Variant report

Variant	nsv980979
Chromosome Location	chr5:75561934-75576226
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	BACH1	chr5:75574617-75574623	K562	blood:	n/a	n/a
2	BATF	chr5:75565992-75566373	GM12878	blood:	n/a	chr5:75566211-75566222
3	BATF	chr5:75566023-75566394	GM12878	blood:	n/a	chr5:75566211-75566222
4	BCL3	chr5:75566036-75566403	GM12878	blood:	n/a	chr5:75566182-75566191 chr5:75566215-75566224
5	CEBPB	chr5:75576169-75576376	HepG2	liver:	n/a	n/a
6	CTCF	chr5:75563680-75563830	GM12864	blood:	n/a	n/a
7	CTCF	chr5:75563640-75563790	GM12874	blood:	n/a	n/a
8	CTCF	chr5:75566839-75566865	Lung_OC	lung:	n/a	n/a
9	CTCF	chr5:75563660-75563810	GM12875	blood:	n/a	n/a
10	CTCF	chr5:75563720-75563870	GM12873	blood:	n/a	n/a
11	CTCF	chr5:75569240-75569390	HEEpiC	esophagus:	n/a	n/a
12	CTCF	chr5:75565240-75565390	GM12866	blood:	n/a	n/a
13	CUX1	chr5:75566022-75566265	GM12878	blood:	n/a	n/a
14	EBF1	chr5:75571243-75571561	GM12878	blood:	n/a	chr5:75571375-75571386 chr5:75571378-75571387 chr5:75571376-75571386 chr5:75571375-75571388
15	EBF1	chr5:75571213-75571539	GM12878	blood:	n/a	chr5:75571375-75571386 chr5:75571378-75571387 chr5:75571376-75571386 chr5:75571375-75571388
16	EBF1	chr5:75566066-75566435	GM12878	blood:	n/a	chr5:75566239-75566250
17	EP300	chr5:75567658-75568103	ECC-1	luminal epithelium:	n/a	n/a
18	EP300	chr5:75567529-75568294	ECC-1	luminal epithelium:	n/a	n/a
19	EP300	chr5:75566075-75566334	GM12878	blood:	n/a	chr5:75566111-75566120
20	EP300	chr5:75566057-75566401	GM12878	blood:	n/a	chr5:75566111-75566120
21	ESR1	chr5:75570451-75570763	ECC-1	luminal epithelium:	n/a	n/a
22	ESR1	chr5:75567650-75568121	ECC-1	luminal epithelium:	n/a	n/a
23	ESR1	chr5:75567671-75568050	ECC-1	luminal epithelium:	n/a	n/a
24	ESR1	chr5:75567661-75568128	ECC-1	luminal epithelium:	n/a	n/a
25	ESR1	chr5:75570500-75570740	ECC-1	luminal epithelium:	n/a	n/a
26	ESR1	chr5:75570352-75570755	ECC-1	luminal epithelium:	n/a	n/a
27	FOS	chr5:75566013-75566408	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr5:75566018-75566378	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr5:75566023-75566396	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr5:75566022-75566373	MCF10A-Er-Src	breast:	n/a	n/a
31	GATA2	chr5:75567925-75568340	SH-SY5Y	brain:	n/a	n/a
32	GATA3	chr5:75567944-75568281	MCF-7	breast:	n/a	n/a
33	IRF4	chr5:75566014-75566336	GM12878	blood:	n/a	n/a
34	JUN	chr5:75567136-75567147	HepG2	liver:	n/a	n/a
35	JUN	chr5:75574028-75574049	H1-hESC	embryonic stem cell:	n/a	n/a
36	MAFF	chr5:75569066-75569286	HepG2	liver:	n/a	chr5:75569162-75569180
37	MAFK	chr5:75569041-75569315	HepG2	liver:	n/a	chr5:75569144-75569155 chr5:75569144-75569155 chr5:75569163-75569178
38	MAFK	chr5:75568999-75569284	HepG2	liver:	n/a	chr5:75569144-75569155 chr5:75569144-75569155 chr5:75569163-75569178
39	MAZ	chr5:75565662-75565769	HepG2	liver:	n/a	n/a
40	MYC	chr5:75568449-75568462	H1-hESC	embryonic stem cell:	n/a	n/a
41	NFIC	chr5:75565844-75566405	GM12878	blood:	n/a	n/a
42	NR2F2	chr5:75567662-75568320	MCF-7	breast:	n/a	n/a
43	NR2F2	chr5:75567845-75568212	MCF-7	breast:	n/a	n/a
44	POLR2A	chr5:75565170-75565247	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr5:75569347-75569820	SK-N-MC	brain:	n/a	n/a
46	POU2F2	chr5:75566005-75566509	GM12891	blood:	n/a	chr5:75566307-75566317 chr5:75566307-75566317 chr5:75566316-75566329 chr5:75566308-75566317 chr5:75566316-75566329 chr5:75566309-75566316 chr5:75566304-75566322
47	POU2F2	chr5:75566087-75566445	GM12891	blood:	n/a	chr5:75566307-75566317 chr5:75566307-75566317 chr5:75566316-75566329 chr5:75566308-75566317 chr5:75566316-75566329 chr5:75566309-75566316 chr5:75566304-75566322
48	POU2F2	chr5:75566057-75566500	GM12878	blood:	n/a	chr5:75566307-75566317 chr5:75566307-75566317 chr5:75566316-75566329 chr5:75566308-75566317 chr5:75566316-75566329 chr5:75566309-75566316 chr5:75566304-75566322
49	RAD21	chr5:75567865-75568152	H1-hESC	embryonic stem cell:	n/a	chr5:75568020-75568039 chr5:75568121-75568128
50	RAD21	chr5:75567683-75568211	ECC-1	luminal epithelium:	n/a	chr5:75568020-75568039 chr5:75568121-75568128

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:75564292-75564342	IMR90	lung:	fetal
2	chr5:75564292-75564342	IMR90	lung:	fetal
3	chr5:75564292-75564342	HPAEpiC	pulmonary alveolar:	n/a
4	chr5:75564292-75564342	AG09309	skin:	n/a
5	chr5:75564292-75564342	NB4	blood:	n/a
6	chr5:75564292-75564342	PrEC	prostate:	n/a
7	chr5:75564292-75564342	HCT-116	colon:	n/a
8	chr5:75564292-75564342	SKMC	muscle:	n/a
9	chr5:75564292-75564342	GM19239	blood:	n/a
10	chr5:75564292-75564342	PANC-1	pancreas:	n/a
11	chr5:75564292-75564342	T-47D	breast:	n/a
12	chr5:75564292-75564342	H1-hESC	embryonic stem cell:	embryo
13	chr5:75564292-75564342	HepG2	liver:	n/a
14	chr5:75564292-75564342	SK-N-SH_RA	brain:	n/a
15	chr5:75564292-75564342	HCM	heart:	n/a
16	chr5:75564292-75564342	Hepatocyte	liver:	n/a
17	chr5:75564292-75564342	HNPCEpiC	eye:	n/a
18	chr5:75564292-75564342	HIPEpiC	eye:	n/a
19	chr5:75564292-75564342	GM12891	blood:	n/a
20	chr5:75564292-75564342	HRE	kidney:	n/a
21	chr5:75564292-75564342	NHDF-neo	bronchial:	n/a
22	chr5:75564292-75564342	AG10803	skin:	n/a
23	chr5:75564292-75564342	SK-N-MC	brain:	n/a
24	chr5:75564292-75564342	HRCEpiC	kidney:	n/a
25	chr5:75564292-75564342	SAEC	small airway:	n/a
26	chr5:75564292-75564342	Jurkat	blood:	n/a
27	chr5:75564292-75564342	SK-N-SH	brain:	n/a
28	chr5:75564292-75564342	A549	lung:	n/a
29	chr5:75564292-75564342	BE2_C	brain:	n/a
30	chr5:75564292-75564342	LNCaP	prostate:	n/a
31	chr5:75564292-75564342	HCF	heart:	n/a
32	chr5:75564292-75564342	CMK	blood:	n/a
33	chr5:75564292-75564342	HRPEpiC	eye:	n/a
34	chr5:75564292-75564342	AG04449	skin:	fetal
35	chr5:75564292-75564342	HAEpiC	amniotic membrane:	n/a
36	chr5:75564292-75564342	AoSMC	blood vessel:	n/a
37	chr5:75564292-75564342	PFSK-1	brain:	n/a
38	chr5:75564292-75564342	HCPEpiC	choroid plexus:	n/a
39	chr5:75564292-75564342	GM12892	blood:	n/a
40	chr5:75564292-75564342	GM06990	blood:	n/a
41	chr5:75564292-75564342	MCF10A-Er-Src	breast:	n/a
42	chr5:75564292-75564342	HUVEC	blood vessel:	n/a
43	chr5:75564292-75564342	NH-A	brain:	n/a
44	chr5:75564292-75564342	HEEpiC	esophagus:	n/a
45	chr5:75564292-75564342	RPTEC	kidney:	n/a
46	chr5:75564292-75564342	BJ	skin:	n/a
47	chr5:75564292-75564342	ECC-1	luminal epithelium:	n/a
48	chr5:75564292-75564342	NT2-D1	testis:	n/a
49	chr5:75564292-75564342	HEK293	kidney:	embryo
50	chr5:75564292-75564342	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:75562690..75565535-chr5:75573253..75575190,2	K562	blood:
2	chr5:75562690..75565535-chr5:75573253..75575190,2	K562	blood:
3	chr5:75570576..75572089-chr5:75593353..75595843,2	K562	blood:
4	chr5:75566316..75567948-chr5:75593410..75595007,2	K562	blood:

Variant related genes	Relation type
ENSG00000251107	TF binding region
ENSG00000251107	CpG island

Extended variants
information (count: 588 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:588 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529075048	chr5:75561948-75561949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs34051149	chr5:75561953-75561954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs62361440	chr5:75561965-75561966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549131436	chr5:75562018-75562019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566054991	chr5:75562027-75562028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528543292	chr5:75562053-75562054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148421595	chr5:75562097-75562098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10063681	chr5:75562106-75562107	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs150927249	chr5:75562127-75562128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2937721	chr5:75562129-75562130	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs567592678	chr5:75562134-75562135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536462719	chr5:75562138-75562139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553492812	chr5:75562151-75562152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572052516	chr5:75562173-75562174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369929548	chr5:75562240-75562241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6895220	chr5:75562250-75562251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557511355	chr5:75562292-75562293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143488177	chr5:75562297-75562298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543764954	chr5:75562299-75562300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146744364	chr5:75562331-75562332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543371682	chr5:75562348-75562349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376574694	chr5:75562384-75562385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187993792	chr5:75562389-75562390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2972825	chr5:75562394-75562395	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs6894289	chr5:75562405-75562406	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs542557365	chr5:75562427-75562428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140350286	chr5:75562456-75562457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528623981	chr5:75562475-75562476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs193030129	chr5:75562491-75562492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183026581	chr5:75562505-75562506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530835149	chr5:75562508-75562509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559110990	chr5:75562533-75562534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550528237	chr5:75562575-75562576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2972826	chr5:75562587-75562588	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs150343054	chr5:75562600-75562601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs60469297	chr5:75562615-75562616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546926818	chr5:75562621-75562622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567047891	chr5:75562624-75562625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539748335	chr5:75562625-75562626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs199875687	chr5:75562626-75562627	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534456958	chr5:75562657-75562658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557861301	chr5:75562754-75562755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577782001	chr5:75562758-75562759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537057448	chr5:75562777-75562778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10064140	chr5:75562798-75562799	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs573985721	chr5:75562819-75562820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542903829	chr5:75562906-75562907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187747350	chr5:75562937-75562938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572971970	chr5:75562980-75562981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2972827	chr5:75563073-75563074	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:86)

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
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	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
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	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
Non-small cell lung cancer	21829676	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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:147 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75557200-75574000	Weak transcription	Right Atrium	heart
2	chr5:75562400-75563000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr5:75562400-75563000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr5:75562600-75563200	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr5:75562600-75563200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr5:75563000-75565000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr5:75563000-75566200	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr5:75563200-75563600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr5:75563200-75563600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr5:75563600-75563800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr5:75563600-75564600	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr5:75563800-75564000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr5:75563800-75564200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr5:75563800-75565400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr5:75564000-75564200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:75564200-75565400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr5:75564200-75568000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:75564600-75565000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr5:75565000-75566400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr5:75565000-75566800	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr5:75565200-75566000	Enhancers	Fetal Lung	lung
22	chr5:75565200-75566200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:75565200-75566600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr5:75565200-75566600	Enhancers	Pancreas	Pancrea
25	chr5:75565400-75565600	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr5:75565400-75565600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr5:75565400-75566200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr5:75565400-75566600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr5:75565400-75566600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr5:75565400-75566600	Enhancers	NHEK	skin
31	chr5:75565400-75567000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr5:75565400-75568200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr5:75565400-75569200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr5:75565600-75566000	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr5:75565600-75566200	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr5:75565600-75566200	Enhancers	NH-A	brain
37	chr5:75565600-75566400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr5:75565600-75566600	Enhancers	Primary hematopoietic stem cells	blood
39	chr5:75565600-75566800	Enhancers	GM12878-XiMat	blood
40	chr5:75565800-75566000	Enhancers	Fetal Stomach	stomach
41	chr5:75565800-75566200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr5:75565800-75566400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr5:75565800-75566400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr5:75565800-75566400	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr5:75565800-75566600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr5:75565800-75566600	Enhancers	HMEC	breast
47	chr5:75565800-75568000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr5:75566000-75566200	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr5:75566000-75567800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr5:75566000-75567800	Weak transcription	Fetal Lung	lung

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