Variant report

Variant	nsv598323
Chromosome Location	chr5:61428137-61461609
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	BRCA1	chr5:61429174-61429235	GM12878	blood:	n/a	n/a
2	CEBPB	chr5:61459905-61460138	K562	blood:	n/a	n/a
3	CEBPB	chr5:61435688-61435816	K562	blood:	n/a	chr5:61435701-61435712
4	CEBPB	chr5:61435638-61435838	HepG2	liver:	n/a	chr5:61435701-61435712
5	CEBPB	chr5:61428083-61428425	Hela-S3	cervix:	n/a	chr5:61428233-61428244 chr5:61428231-61428244
6	CEBPB	chr5:61434610-61434737	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr5:61430860-61431010	AG09309	skin:	n/a	n/a
8	CTCF	chr5:61439580-61439730	GM12872	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
9	CTCF	chr5:61439560-61439710	HCFaa	heart:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
10	CTCF	chr5:61439520-61439670	GM12867	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
11	CTCF	chr5:61439560-61439710	MCF-7	breast:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
12	CTCF	chr5:61439580-61439730	WERI-Rb-1	eye:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
13	CTCF	chr5:61439621-61439764	ProgFib	skin:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
14	CTCF	chr5:61439524-61439779	LNCaP	prostate:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
15	CTCF	chr5:61442440-61442590	GM12865	blood:	n/a	n/a
16	CTCF	chr5:61439473-61439849	IMR90	lung:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
17	CTCF	chr5:61439600-61439750	AoAF	blood vessel:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
18	CTCF	chr5:61439620-61439770	AG09309	skin:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
19	CTCF	chr5:61440180-61440330	AG04449	skin:	n/a	n/a
20	CTCF	chr5:61439458-61439853	GM12878	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
21	CTCF	chr5:61439549-61439762	Pancreas_OC	pancreas:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
22	CTCF	chr5:61439580-61439730	GM12864	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
23	CTCF	chr5:61439200-61439350	Caco-2	colon:	n/a	n/a
24	CTCF	chr5:61439600-61439750	HA-sp	spinal cord:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
25	CTCF	chr5:61439496-61439877	MCF-7	breast:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
26	CTCF	chr5:61439580-61439730	AG09319	gingival:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
27	CTCF	chr5:61440400-61440550	HCFaa	heart:	n/a	n/a
28	CTCF	chr5:61439560-61439710	GM12868	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
29	CTCF	chr5:61439640-61439790	GM12873	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661
30	CTCF	chr5:61439640-61439790	HCT-116	colon:	n/a	chr5:61439644-61439660 chr5:61439643-61439661
31	CTCF	chr5:61440220-61440370	AG09309	skin:	n/a	n/a
32	CTCF	chr5:61439560-61439710	GM12872	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
33	CTCF	chr5:61439660-61439810	HFF	foreskin:	n/a	n/a
34	CTCF	chr5:61439460-61439610	WI-38	lung:	n/a	n/a
35	CTCF	chr5:61433020-61433170	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr5:61439614-61439745	GM20000	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
37	CTCF	chr5:61439393-61439898	MCF-7	breast:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
38	CTCF	chr5:61439478-61439737	K562	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
39	CTCF	chr5:61439228-61440046	A549	lung:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
40	CTCF	chr5:61439620-61439770	GM12865	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
41	CTCF	chr5:61439562-61439790	MCF-7	breast:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
42	CTCF	chr5:61439560-61439710	BE2_C	brain:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
43	CTCF	chr5:61439560-61439710	SAEC	small airway:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
44	CTCF	chr5:61439559-61439758	GM10266	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
45	CTCF	chr5:61439820-61439970	GM12872	blood:	n/a	n/a
46	CTCF	chr5:61439580-61439730	NB4	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
47	CTCF	chr5:61439560-61439710	GM12871	blood:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
48	CTCF	chr5:61439577-61439760	HepG2	liver:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659
49	CTCF	chr5:61454712-61454800	K562	blood:	n/a	n/a
50	CTCF	chr5:61439532-61439832	A549	lung:	n/a	chr5:61439644-61439660 chr5:61439643-61439661 chr5:61439638-61439659

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:61439790-61439840	SK-N-MC	brain:	n/a
2	chr5:61439790-61439840	SK-N-MC	brain:	n/a
3	chr5:61439790-61439840	AG04450	lung:	fetal
4	chr5:61439790-61439840	T-47D	breast:	n/a
5	chr5:61439790-61439840	IMR90	lung:	fetal
6	chr5:61433576-61433626	CMK	blood:	n/a
7	chr5:61433576-61433626	H1-hESC	embryonic stem cell:	embryo
8	chr5:61439790-61439840	Hepatocyte	liver:	n/a
9	chr5:61433576-61433626	PANC-1	pancreas:	n/a
10	chr5:61433576-61433626	HPAEpiC	pulmonary alveolar:	n/a
11	chr5:61439790-61439840	HCF	heart:	n/a
12	chr5:61433576-61433626	Hepatocyte	liver:	n/a
13	chr5:61433576-61433626	HEK293	kidney:	embryo
14	chr5:61433576-61433626	ovcar-3	ovarian:	n/a
15	chr5:61439790-61439840	AG09309	skin:	n/a
16	chr5:61433576-61433626	HCF	heart:	n/a
17	chr5:61439790-61439840	HPAEpiC	pulmonary alveolar:	n/a
18	chr5:61433576-61433626	HAEpiC	amniotic membrane:	n/a
19	chr5:61439790-61439840	BJ	skin:	n/a
20	chr5:61439790-61439840	NT2-D1	testis:	n/a
21	chr5:61439790-61439840	HMEC	breast:	n/a
22	chr5:61439790-61439840	MCF10A-Er-Src	breast:	n/a
23	chr5:61439790-61439840	SK-N-SH_RA	brain:	n/a
24	chr5:61433576-61433626	Hela-S3	cervix:	n/a
25	chr5:61433576-61433626	BJ	skin:	n/a
26	chr5:61439790-61439840	HRPEpiC	eye:	n/a
27	chr5:61433576-61433626	HEEpiC	esophagus:	n/a
28	chr5:61433576-61433626	HepG2	liver:	n/a
29	chr5:61439790-61439840	K562	blood:	n/a
30	chr5:61433576-61433626	HCT-116	colon:	n/a
31	chr5:61433576-61433626	NHDF-neo	bronchial:	n/a
32	chr5:61433576-61433626	AG10803	skin:	n/a
33	chr5:61439790-61439840	MCF-7	breast:	n/a
34	chr5:61433576-61433626	K562	blood:	n/a
35	chr5:61433576-61433626	AG04450	lung:	fetal
36	chr5:61439790-61439840	SK-N-SH	brain:	n/a
37	chr5:61439790-61439840	HRE	kidney:	n/a
38	chr5:61439790-61439840	HL-60	blood:	n/a
39	chr5:61439790-61439840	AG04449	skin:	fetal
40	chr5:61433576-61433626	HNPCEpiC	eye:	n/a
41	chr5:61433576-61433626	ECC-1	luminal epithelium:	n/a
42	chr5:61433576-61433626	NH-A	brain:	n/a
43	chr5:61433576-61433626	SAEC	small airway:	n/a
44	chr5:61439790-61439840	LNCaP	prostate:	n/a
45	chr5:61439790-61439840	A549	lung:	n/a
46	chr5:61439790-61439840	ProgFib	skin:	n/a
47	chr5:61433576-61433626	HRE	kidney:	n/a
48	chr5:61439790-61439840	HUVEC	blood vessel:	n/a
49	chr5:61439790-61439840	Jurkat	blood:	n/a
50	chr5:61439790-61439840	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:61442438..61445370-chr5:61445571..61447544,2	MCF-7	breast:
2	chr5:61437415..61439852-chr5:61446212..61449062,2	K562	blood:
3	chr5:61439485..61439993-chr5:61501806..61502567,2	MCF-7	breast:
4	chr5:61424317..61428011-chr5:61428590..61430862,3	K562	blood:
5	chr5:61426729..61428623-chr5:61433121..61435714,2	K562	blood:
6	chr5:61422681..61424219-chr5:61436524..61438145,2	MCF-7	breast:
7	chr5:61426729..61428623-chr5:61433121..61435714,2	K562	blood:
8	chr5:61437415..61439852-chr5:61446212..61449062,2	K562	blood:
9	chr5:61229619..61230608-chr5:61439489..61440182,2	MCF-7	breast:
10	chr12:125398291..125400539-chr5:61461576..61463918,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF2A-2	chr5:61442492-61442773	NONHSAT101705

Variant related genes	Relation type
RN7SKP157	TF binding region
RN7SKP157	CpG island
ENSG00000265345	chromatin interactions
ENSG00000150991	chromatin interactions
ENSG00000251983	chromatin interactions

Extended variants
information (count: 731 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:731 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1423127	chr5:61428137-61428138	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs75697640	chr5:61428150-61428151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568327803	chr5:61428180-61428181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537457677	chr5:61428208-61428209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs150025687	chr5:61428252-61428253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575973638	chr5:61428257-61428258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184848312	chr5:61428258-61428259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190495109	chr5:61428275-61428276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181802253	chr5:61428278-61428279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540735635	chr5:61428287-61428288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138058867	chr5:61428377-61428378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185125547	chr5:61428396-61428397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189757588	chr5:61428422-61428423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561052313	chr5:61428432-61428433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543450883	chr5:61428482-61428483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563961985	chr5:61428488-61428489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1423128	chr5:61428489-61428490	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs140063149	chr5:61428524-61428525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566174106	chr5:61428543-61428544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181190664	chr5:61428591-61428592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1363785	chr5:61428613-61428614	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs548348800	chr5:61428663-61428664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185185533	chr5:61428671-61428672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544186763	chr5:61428684-61428685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556985031	chr5:61428701-61428702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143609169	chr5:61428716-61428717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538583062	chr5:61428762-61428763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189664663	chr5:61428807-61428808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572121514	chr5:61428862-61428863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs73760563	chr5:61428884-61428885	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs554326621	chr5:61428957-61428958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549643001	chr5:61428976-61428977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368241197	chr5:61428984-61428985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs180727760	chr5:61428995-61428996	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543438817	chr5:61429066-61429067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs146797597	chr5:61429092-61429093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140490383	chr5:61429234-61429235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201152190	chr5:61429249-61429250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546482960	chr5:61429279-61429280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143211140	chr5:61429358-61429359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187309423	chr5:61429366-61429367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568947129	chr5:61429371-61429372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375743291	chr5:61429391-61429392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192105156	chr5:61429461-61429462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183461611	chr5:61429478-61429479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530943655	chr5:61429485-61429486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199996950	chr5:61429509-61429510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550546595	chr5:61429522-61429523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188614817	chr5:61429573-61429574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560840634	chr5:61429588-61429589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:228 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61427400-61428200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr5:61427600-61428800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:61427800-61428200	Enhancers	Osteobl	bone
4	chr5:61427800-61428400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:61427800-61428800	Enhancers	HMEC	breast
6	chr5:61427800-61429000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr5:61428000-61428400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr5:61428200-61429000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr5:61428200-61429200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr5:61428400-61428800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr5:61428800-61429000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:61428800-61430600	Weak transcription	HMEC	breast
13	chr5:61429000-61430400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr5:61429200-61430200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr5:61430400-61430600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr5:61430400-61431000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr5:61430600-61431200	Enhancers	HMEC	breast
18	chr5:61430800-61431200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr5:61432400-61433200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr5:61432600-61432800	Enhancers	H9 Cell Line	embryonic stem cell
21	chr5:61432600-61433200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
22	chr5:61432600-61433400	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr5:61432600-61433600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr5:61432800-61433000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr5:61432800-61433000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr5:61432800-61433000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr5:61432800-61433200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr5:61432800-61433200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr5:61432800-61433200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr5:61432800-61434400	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr5:61433000-61433200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr5:61433000-61433200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr5:61433000-61434200	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr5:61433000-61434400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr5:61433200-61433400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr5:61433200-61434200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr5:61433200-61434200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr5:61433200-61434400	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr5:61433200-61434400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr5:61433200-61434400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:61433200-61434400	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr5:61433200-61434800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr5:61433400-61433800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr5:61433400-61434000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr5:61433600-61434000	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr5:61433800-61435200	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr5:61434000-61434600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr5:61434000-61435200	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr5:61434200-61434800	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr5:61434200-61435200	Enhancers	HUES6 Cell Line	embryonic stem cell

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