Variant report

Variant	nsv872847
Chromosome Location	chr1:194269455-194368842
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:367)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:194343865-194344032	K562	blood:	n/a	n/a
2	ATF3	chr1:194311963-194312358	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr1:194312059-194312295	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr1:194334363-194334677	HepG2	liver:	n/a	chr1:194334514-194334525
5	CEBPB	chr1:194368782-194369128	HepG2	liver:	n/a	chr1:194368953-194368964 chr1:194368954-194368965 chr1:194368953-194368966 chr1:194368953-194368966 chr1:194368953-194368966
6	CEBPB	chr1:194273767-194273838	A549	lung:	n/a	n/a
7	CEBPB	chr1:194368800-194369138	IMR90	lung:	n/a	chr1:194368953-194368964 chr1:194368954-194368965 chr1:194368953-194368966 chr1:194368953-194368966 chr1:194368953-194368966
8	CEBPB	chr1:194309672-194309782	A549	lung:	n/a	n/a
9	CEBPB	chr1:194368814-194369097	A549	lung:	n/a	chr1:194368953-194368964 chr1:194368954-194368965 chr1:194368953-194368966 chr1:194368953-194368966 chr1:194368953-194368966
10	CEBPB	chr1:194355353-194355553	HepG2	liver:	n/a	chr1:194355445-194355456 chr1:194355444-194355457
11	CEBPB	chr1:194334390-194334657	K562	blood:	n/a	chr1:194334514-194334525
12	CEBPB	chr1:194334367-194334673	IMR90	lung:	n/a	chr1:194334514-194334525
13	CEBPB	chr1:194330573-194330832	K562	blood:	n/a	chr1:194330728-194330739
14	CEBPB	chr1:194330550-194330806	A549	lung:	n/a	chr1:194330728-194330739
15	CEBPB	chr1:194330514-194330873	Hela-S3	cervix:	n/a	chr1:194330728-194330739
16	CEBPB	chr1:194368769-194369099	Hela-S3	cervix:	n/a	chr1:194368953-194368964 chr1:194368954-194368965 chr1:194368953-194368966 chr1:194368953-194368966 chr1:194368953-194368966
17	CEBPB	chr1:194312110-194312319	A549	lung:	n/a	n/a
18	CEBPB	chr1:194330473-194330868	IMR90	lung:	n/a	chr1:194330728-194330739
19	CEBPB	chr1:194330540-194330888	HepG2	liver:	n/a	chr1:194330728-194330739
20	CREB1	chr1:194312007-194312285	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr1:194312120-194312270	GM12873	blood:	n/a	n/a
22	CTCF	chr1:194312120-194312270	HRPEpiC	eye:	n/a	n/a
23	CTCF	chr1:194312080-194312230	HAc	cerebellar:	n/a	n/a
24	CTCF	chr1:194311775-194311829	MCF-7	breast:	n/a	n/a
25	CTCF	chr1:194312032-194312346	HepG2	liver:	n/a	n/a
26	CTCF	chr1:194311790-194311821	MCF-7	breast:	n/a	n/a
27	CTCF	chr1:194312155-194312230	GM10266	blood:	n/a	n/a
28	CTCF	chr1:194312040-194312190	GM12871	blood:	n/a	n/a
29	CTCF	chr1:194312120-194312270	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr1:194312100-194312250	GM12867	blood:	n/a	n/a
31	CTCF	chr1:194312120-194312270	GM12870	blood:	n/a	n/a
32	CTCF	chr1:194312080-194312230	GM12864	blood:	n/a	n/a
33	CTCF	chr1:194312107-194312256	LNCaP	prostate:	n/a	n/a
34	CTCF	chr1:194312070-194312274	A549	lung:	n/a	n/a
35	CTCF	chr1:194312040-194312190	MCF-7	breast:	n/a	n/a
36	CTCF	chr1:194312080-194312230	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr1:194312071-194312288	K562	blood:	n/a	n/a
38	CTCF	chr1:194312120-194312270	GM12878	blood:	n/a	n/a
39	CTCF	chr1:194312180-194312330	GM12801	blood:	n/a	n/a
40	CTCF	chr1:194312080-194312267	A549	lung:	n/a	n/a
41	CTCF	chr1:194312140-194312290	BE2_C	brain:	n/a	n/a
42	CTCF	chr1:194311993-194312349	GM12878	blood:	n/a	n/a
43	CTCF	chr1:194312103-194312271	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr1:194312046-194312292	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:194311913-194312285	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr1:194311954-194312324	K562	blood:	n/a	n/a
47	CTCF	chr1:194318100-194318250	GM12868	blood:	n/a	n/a
48	CTCF	chr1:194312082-194312280	GM12892	blood:	n/a	n/a
49	CTCF	chr1:194311820-194311970	GM12867	blood:	n/a	n/a
50	CTCF	chr1:194311895-194312367	HCT-116	colon:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:194327715-194327765	GM06990	blood:	n/a
2	chr1:194327715-194327765	HepG2	liver:	n/a
3	chr1:194327715-194327765	BE2_C	brain:	n/a
4	chr1:194327715-194327765	ovcar-3	ovarian:	n/a
5	chr1:194327715-194327765	HNPCEpiC	eye:	n/a
6	chr1:194327715-194327765	SK-N-SH	brain:	n/a
7	chr1:194327715-194327765	A549	lung:	n/a
8	chr1:194327715-194327765	PrEC	prostate:	n/a
9	chr1:194327715-194327765	HCM	heart:	n/a
10	chr1:194327715-194327765	HCT-116	colon:	n/a
11	chr1:194327715-194327765	NB4	blood:	n/a
12	chr1:194327715-194327765	NHBE	bronchial:	n/a
13	chr1:194327715-194327765	NHDF-neo	bronchial:	n/a
14	chr1:194327715-194327765	HRCEpiC	kidney:	n/a
15	chr1:194327715-194327765	BJ	skin:	n/a
16	chr1:194327715-194327765	SAEC	small airway:	n/a
17	chr1:194327715-194327765	Hepatocyte	liver:	n/a
18	chr1:194327715-194327765	GM12891	blood:	n/a
19	chr1:194327715-194327765	AG09309	skin:	n/a
20	chr1:194327715-194327765	T-47D	breast:	n/a
21	chr1:194327715-194327765	IMR90	lung:	fetal
22	chr1:194327715-194327765	LNCaP	prostate:	n/a
23	chr1:194327715-194327765	AG10803	skin:	n/a
24	chr1:194327715-194327765	HCPEpiC	choroid plexus:	n/a
25	chr1:194327715-194327765	HAEpiC	amniotic membrane:	n/a
26	chr1:194327715-194327765	NT2-D1	testis:	n/a
27	chr1:194327715-194327765	RPTEC	kidney:	n/a
28	chr1:194327715-194327765	HEK293	kidney:	embryo
29	chr1:194327715-194327765	HCF	heart:	n/a
30	chr1:194327715-194327765	HIPEpiC	eye:	n/a
31	chr1:194327715-194327765	H1-hESC	embryonic stem cell:	embryo
32	chr1:194327715-194327765	Jurkat	blood:	n/a
33	chr1:194327715-194327765	ECC-1	luminal epithelium:	n/a
34	chr1:194327715-194327765	CMK	blood:	n/a
35	chr1:194327715-194327765	GM12892	blood:	n/a
36	chr1:194327715-194327765	HL-60	blood:	n/a
37	chr1:194327715-194327765	AG04449	skin:	fetal
38	chr1:194327715-194327765	MCF10A-Er-Src	breast:	n/a
39	chr1:194327715-194327765	HRE	kidney:	n/a
40	chr1:194327715-194327765	HMEC	breast:	n/a
41	chr1:194327715-194327765	K562	blood:	n/a
42	chr1:194327715-194327765	PANC-1	pancreas:	n/a
43	chr1:194327715-194327765	AoSMC	blood vessel:	n/a
44	chr1:194327715-194327765	HUVEC	blood vessel:	n/a
45	chr1:194327715-194327765	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:194327715-194327765	PFSK-1	brain:	n/a
47	chr1:194327715-194327765	Hela-S3	cervix:	n/a
48	chr1:194327715-194327765	SK-N-SH_RA	brain:	n/a
49	chr1:194327715-194327765	NH-A	brain:	n/a
50	chr1:194327715-194327765	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:194307530..194310929-chr1:194324369..194327548,3	K562	blood:
2	chr1:194326093..194330986-chr1:194331715..194336171,7	K562	blood:
3	chr1:194290793..194293350-chr1:194303671..194305841,2	K562	blood:
4	chr1:194272409..194275339-chr1:194275984..194279040,4	K562	blood:
5	chr1:194325391..194328027-chr1:194331850..194333464,2	K562	blood:
6	chr1:194326093..194330986-chr1:194331715..194336171,7	K562	blood:
7	chr1:194328262..194330986-chr1:194334081..194336171,2	K562	blood:
8	chr1:194315945..194318461-chr1:194337918..194339837,2	K562	blood:
9	chr1:194286927..194289015-chr1:194296923..194299296,2	K562	blood:
10	chr1:194306516..194309030-chr1:194325392..194327548,2	K562	blood:
11	chr1:194315945..194318461-chr1:194337918..194339837,2	K562	blood:
12	chr1:194308962..194311330-chr4:127715408..127718280,2	MCF-7	breast:
13	chr1:194328262..194330986-chr1:194334081..194336171,2	K562	blood:
14	chr1:194266672..194269041-chr1:194271611..194273227,2	K562	blood:
15	chr1:194307530..194310929-chr1:194324369..194327548,3	K562	blood:
16	chr1:194286927..194289015-chr1:194296923..194299296,2	K562	blood:
17	chr1:193587120..193589760-chr1:194326578..194328851,2	K562	blood:
18	chr1:194290793..194293350-chr1:194303671..194305841,2	K562	blood:
19	chr1:194315164..194317998-chr1:194319254..194321893,3	K562	blood:
20	chr1:194277312..194279906-chr1:194286603..194288414,2	K562	blood:
21	chr1:194320848..194323111-chr1:194332698..194335480,2	K562	blood:
22	chr1:194272409..194275339-chr1:194275984..194279040,4	K562	blood:
23	chr1:194277312..194279906-chr1:194286603..194288414,2	K562	blood:
24	chr1:194325391..194328027-chr1:194331850..194333464,2	K562	blood:
25	chr1:194317795..194320009-chr1:194323102..194324851,2	K562	blood:
26	chr1:194070430..194072677-chr1:194322592..194324190,2	K562	blood:
27	chr1:194306516..194309030-chr1:194325392..194327548,2	K562	blood:
28	chr1:194317795..194320009-chr1:194323102..194324851,2	K562	blood:
29	chr1:194320848..194323111-chr1:194332698..194335480,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-B3GALT2-5	chr1:194280749-194281292	NONHSAT008580
2	lnc-B3GALT2-5	chr1:194296750-194296826	NONHSAT008580
3	lnc-CDC73-4	chr1:194320073-194320368	XLOC_000510
4	lnc-CDC73-4	chr1:194320009-194320481	NONHSAT008581
5	lnc-CDC73-4	chr1:194320593-194321556	NONHSAT008581
6	lnc-CDC73-4	chr1:194321413-194321556	XLOC_000510

No data

Variant related genes	Relation type
ENSG00000231714	TF binding region
ENSG00000231714	CpG island
ENSG00000231714	chromatin interactions

Extended variants
information (count: 1117 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1117 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1018626	chr1:194269455-194269456	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576826526	chr1:194269462-194269463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185871943	chr1:194269493-194269494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537813662	chr1:194269505-194269506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12753448	chr1:194269551-194269552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188287650	chr1:194269561-194269562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs577626111	chr1:194269562-194269563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs193186858	chr1:194269644-194269645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560085998	chr1:194269659-194269660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs958954	chr1:194269842-194269843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs571936975	chr1:194269856-194269857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368106544	chr1:194269862-194269863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs200753920	chr1:194269889-194269890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs16836642	chr1:194269893-194269894	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs572418115	chr1:194269973-194269974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs570068855	chr1:194269982-194269983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370054017	chr1:194269984-194269985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536223265	chr1:194270026-194270027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150343441	chr1:194270035-194270036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184587340	chr1:194270087-194270088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs114894128	chr1:194270090-194270091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188556053	chr1:194270107-194270108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532499168	chr1:194270158-194270159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563396269	chr1:194270224-194270225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566129243	chr1:194270229-194270230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536810929	chr1:194270257-194270258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548823480	chr1:194270274-194270275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570316733	chr1:194270299-194270300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537752110	chr1:194270318-194270319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555877940	chr1:194270329-194270330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs77949240	chr1:194270356-194270357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563767982	chr1:194278640-194278641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531230189	chr1:194278656-194278657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs13373891	chr1:194278691-194278692	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs1325428	chr1:194278715-194278716	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs531946899	chr1:194278719-194278720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139947716	chr1:194278742-194278743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1325427	chr1:194278743-194278744	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs145353307	chr1:194278756-194278757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147235319	chr1:194278780-194278781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181299485	chr1:194278841-194278842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs186037463	chr1:194278844-194278845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs140706831	chr1:194278848-194278849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190901180	chr1:194278894-194278895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1325426	chr1:194278945-194278946	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs553414090	chr1:194278962-194278963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555504378	chr1:194278974-194278975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149970075	chr1:194278977-194278978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs75533515	chr1:194279007-194279008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs183327114	chr1:194279105-194279106	Enhancers	n/a	n/a	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
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	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
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	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
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:194268400-194270000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr1:194269400-194270400	Enhancers	HUVEC	blood vessel
3	chr1:194270000-194270400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:194270000-194270400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:194278600-194279200	Enhancers	A549	lung
6	chr1:194300200-194300600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
7	chr1:194300200-194300600	Active TSS	Breast Myoepithelial Primary Cells	Breast
8	chr1:194307200-194308000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:194307400-194307800	Enhancers	Brain Hippocampus Middle	brain
10	chr1:194307400-194307800	Enhancers	Brain Substantia Nigra	brain
11	chr1:194307400-194308000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:194307400-194308200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:194308600-194309000	Enhancers	Fetal Brain Female	brain
14	chr1:194311600-194311800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr1:194311600-194311800	Active TSS	iPS-15b Cell Line	embryonic stem cell
16	chr1:194311600-194312000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr1:194311600-194312200	Enhancers	H1 Cell Line	embryonic stem cell
18	chr1:194311800-194312000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
19	chr1:194311800-194312000	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr1:194311800-194312200	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr1:194311800-194312200	Enhancers	H9 Cell Line	embryonic stem cell
22	chr1:194311800-194312200	Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr1:194312000-194312200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr1:194315600-194316600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:194316200-194316800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr1:194316400-194316600	Enhancers	Fetal Heart	heart
27	chr1:194316400-194317000	Enhancers	HMEC	breast
28	chr1:194325000-194325200	ZNF genes & repeats	Right Atrium	heart
29	chr1:194325200-194327000	Active TSS	K562	blood
30	chr1:194325200-194329000	Weak transcription	Right Atrium	heart
31	chr1:194327400-194327800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr1:194330400-194332400	Enhancers	Fetal Heart	heart
33	chr1:194335400-194336000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:194335400-194336200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr1:194335600-194339200	Enhancers	HMEC	breast
36	chr1:194336000-194336400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr1:194336000-194336800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr1:194336200-194336600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr1:194336400-194336800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr1:194336800-194338200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:194338000-194338200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:194338200-194338800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr1:194340600-194340800	Enhancers	Brain Hippocampus Middle	brain
44	chr1:194341400-194342000	Enhancers	Brain Substantia Nigra	brain
45	chr1:194341800-194342200	Enhancers	Brain Cingulate Gyrus	brain
46	chr1:194342000-194342200	Enhancers	Brain Hippocampus Middle	brain
47	chr1:194347400-194347600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr1:194363200-194365000	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr1:194363200-194365000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr1:194363200-194365800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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