brain:	n/a	n/a
20	CTCF	chr1:72387960-72388110	HEK293	kidney:	n/a	n/a
21	CTCF	chr1:72387984-72388085	MCF-7	breast:	n/a	n/a
22	CTCF	chr1:72387980-72388130	HRPEpiC	eye:	n/a	n/a
23	CTCF	chr1:72387999-72388098	HepG2	liver:	n/a	n/a
24	CTCF	chr1:72388000-72388150	BE2_C	brain:	n/a	n/a
25	CTCF	chr1:72277700-72277850	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr1:72388000-72388150	RPTEC	kidney:	n/a	n/a
27	CTCF	chr1:72387940-72388090	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr1:72387900-72388050	NHLF	lung:	n/a	n/a
29	CTCF	chr1:72387940-72388090	HEEpiC	esophagus:	n/a	n/a
30	CTCF	chr1:72387965-72388123	NHEK	skin:	n/a	n/a
31	CTCF	chr1:72387980-72388130	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr1:72277640-72277790	GM12875	blood:	n/a	n/a
33	CTCF	chr1:72388020-72388170	HAc	cerebellar:	n/a	n/a
34	CTCF	chr1:72388022-72388042	ProgFib	skin:	n/a	n/a
35	CTCF	chr1:72382695-72382753	MCF-7	breast:	n/a	n/a
36	CTCF	chr1:72387980-72388130	HMF	breast:	n/a	n/a
37	CTCF	chr1:72387920-72388070	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr1:72282820-72282970	GM12873	blood:	n/a	n/a
39	CTCF	chr1:72388033-72388087	MCF-7	breast:	n/a	n/a
40	CTCF	chr1:72387960-72388110	HepG2	liver:	n/a	n/a
41	CTCF	chr1:72382692-72382802	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:72387960-72388110	HRE	kidney:	n/a	n/a
43	CTCF	chr1:72387940-72388090	BJ	skin:	n/a	n/a
44	CTCF	chr1:72387738-72387771	GM13976	blood:	n/a	n/a
45	CTCF	chr1:72328657-72328672	LNCaP	prostate:	n/a	n/a
46	CTCF	chr1:72329920-72330070	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr1:72387880-72388030	NB4	blood:	n/a	n/a
48	CTCF	chr1:72284220-72284248	Lung_OC	lung:	n/a	n/a
49	CTCF	chr1:72387960-72388110	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr1:72277580-72277730	NHDF-neo	bronchial:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72354156-72354206	HAEpiC	amniotic membrane:	n/a
2	chr1:72302970-72303020	IMR90	lung:	fetal
3	chr1:72382645-72382695	LNCaP	prostate:	n/a
4	chr1:72354156-72354206	AG04449	skin:	fetal
5	chr1:72382835-72382885	NHDF-neo	bronchial:	n/a
6	chr1:72354156-72354206	K562	blood:	n/a
7	chr1:72354156-72354206	H1-hESC	embryonic stem cell:	embryo
8	chr1:72354156-72354206	HMEC	breast:	n/a
9	chr1:72302970-72303020	PrEC	prostate:	n/a
10	chr1:72302970-72303020	Hela-S3	cervix:	n/a
11	chr1:72354156-72354206	HL-60	blood:	n/a
12	chr1:72382835-72382885	Hepatocyte	liver:	n/a
13	chr1:72382835-72382885	GM12892	blood:	n/a
14	chr1:72382835-72382885	HCT-116	colon:	n/a
15	chr1:72382835-72382885	AoSMC	blood vessel:	n/a
16	chr1:72382835-72382885	T-47D	breast:	n/a
17	chr1:72302970-72303020	Hepatocyte	liver:	n/a
18	chr1:72382645-72382695	GM12878	blood:	n/a
19	chr1:72382645-72382695	HCT-116	colon:	n/a
20	chr1:72354156-72354206	NH-A	brain:	n/a
21	chr1:72354156-72354206	HIPEpiC	eye:	n/a
22	chr1:72302970-72303020	SKMC	muscle:	n/a
23	chr1:72354156-72354206	AG09319	gingival:	n/a
24	chr1:72382835-72382885	HRE	kidney:	n/a
25	chr1:72354156-72354206	Jurkat	blood:	n/a
26	chr1:72354156-72354206	HUVEC	blood vessel:	n/a
27	chr1:72382645-72382695	MCF10A-Er-Src	breast:	n/a
28	chr1:72354156-72354206	CMK	blood:	n/a
29	chr1:72354156-72354206	HNPCEpiC	eye:	n/a
30	chr1:72382645-72382695	HCM	heart:	n/a
31	chr1:72382835-72382885	NT2-D1	testis:	n/a
32	chr1:72302970-72303020	PFSK-1	brain:	n/a
33	chr1:72382645-72382695	Hela-S3	cervix:	n/a
34	chr1:72302970-72303020	A549	lung:	n/a
35	chr1:72382835-72382885	SK-N-SH	brain:	n/a
36	chr1:72354156-72354206	Hepatocyte	liver:	n/a
37	chr1:72382835-72382885	GM12878	blood:	n/a
38	chr1:72354156-72354206	HepG2	liver:	n/a
39	chr1:72354156-72354206	PANC-1	pancreas:	n/a
40	chr1:72354156-72354206	GM12892	blood:	n/a
41	chr1:72382835-72382885	BJ	skin:	n/a
42	chr1:72354156-72354206	SAEC	small airway:	n/a
43	chr1:72382835-72382885	HRPEpiC	eye:	n/a
44	chr1:72382645-72382695	HNPCEpiC	eye:	n/a
45	chr1:72302970-72303020	AoSMC	blood vessel:	n/a
46	chr1:72382835-72382885	HCF	heart:	n/a
47	chr1:72382645-72382695	PFSK-1	brain:	n/a
48	chr1:72382835-72382885	SK-N-SH_RA	brain:	n/a
49	chr1:72382835-72382885	PrEC	prostate:	n/a
50	chr1:72302970-72303020	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:72381957..72383996-chr1:72389950..72392631,2	K562	blood:
2	chr1:72381957..72383996-chr1:72389950..72392631,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZRANB2-1	chr1:72302663-72302695	ENSG00000228853.1

No data

Variant related genes	Relation type
NEGR1-IT1	TF binding region
NEGR1-IT1	CpG island

Extended variants
information (count: 3581 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:3581 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574722823	chr1:72274009-72274010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs369829763	chr1:72274011-72274012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs72948041	chr1:72274034-72274035	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs185977184	chr1:72274045-72274046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532211379	chr1:72274081-72274082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs552308968	chr1:72274104-72274105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373481678	chr1:72274115-72274116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148025761	chr1:72274145-72274146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs534439456	chr1:72274153-72274154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs72678965	chr1:72274176-72274177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551297752	chr1:72274177-72274178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536568437	chr1:72274185-72274186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556488887	chr1:72274214-72274215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189708055	chr1:72274253-72274254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs371212363	chr1:72274256-72274257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557156013	chr1:72274289-72274290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181241281	chr1:72274291-72274292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558673908	chr1:72274323-72274324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs571900585	chr1:72274345-72274346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs186025947	chr1:72274362-72274363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561001050	chr1:72274375-72274376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190487162	chr1:72274382-72274383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373205354	chr1:72274413-72274414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182721290	chr1:72274415-72274416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149184521	chr1:72274420-72274421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs115713777	chr1:72274435-72274436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545466902	chr1:72274448-72274449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186290887	chr1:72274454-72274455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs377375848	chr1:72274456-72274457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532145221	chr1:72274458-72274459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs12141391	chr1:72274473-72274474	Enhancers	n/a	n/a	Overlapped CNVs	disease
32	rs559528292	chr1:72274565-72274566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79164022	chr1:72274584-72274585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547945051	chr1:72274586-72274587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182648965	chr1:72274621-72274622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536912828	chr1:72274688-72274689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550210646	chr1:72274732-72274733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs569711897	chr1:72274748-72274749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201398611	chr1:72274778-72274779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77451356	chr1:72274803-72274804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs572234633	chr1:72274809-72274810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534811733	chr1:72274855-72274856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554715775	chr1:72274858-72274859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs57227393	chr1:72274874-72274875	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs543652826	chr1:72274896-72274897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs199699398	chr1:72274919-72274920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539497699	chr1:72274978-72274979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191311579	chr1:72274984-72274985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576897385	chr1:72275010-72275011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141741717	chr1:72275132-72275133	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
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
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
body mass index	19812545	CNVD
Obesity	20935630	CNVD
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD
Attention deficit hyperactivity disorder	22138692	CNVD
Recurrent pregnancy loss	19789632	CNVD

Chromatin state (count:399 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72274000-72275600	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr1:72280800-72281000	Enhancers	Dnd41	blood
3	chr1:72281200-72282400	Weak transcription	Dnd41	blood
4	chr1:72282400-72283200	Enhancers	Dnd41	blood
5	chr1:72282600-72283000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:72282600-72283200	Enhancers	Stomach Smooth Muscle	stomach
7	chr1:72282800-72283400	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr1:72284600-72289400	Weak transcription	Primary hematopoietic stem cells	blood
9	chr1:72284800-72285000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:72285000-72288600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr1:72285400-72286200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr1:72285600-72286000	Enhancers	Brain Substantia Nigra	brain
13	chr1:72287200-72292600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr1:72287800-72288000	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr1:72288200-72289600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr1:72288600-72289400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:72289000-72290600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr1:72289400-72289800	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr1:72289400-72290000	Enhancers	Primary hematopoietic stem cells	blood
20	chr1:72289400-72290000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr1:72289600-72290000	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr1:72289800-72294200	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr1:72290000-72290400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr1:72290000-72292200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr1:72290400-72291800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:72290600-72292000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr1:72290800-72291200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr1:72291200-72291600	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr1:72291600-72293600	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr1:72291800-72292200	Enhancers	Brain Cingulate Gyrus	brain
31	chr1:72291800-72294600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr1:72291800-72294800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr1:72291800-72294800	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr1:72292000-72293000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:72292000-72293200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr1:72292000-72293200	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr1:72292000-72293200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr1:72292200-72292600	Enhancers	H1 Cell Line	embryonic stem cell
39	chr1:72292200-72293200	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr1:72292200-72299400	Weak transcription	Brain Cingulate Gyrus	brain
41	chr1:72292400-72293400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:72292600-72293200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr1:72292600-72293200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr1:72292600-72294400	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr1:72292600-72294800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr1:72292600-72294800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr1:72293000-72293200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr1:72293000-72293200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr1:72293000-72293200	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr1:72293000-72293200	Enhancers	Brain Substantia Nigra	brain

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