Variant report

Variant	nsv3454
Chromosome Location	chr1:170134880-170149447
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	chr1:170143550-170143634	K562	blood:	n/a	n/a
2	ATF1	chr1:170135671-170135892	K562	blood:	n/a	n/a
3	ATF1	chr1:170137401-170137867	K562	blood:	n/a	n/a
4	ATF1	chr1:170144260-170144588	K562	blood:	n/a	n/a
5	BHLHE40	chr1:170136558-170136684	K562	blood:	n/a	n/a
6	BRCA1	chr1:170144247-170144445	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:170137550-170137859	IMR90	lung:	n/a	n/a
8	CEBPB	chr1:170144215-170144493	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr1:170137361-170138049	HCT-116	colon:	n/a	n/a
10	CEBPB	chr1:170137492-170137965	HCT-116	colon:	n/a	n/a
11	CEBPB	chr1:170139414-170139462	HepG2	liver:	n/a	chr1:170139436-170139447
12	CEBPB	chr1:170139313-170139599	Hela-S3	cervix:	n/a	chr1:170139436-170139447
13	CEBPB	chr1:170139393-170139576	A549	lung:	n/a	chr1:170139436-170139447
14	CEBPB	chr1:170137099-170137969	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:170144219-170144436	IMR90	lung:	n/a	n/a
16	CHD2	chr1:170137263-170137862	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr1:170136861-170136888	A549	lung:	n/a	n/a
18	CTCF	chr1:170136904-170136920	Fibrobl	skin:	n/a	n/a
19	CTCF	chr1:170138863-170138886	GM20000	blood:	n/a	n/a
20	CTCF	chr1:170136921-170136939	Fibrobl	skin:	n/a	n/a
21	E2F4	chr1:170146091-170146385	MCF10A-Er-Src	breast:	n/a	n/a
22	ELF1	chr1:170143596-170143784	HepG2	liver:	n/a	n/a
23	EP300	chr1:170144592-170145056	SK-N-SH_RA	brain:	n/a	n/a
24	EP300	chr1:170137602-170137685	GM12878	blood:	n/a	chr1:170137623-170137637 chr1:170137668-170137682
25	EP300	chr1:170137416-170137920	K562	blood:	n/a	chr1:170137704-170137712 chr1:170137528-170137537 chr1:170137524-170137538 chr1:170137623-170137637 chr1:170137668-170137682
26	EP300	chr1:170144577-170144944	SK-N-SH_RA	brain:	n/a	n/a
27	EP300	chr1:170137312-170137915	Hela-S3	cervix:	n/a	chr1:170137704-170137712 chr1:170137387-170137401 chr1:170137528-170137537 chr1:170137385-170137399 chr1:170137524-170137538 chr1:170137623-170137637 chr1:170137668-170137682 chr1:170137391-170137405
28	GATA3	chr1:170137334-170137989	SK-N-SH	brain:	n/a	chr1:170137720-170137736
29	IRF1	chr1:170137508-170137805	K562	blood:	n/a	chr1:170137666-170137677 chr1:170137665-170137676 chr1:170137666-170137680 chr1:170137666-170137679 chr1:170137663-170137677 chr1:170137661-170137678 chr1:170137661-170137682 chr1:170137667-170137677 chr1:170137666-170137679 chr1:170137665-170137679 chr1:170137666-170137679 chr1:170137667-170137681 chr1:170137669-170137683 chr1:170137664-170137678 chr1:170137665-170137685
30	IRF1	chr1:170137475-170137821	K562	blood:	n/a	chr1:170137666-170137677 chr1:170137665-170137676 chr1:170137666-170137680 chr1:170137666-170137679 chr1:170137663-170137677 chr1:170137661-170137678 chr1:170137661-170137682 chr1:170137667-170137677 chr1:170137666-170137679 chr1:170137665-170137679 chr1:170137666-170137679 chr1:170137667-170137681 chr1:170137669-170137683 chr1:170137664-170137678 chr1:170137665-170137685
31	IRF1	chr1:170137424-170137861	K562	blood:	n/a	chr1:170137666-170137677 chr1:170137665-170137676 chr1:170137666-170137680 chr1:170137666-170137679 chr1:170137663-170137677 chr1:170137661-170137678 chr1:170137661-170137682 chr1:170137667-170137677 chr1:170137666-170137679 chr1:170137665-170137679 chr1:170137666-170137679 chr1:170137667-170137681 chr1:170137669-170137683 chr1:170137664-170137678 chr1:170137665-170137685
32	JUN	chr1:170137720-170137757	HepG2	liver:	n/a	n/a
33	JUND	chr1:170137505-170137848	K562	blood:	n/a	n/a
34	JUND	chr1:170144405-170144507	HepG2	liver:	n/a	n/a
35	JUND	chr1:170144302-170144519	K562	blood:	n/a	n/a
36	JUND	chr1:170135744-170135969	HepG2	liver:	n/a	n/a
37	JUND	chr1:170136668-170136852	K562	blood:	n/a	n/a
38	KAP1	chr1:170137418-170137840	U2OS	brain:	n/a	n/a
39	KAP1	chr1:170137340-170137922	HEK293	kidney:	n/a	n/a
40	MAZ	chr1:170137525-170137725	K562	blood:	n/a	n/a
41	MEF2A	chr1:170137413-170137925	SK-N-SH	brain:	n/a	chr1:170137831-170137842 chr1:170137674-170137688 chr1:170137829-170137844 chr1:170137827-170137848
42	MXI1	chr1:170137258-170137271	GM12878	blood:	n/a	n/a
43	PBX3	chr1:170144591-170145024	SK-N-SH	brain:	n/a	n/a
44	POLR2A	chr1:170144076-170145260	PFSK-1	brain:	n/a	n/a
45	POLR2A	chr1:170139051-170139143	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr1:170137367-170137880	PFSK-1	brain:	n/a	n/a
47	POLR2A	chr1:170143175-170143288	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr1:170136795-170136968	MCF-7	breast:	n/a	n/a
49	PRDM1	chr1:170137426-170137895	Hela-S3	cervix:	n/a	chr1:170137665-170137678 chr1:170137663-170137678
50	RCOR1	chr1:170136550-170136848	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:170136883-170136933	SK-N-MC	brain:	n/a
2	chr1:170136883-170136933	Jurkat	blood:	n/a
3	chr1:170136883-170136933	NT2-D1	testis:	n/a
4	chr1:170136883-170136933	A549	lung:	n/a
5	chr1:170136883-170136933	HRCEpiC	kidney:	n/a
6	chr1:170136883-170136933	NHBE	bronchial:	n/a
7	chr1:170136883-170136933	HepG2	liver:	n/a
8	chr1:170136883-170136933	T-47D	breast:	n/a
9	chr1:170136883-170136933	ProgFib	skin:	n/a
10	chr1:170136883-170136933	LNCaP	prostate:	n/a
11	chr1:170136883-170136933	SAEC	small airway:	n/a
12	chr1:170136883-170136933	K562	blood:	n/a
13	chr1:170136883-170136933	HL-60	blood:	n/a
14	chr1:170136883-170136933	GM12892	blood:	n/a
15	chr1:170136883-170136933	NH-A	brain:	n/a
16	chr1:170136883-170136933	HIPEpiC	eye:	n/a
17	chr1:170136883-170136933	NB4	blood:	n/a
18	chr1:170136883-170136933	U87	brain:	n/a
19	chr1:170136883-170136933	HCM	heart:	n/a
20	chr1:170136883-170136933	SKMC	muscle:	n/a
21	chr1:170136883-170136933	HPAEpiC	pulmonary alveolar:	n/a
22	chr1:170136883-170136933	HRPEpiC	eye:	n/a
23	chr1:170136883-170136933	BE2_C	brain:	n/a
24	chr1:170136883-170136933	HMEC	breast:	n/a
25	chr1:170136883-170136933	AG09319	gingival:	n/a
26	chr1:170136883-170136933	SK-N-SH_RA	brain:	n/a
27	chr1:170136883-170136933	ovcar-3	ovarian:	n/a
28	chr1:170136883-170136933	HUVEC	blood vessel:	n/a
29	chr1:170136883-170136933	AG04449	skin:	fetal
30	chr1:170136883-170136933	NHDF-neo	bronchial:	n/a
31	chr1:170136883-170136933	ECC-1	luminal epithelium:	n/a
32	chr1:170136883-170136933	GM12878	blood:	n/a
33	chr1:170136883-170136933	GM19239	blood:	n/a
34	chr1:170136883-170136933	BJ	skin:	n/a
35	chr1:170136883-170136933	PrEC	prostate:	n/a
36	chr1:170136883-170136933	PFSK-1	brain:	n/a
37	chr1:170136883-170136933	HAEpiC	amniotic membrane:	n/a
38	chr1:170136883-170136933	HEK293	kidney:	embryo
39	chr1:170136883-170136933	HNPCEpiC	eye:	n/a
40	chr1:170136883-170136933	PANC-1	pancreas:	n/a
41	chr1:170136883-170136933	HCF	heart:	n/a
42	chr1:170136883-170136933	SK-N-SH	brain:	n/a
43	chr1:170136883-170136933	CMK	blood:	n/a
44	chr1:170136883-170136933	MCF-7	breast:	n/a
45	chr1:170136883-170136933	Caco-2	colon:	n/a
46	chr1:170136883-170136933	AoSMC	blood vessel:	n/a
47	chr1:170136883-170136933	AG09309	skin:	n/a
48	chr1:170136883-170136933	HCT-116	colon:	n/a
49	chr1:170136883-170136933	MCF10A-Er-Src	breast:	n/a
50	chr1:170136883-170136933	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:170129471..170132945-chr1:170134793..170138535,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-METTL11B-1	chr1:170143657-170143847	NONHSAT007492
2	lnc-METTL11B-1	chr1:170143544-170143847	ENSG00000233985

Variant related genes	Relation type
ENSG00000233985	TF binding region
ENSG00000233985	CpG island

Extended variants
information (count: 309 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10800502	chr1:170134923-170134924	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs370280391	chr1:170134980-170134981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs66602590	chr1:170134981-170134982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76093279	chr1:170134982-170134983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs3040075	chr1:170134992-170134993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs398053517	chr1:170134993-170134994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs80308788	chr1:170134994-170134995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534960166	chr1:170135002-170135003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533979051	chr1:170135153-170135154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201610598	chr1:170135197-170135198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549448249	chr1:170135208-170135209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553078744	chr1:170135249-170135250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373817994	chr1:170135262-170135263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs367661121	chr1:170135266-170135267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs55662544	chr1:170135279-170135280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs59952169	chr1:170135280-170135281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs58785002	chr1:170135281-170135282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200981198	chr1:170135282-170135283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs55749121	chr1:170135285-170135286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113990833	chr1:170135287-170135288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs3040077	chr1:170135298-170135299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12062686	chr1:170135301-170135302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569934657	chr1:170135303-170135304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551977219	chr1:170135372-170135373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574805829	chr1:170135373-170135374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs12744233	chr1:170135425-170135426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111301492	chr1:170135430-170135431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111283972	chr1:170135434-170135435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11461930	chr1:170135447-170135448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10919313	chr1:170135468-170135469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558018847	chr1:170135470-170135471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539352852	chr1:170135507-170135508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576572	chr1:170135510-170135511	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs543760912	chr1:170135524-170135525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368499041	chr1:170135560-170135561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542290466	chr1:170135586-170135587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561014683	chr1:170135601-170135602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs61825691	chr1:170135608-170135609	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs370161493	chr1:170135625-170135626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs367930467	chr1:170135645-170135646	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183687510	chr1:170135646-170135647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564747277	chr1:170135651-170135652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375632420	chr1:170135656-170135657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6427234	chr1:170135669-170135670	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs372010040	chr1:170135681-170135682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs41272485	chr1:170135693-170135694	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs535550660	chr1:170135699-170135700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs6427235	chr1:170135760-170135761	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs6669514	chr1:170135765-170135766	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs369875685	chr1:170135776-170135777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Glioblastoma multiforme	21080181	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
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
Breast cancer	21509527	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:170126200-170135600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:170132000-170135800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr1:170132200-170136600	Weak transcription	Ovary	ovary
4	chr1:170132200-170136800	Weak transcription	Fetal Muscle Leg	muscle
5	chr1:170132400-170136600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr1:170132400-170136600	Weak transcription	Left Ventricle	heart
7	chr1:170132400-170136800	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr1:170132400-170140200	Weak transcription	Right Ventricle	heart
9	chr1:170132600-170136800	Weak transcription	Fetal Kidney	kidney
10	chr1:170132600-170136800	Weak transcription	HSMM	muscle
11	chr1:170132600-170137200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr1:170132600-170137200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr1:170132600-170137200	Weak transcription	Osteobl	bone
14	chr1:170132600-170137600	Weak transcription	HSMMtube	muscle
15	chr1:170132800-170140600	Weak transcription	Fetal Heart	heart
16	chr1:170133200-170136800	Weak transcription	NHDF-Ad	bronchial
17	chr1:170135600-170136000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr1:170135800-170136200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr1:170136000-170136800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr1:170136600-170136800	Enhancers	Left Ventricle	heart
21	chr1:170136600-170137000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr1:170136600-170137000	Enhancers	Fetal Stomach	stomach
23	chr1:170136600-170137200	Enhancers	Dnd41	blood
24	chr1:170136600-170137400	Enhancers	Ovary	ovary
25	chr1:170136600-170137600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr1:170136800-170137000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr1:170136800-170137000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:170136800-170137000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr1:170136800-170137000	Enhancers	NHDF-Ad	bronchial
30	chr1:170136800-170137200	Enhancers	Right Atrium	heart
31	chr1:170136800-170137600	Enhancers	Duodenum Smooth Muscle	Duodenum
32	chr1:170136800-170137800	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr1:170136800-170138000	Enhancers	Fetal Kidney	kidney
34	chr1:170136800-170138000	Enhancers	HSMM	muscle
35	chr1:170137000-170137200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr1:170137000-170137400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:170137000-170137400	Enhancers	Hela-S3	cervix
38	chr1:170137000-170137600	Weak transcription	NHDF-Ad	bronchial
39	chr1:170137000-170137800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr1:170137000-170138000	Weak transcription	Fetal Muscle Leg	muscle
41	chr1:170137200-170137400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr1:170137200-170137400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
43	chr1:170137200-170137400	Enhancers	Osteobl	bone
44	chr1:170137200-170137600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:170137200-170138000	Flanking Active TSS	Dnd41	blood
46	chr1:170137200-170138200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr1:170137400-170137800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:170137400-170137800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr1:170137400-170137800	Active TSS	Muscle Satellite Cultured Cells	--
50	chr1:170137400-170137800	Active TSS	Pancreatic Islets	Pancreatic Islet

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