Variant report

Variant	nsv535210
Chromosome Location	chr1:175021780-175063160
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:292)
CpG islands
(count:733)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:292 , 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	ATF1	chr1:175041528-175041850	K562	blood:	n/a	n/a
2	ATF2	chr1:175041362-175041957	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr1:175041431-175041961	GM12878	blood:	n/a	n/a
4	ATF2	chr1:175041536-175041912	GM12878	blood:	n/a	n/a
5	ATF2	chr1:175041346-175041929	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr1:175041624-175041928	GM12878	blood:	n/a	n/a
7	CEBPB	chr1:175042200-175042563	Hela-S3	cervix:	n/a	chr1:175042378-175042389 chr1:175042376-175042387
8	CEBPB	chr1:175042212-175042561	IMR90	lung:	n/a	chr1:175042378-175042389 chr1:175042376-175042387
9	CEBPB	chr1:175042209-175042538	K562	blood:	n/a	chr1:175042378-175042389 chr1:175042376-175042387
10	CEBPB	chr1:175056470-175056717	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr1:175042191-175042486	HepG2	liver:	n/a	chr1:175042378-175042389 chr1:175042376-175042387
12	CEBPB	chr1:175042212-175042574	H1-hESC	embryonic stem cell:	n/a	chr1:175042378-175042389 chr1:175042376-175042387
13	CEBPB	chr1:175042260-175042431	HepG2	liver:	n/a	chr1:175042378-175042389 chr1:175042376-175042387
14	CEBPB	chr1:175042300-175042451	K562	blood:	n/a	chr1:175042378-175042389 chr1:175042376-175042387
15	CEBPB	chr1:175042203-175042583	HepG2	liver:	n/a	chr1:175042378-175042389 chr1:175042376-175042387
16	CEBPB	chr1:175042185-175042588	MCF-7	breast:	n/a	chr1:175042378-175042389 chr1:175042376-175042387
17	CEBPB	chr1:175042206-175042531	K562	blood:	n/a	chr1:175042378-175042389 chr1:175042376-175042387
18	CEBPB	chr1:175028766-175028803	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr1:175042205-175042568	A549	lung:	n/a	chr1:175042378-175042389 chr1:175042376-175042387
20	CHD2	chr1:175041508-175041941	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr1:175042288-175042290	GM12878	blood:	n/a	n/a
22	CTBP2	chr1:175042651-175043347	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr1:175042980-175043130	HFF-Myc	foreskin:	n/a	n/a
24	CTCF	chr1:175042740-175042890	GM12868	blood:	n/a	n/a
25	CTCF	chr1:175042750-175043155	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr1:175045380-175045530	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr1:175045300-175045450	NHEK	skin:	n/a	n/a
28	CTCF	chr1:175045433-175045557	GM12878	blood:	n/a	n/a
29	CTCF	chr1:175042932-175043105	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:175043009-175043039	K562	blood:	n/a	n/a
31	CTCF	chr1:175045420-175045570	GM12875	blood:	n/a	n/a
32	CTCF	chr1:175042900-175043050	GM12872	blood:	n/a	n/a
33	CTCF	chr1:175042986-175043041	GM13977	blood:	n/a	n/a
34	CTCF	chr1:175042985-175043081	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr1:175042960-175043110	HCT-116	colon:	n/a	n/a
36	CTCF	chr1:175034504-175034556	K562	blood:	n/a	n/a
37	CTCF	chr1:175045340-175045490	HepG2	liver:	n/a	n/a
38	CTCF	chr1:175042899-175043141	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr1:175045380-175045530	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr1:175042982-175043049	K562	blood:	n/a	n/a
41	CTCF	chr1:175042940-175043090	GM12864	blood:	n/a	n/a
42	CTCF	chr1:175043020-175043170	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr1:175042880-175043030	AG10803	skin:	n/a	n/a
44	CTCF	chr1:175045374-175045571	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:175042860-175043010	GM12864	blood:	n/a	n/a
46	CTCF	chr1:175042961-175043037	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr1:175043000-175043150	A549	lung:	n/a	n/a
48	CTCF	chr1:175045120-175045270	BE2_C	brain:	n/a	n/a
49	CTCF	chr1:175042980-175043130	GM12865	blood:	n/a	n/a
50	CTCF	chr1:175042900-175043050	GM12871	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:175035502-175035552	T-47D	breast:	n/a
2	chr1:175035502-175035552	T-47D	breast:	n/a
3	chr1:175048873-175048923	SK-N-SH	brain:	n/a
4	chr1:175048851-175048901	HPAEpiC	pulmonary alveolar:	n/a
5	chr1:175036986-175037036	H1-hESC	embryonic stem cell:	embryo
6	chr1:175046885-175046935	GM12878	blood:	n/a
7	chr1:175050479-175050529	HRE	kidney:	n/a
8	chr1:175051172-175051222	HIPEpiC	eye:	n/a
9	chr1:175044916-175044966	BE2_C	brain:	n/a
10	chr1:175048753-175048803	AoSMC	blood vessel:	n/a
11	chr1:175036687-175036737	AG09319	gingival:	n/a
12	chr1:175035502-175035552	HL-60	blood:	n/a
13	chr1:175036403-175036453	NH-A	brain:	n/a
14	chr1:175044916-175044966	AG04450	lung:	fetal
15	chr1:175051172-175051222	H1-hESC	embryonic stem cell:	embryo
16	chr1:175042297-175042347	SK-N-SH	brain:	n/a
17	chr1:175050479-175050529	AG04450	lung:	fetal
18	chr1:175036403-175036453	A549	lung:	n/a
19	chr1:175050479-175050529	AG04449	skin:	fetal
20	chr1:175050479-175050529	GM12878	blood:	n/a
21	chr1:175036687-175036737	ECC-1	luminal epithelium:	n/a
22	chr1:175035502-175035552	HUVEC	blood vessel:	n/a
23	chr1:175048873-175048923	Jurkat	blood:	n/a
24	chr1:175046885-175046935	HCM	heart:	n/a
25	chr1:175036403-175036453	HMEC	breast:	n/a
26	chr1:175035502-175035552	HRPEpiC	eye:	n/a
27	chr1:175044916-175044966	CMK	blood:	n/a
28	chr1:175036986-175037036	GM06990	blood:	n/a
29	chr1:175048873-175048923	AG04450	lung:	fetal
30	chr1:175042297-175042347	CMK	blood:	n/a
31	chr1:175048873-175048923	AoSMC	blood vessel:	n/a
32	chr1:175036986-175037036	ProgFib	skin:	n/a
33	chr1:175048753-175048803	BJ	skin:	n/a
34	chr1:175036986-175037036	PANC-1	pancreas:	n/a
35	chr1:175048753-175048803	ProgFib	skin:	n/a
36	chr1:175048873-175048923	NH-A	brain:	n/a
37	chr1:175048753-175048803	AG09309	skin:	n/a
38	chr1:175051172-175051222	SAEC	small airway:	n/a
39	chr1:175050479-175050529	K562	blood:	n/a
40	chr1:175046885-175046935	PrEC	prostate:	n/a
41	chr1:175048753-175048803	HepG2	liver:	n/a
42	chr1:175048753-175048803	GM12892	blood:	n/a
43	chr1:175048753-175048803	SAEC	small airway:	n/a
44	chr1:175035502-175035552	A549	lung:	n/a
45	chr1:175044916-175044966	A549	lung:	n/a
46	chr1:175042297-175042347	NH-A	brain:	n/a
47	chr1:175036403-175036453	Jurkat	blood:	n/a
48	chr1:175048851-175048901	NH-A	brain:	n/a
49	chr1:175035502-175035552	HNPCEpiC	eye:	n/a
50	chr1:175036403-175036453	MCF10A-Er-Src	breast:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:175048446..175050734-chr1:175051800..175053670,2	MCF-7	breast:
2	chr1:175061981..175063618-chr1:175064520..175066767,2	MCF-7	breast:
3	chr1:175033728..175036275-chr1:175037285..175039259,2	MCF-7	breast:
4	chr1:175050894..175052513-chr1:175093322..175096065,2	MCF-7	breast:
5	chr1:174998932..175000552-chr1:175032819..175035419,2	MCF-7	breast:
6	chr1:175058365..175061494-chr1:175062662..175065562,3	K562	blood:
7	chr1:175048686..175050495-chr1:175051528..175053707,2	K562	blood:
8	chr1:175041397..175042225-chr14:23298848..23299502,2	NB4	blood:
9	chr1:175028783..175030971-chr1:175038361..175041126,2	K562	blood:
10	chr1:175058271..175062583-chr1:175062770..175067990,6	K562	blood:
11	chr1:175048446..175050734-chr1:175051800..175053670,2	MCF-7	breast:
12	chr1:175047862..175049387-chr1:175064972..175066550,2	K562	blood:
13	chr1:175047887..175050312-chr1:175064283..175066550,2	K562	blood:
14	chr1:175041206..175043201-chr1:175056003..175057829,2	K562	blood:
15	chr1:175033728..175036275-chr1:175037285..175039259,2	MCF-7	breast:
16	chr1:175041206..175043201-chr1:175056003..175057829,2	K562	blood:
17	chr1:175037331..175039889-chr1:175047402..175050144,2	K562	blood:
18	chr1:175029280..175031926-chr1:175034008..175036600,2	MCF-7	breast:
19	chr1:175048686..175050495-chr1:175051528..175053707,2	K562	blood:
20	chr1:175045192..175046870-chr15:101253779..101256143,2	MCF-7	breast:
21	chr1:175037717..175040130-chr1:175044107..175046974,3	K562	blood:
22	chr1:174990991..174992562-chr1:175023200..175025789,2	MCF-7	breast:
23	chr1:175058271..175062583-chr1:175062770..175067990,6	K562	blood:
24	chr1:175037717..175040130-chr1:175044107..175046974,3	K562	blood:
25	chr1:175028783..175030971-chr1:175038361..175041126,2	K562	blood:
26	chr1:175058365..175061494-chr1:175062662..175065562,3	K562	blood:
27	chr1:175018453..175021258-chr1:175048643..175051325,2	MCF-7	breast:
28	chr1:175029280..175031926-chr1:175034008..175036600,2	MCF-7	breast:
29	chr1:175037331..175039889-chr1:175047402..175050144,2	K562	blood:

No data

Variant related genes	Relation type
TNN	TF binding region
TNN	CpG island
ENSG00000172590	chromatin interactions
ENSG00000155465	chromatin interactions
ENSG00000206659	chromatin interactions
ENSG00000120333	chromatin interactions

Extended variants
information (count: 1306 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1306 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2861107	chr1:175023224-175023225	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs542939821	chr1:175023239-175023240	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs150010633	chr1:175023241-175023242	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs576617007	chr1:175023243-175023244	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs370002821	chr1:175023285-175023286	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs561513187	chr1:175023322-175023323	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs375480726	chr1:175023344-175023345	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs112205171	chr1:175023345-175023346	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs113459505	chr1:175023348-175023349	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs564160752	chr1:175023353-175023354	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs11809097	chr1:175023367-175023368	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs183422001	chr1:175023403-175023404	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs540202344	chr1:175023425-175023426	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs560213620	chr1:175023438-175023439	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs79362515	chr1:175023457-175023458	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs558464121	chr1:175023514-175023515	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs145291203	chr1:175023526-175023527	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs568950578	chr1:175023539-175023540	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs531582710	chr1:175023542-175023543	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs370157167	chr1:175023646-175023647	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs537850165	chr1:175023669-175023670	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs59391278	chr1:175023707-175023708	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs149190316	chr1:175023726-175023727	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs77989459	chr1:175023759-175023760	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs116326515	chr1:175023760-175023761	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs567353691	chr1:175023860-175023861	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs536539538	chr1:175023882-175023883	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs55722817	chr1:175023886-175023887	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs56119006	chr1:175023888-175023889	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs192196405	chr1:175023897-175023898	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs184036748	chr1:175023933-175023934	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs75308228	chr1:175023951-175023952	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs545542380	chr1:175023997-175023998	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs558902947	chr1:175024063-175024064	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs577786021	chr1:175024066-175024067	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs145123077	chr1:175024101-175024102	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs560175189	chr1:175024105-175024106	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs71563267	chr1:175024147-175024148	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs73043034	chr1:175024149-175024150	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs74128558	chr1:175024176-175024177	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs574489705	chr1:175024178-175024179	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs553926878	chr1:175024198-175024199	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs539919662	chr1:175024278-175024279	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs140724394	chr1:175024353-175024354	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs187256014	chr1:175024388-175024389	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs531518349	chr1:175024397-175024398	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs551523710	chr1:175024398-175024399	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs564957543	chr1:175024450-175024451	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs527760898	chr1:175024514-175024515	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs573508461	chr1:175024534-175024535	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
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
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:175023800-175024200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr1:175023800-175024200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr1:175029800-175032000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:175031200-175032200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:175032200-175032400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:175036200-175036600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr1:175036200-175037200	Enhancers	Fetal Muscle Trunk	muscle
8	chr1:175036200-175037200	Enhancers	Fetal Muscle Leg	muscle
9	chr1:175036400-175037200	Enhancers	H1 Cell Line	embryonic stem cell
10	chr1:175036400-175037200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr1:175036400-175037600	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr1:175036600-175036800	Enhancers	Fetal Lung	lung
13	chr1:175036600-175037000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:175036600-175037200	Enhancers	Fetal Stomach	stomach
15	chr1:175036800-175037000	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr1:175036800-175037200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr1:175036800-175037400	Active TSS	Adipose Nuclei	Adipose
18	chr1:175036800-175041000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr1:175037000-175037200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr1:175037000-175037200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
21	chr1:175037200-175038600	Weak transcription	Fetal Muscle Leg	muscle
22	chr1:175037200-175040200	Weak transcription	Fetal Stomach	stomach
23	chr1:175037200-175040600	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr1:175037200-175041000	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr1:175037200-175041000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr1:175037200-175041000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr1:175037200-175041400	Weak transcription	Fetal Muscle Trunk	muscle
28	chr1:175037400-175039800	Weak transcription	Adipose Nuclei	Adipose
29	chr1:175037600-175038000	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr1:175038000-175041200	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr1:175038200-175041000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr1:175038600-175038800	Enhancers	Fetal Muscle Leg	muscle
33	chr1:175038600-175039000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr1:175038600-175041000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr1:175038800-175039000	Enhancers	H9 Cell Line	embryonic stem cell
36	chr1:175038800-175039000	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr1:175038800-175039200	Weak transcription	Fetal Muscle Leg	muscle
38	chr1:175038800-175039600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr1:175039000-175039400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr1:175039200-175040200	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr1:175039200-175041400	Enhancers	Fetal Muscle Leg	muscle
42	chr1:175039400-175039600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr1:175039400-175039600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr1:175039600-175040000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr1:175039600-175041200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr1:175039600-175041200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr1:175039800-175040000	Enhancers	Adipose Nuclei	Adipose
48	chr1:175039800-175041200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr1:175039800-175042400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:175039800-175046600	Enhancers	Primary hematopoietic stem cells short term culture	blood

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