Variant report

Variant	nsv1031989
Chromosome Location	chr5:97333291-97524353
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	chr5:97386385-97386732	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr5:97405650-97405889	GM12878	blood:	n/a	chr5:97405750-97405760 chr5:97405746-97405756
3	BCL11A	chr5:97378749-97378960	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr5:97386400-97386600	K562	blood:	n/a	chr5:97386563-97386574
5	CEBPB	chr5:97386405-97386694	MCF-7	breast:	n/a	chr5:97386563-97386574
6	CEBPB	chr5:97386366-97386723	IMR90	lung:	n/a	chr5:97386563-97386574
7	CEBPB	chr5:97394381-97394670	A549	lung:	n/a	chr5:97394544-97394557 chr5:97394544-97394555
8	CEBPB	chr5:97523691-97523908	A549	lung:	n/a	n/a
9	CEBPB	chr5:97441968-97442351	IMR90	lung:	n/a	n/a
10	CEBPB	chr5:97414103-97414348	A549	lung:	n/a	chr5:97414272-97414285 chr5:97414232-97414243
11	CEBPB	chr5:97445423-97446497	IMR90	lung:	n/a	chr5:97446047-97446060 chr5:97446049-97446060 chr5:97446049-97446060 chr5:97446047-97446060
12	CEBPB	chr5:97523617-97523994	IMR90	lung:	n/a	n/a
13	CEBPB	chr5:97378783-97379050	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr5:97386421-97386690	HepG2	liver:	n/a	chr5:97386563-97386574
15	CEBPB	chr5:97431809-97432253	MCF-7	breast:	n/a	chr5:97431999-97432010
16	CEBPB	chr5:97431850-97432122	A549	lung:	n/a	chr5:97431999-97432010
17	CEBPB	chr5:97403393-97403603	A549	lung:	n/a	chr5:97403516-97403527
18	CEBPB	chr5:97397978-97398244	IMR90	lung:	n/a	chr5:97398105-97398116
19	CEBPB	chr5:97335052-97335326	HepG2	liver:	n/a	chr5:97335304-97335315 chr5:97335304-97335313
20	CEBPB	chr5:97462762-97462813	HepG2	liver:	n/a	chr5:97462789-97462800
21	CEBPB	chr5:97398022-97398187	A549	lung:	n/a	chr5:97398105-97398116
22	CEBPB	chr5:97414072-97414411	HepG2	liver:	n/a	chr5:97414272-97414285 chr5:97414232-97414243
23	CEBPB	chr5:97431855-97432188	Hela-S3	cervix:	n/a	chr5:97431999-97432010
24	CEBPB	chr5:97386430-97386669	A549	lung:	n/a	chr5:97386563-97386574
25	CEBPB	chr5:97403339-97403632	IMR90	lung:	n/a	chr5:97403516-97403527
26	CEBPB	chr5:97431799-97432246	IMR90	lung:	n/a	chr5:97431999-97432010
27	CEBPB	chr5:97431846-97432174	H1-hESC	embryonic stem cell:	n/a	chr5:97431999-97432010
28	CEBPB	chr5:97394376-97394700	HepG2	liver:	n/a	chr5:97394544-97394557 chr5:97394544-97394555
29	CEBPB	chr5:97386386-97386756	Hela-S3	cervix:	n/a	chr5:97386563-97386574
30	CEBPB	chr5:97403339-97403649	HepG2	liver:	n/a	chr5:97403516-97403527
31	CEBPB	chr5:97385404-97385851	HepG2	liver:	n/a	chr5:97385748-97385759 chr5:97385748-97385761 chr5:97385748-97385759
32	CEBPB	chr5:97431847-97432186	HepG2	liver:	n/a	chr5:97431999-97432010
33	CEBPB	chr5:97397977-97398256	HepG2	liver:	n/a	chr5:97398105-97398116
34	CHD2	chr5:97386435-97386634	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr5:97493220-97493370	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr5:97447520-97447670	GM12868	blood:	n/a	n/a
37	CTCF	chr5:97447600-97447750	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr5:97493182-97493383	MCF-7	breast:	n/a	n/a
39	CTCF	chr5:97493200-97493350	MCF-7	breast:	n/a	n/a
40	CTCF	chr5:97457380-97457523	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr5:97367240-97367390	GM12868	blood:	n/a	n/a
42	CTCF	chr5:97366120-97366270	HCT-116	colon:	n/a	n/a
43	CTCF	chr5:97366080-97366230	HFF	foreskin:	n/a	n/a
44	CTCF	chr5:97447540-97447690	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr5:97447540-97447690	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr5:97434339-97434379	LNCaP	prostate:	n/a	n/a
47	CTCF	chr5:97366120-97366270	GM12864	blood:	n/a	n/a
48	CTCF	chr5:97366120-97366270	GM12868	blood:	n/a	n/a
49	CTCF	chr5:97457393-97457516	K562	blood:	n/a	n/a
50	CTCF	chr5:97366118-97366267	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:97445281-97445331	HRCEpiC	kidney:	n/a
2	chr5:97445281-97445331	HUVEC	blood vessel:	n/a
3	chr5:97445281-97445331	AoSMC	blood vessel:	n/a
4	chr5:97445281-97445331	ECC-1	luminal epithelium:	n/a
5	chr5:97445281-97445331	T-47D	breast:	n/a
6	chr5:97445281-97445331	NHDF-neo	bronchial:	n/a
7	chr5:97445281-97445331	HepG2	liver:	n/a
8	chr5:97445281-97445331	H1-hESC	embryonic stem cell:	embryo
9	chr5:97445281-97445331	A549	lung:	n/a
10	chr5:97445281-97445331	PANC-1	pancreas:	n/a
11	chr5:97445281-97445331	NB4	blood:	n/a
12	chr5:97445281-97445331	GM12878	blood:	n/a
13	chr5:97445281-97445331	HMEC	breast:	n/a
14	chr5:97445281-97445331	Jurkat	blood:	n/a
15	chr5:97445281-97445331	GM12892	blood:	n/a
16	chr5:97445281-97445331	HRPEpiC	eye:	n/a
17	chr5:97445281-97445331	SKMC	muscle:	n/a
18	chr5:97445281-97445331	GM12891	blood:	n/a
19	chr5:97445281-97445331	PrEC	prostate:	n/a
20	chr5:97445281-97445331	LNCaP	prostate:	n/a
21	chr5:97445281-97445331	Caco-2	colon:	n/a
22	chr5:97445281-97445331	RPTEC	kidney:	n/a
23	chr5:97445281-97445331	SK-N-SH	brain:	n/a
24	chr5:97445281-97445331	Hela-S3	cervix:	n/a
25	chr5:97445281-97445331	MCF10A-Er-Src	breast:	n/a
26	chr5:97445281-97445331	BE2_C	brain:	n/a
27	chr5:97445281-97445331	HEK293	kidney:	embryo
28	chr5:97445281-97445331	SK-N-SH_RA	brain:	n/a
29	chr5:97445281-97445331	ProgFib	skin:	n/a
30	chr5:97445281-97445331	HRE	kidney:	n/a
31	chr5:97445281-97445331	HEEpiC	esophagus:	n/a
32	chr5:97445281-97445331	HIPEpiC	eye:	n/a
33	chr5:97445281-97445331	Hepatocyte	liver:	n/a
34	chr5:97445281-97445331	AG04449	skin:	fetal
35	chr5:97445281-97445331	AG04450	lung:	fetal
36	chr5:97445281-97445331	HPAEpiC	pulmonary alveolar:	n/a
37	chr5:97445281-97445331	NT2-D1	testis:	n/a
38	chr5:97445281-97445331	MCF-7	breast:	n/a
39	chr5:97445281-97445331	HCT-116	colon:	n/a
40	chr5:97445281-97445331	HCF	heart:	n/a
41	chr5:97445281-97445331	HNPCEpiC	eye:	n/a
42	chr5:97445281-97445331	HL-60	blood:	n/a
43	chr5:97445281-97445331	IMR90	lung:	fetal
44	chr5:97445281-97445331	HCM	heart:	n/a
45	chr5:97445281-97445331	SAEC	small airway:	n/a
46	chr5:97445281-97445331	NHBE	bronchial:	n/a
47	chr5:97445281-97445331	SK-N-MC	brain:	n/a
48	chr5:97445281-97445331	BJ	skin:	n/a
49	chr5:97445281-97445331	GM19239	blood:	n/a
50	chr5:97445281-97445331	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:97331985..97334979-chr5:97337146..97339738,2	K562	blood:
2	chr5:97490515..97493248-chr5:97494183..97497100,2	K562	blood:
3	chr5:97331985..97334979-chr5:97337146..97339738,2	K562	blood:
4	chr5:97521008..97523916-chr5:97529057..97531855,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHD1-2	chr5:97421964-97421988	XLOC_004935
2	lnc-CHD1-2	chr5:97496651-97496897	XLOC_004935
3	lnc-CHD1-2	chr5:97496404-97496496	XLOC_004935
4	lnc-CHD1-2	chr5:97496010-97496123	XLOC_004935
5	lnc-CHD1-2	chr5:97429104-97429275	XLOC_004935

Variant related genes	Relation type
ENSG00000248901	TF binding region
ENSG00000249101	TF binding region
ENSG00000248901	CpG island
ENSG00000249101	CpG island
ENSG00000248901	chromatin interactions
ACTR2	miRNA target sites
IKBKE	miRNA target sites
ARFIP1	miRNA target sites
CTLA4	miRNA target sites

Extended variants
information (count: 6971 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:6971 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529034467	chr5:97333295-97333296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs114193599	chr5:97333310-97333311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs72783522	chr5:97333326-97333327	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs533620335	chr5:97333335-97333336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147677003	chr5:97333359-97333360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570396639	chr5:97333385-97333386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570047556	chr5:97333419-97333420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549403214	chr5:97333425-97333426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142332181	chr5:97333438-97333439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs35219834	chr5:97333440-97333441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs257239	chr5:97333442-97333443	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs183376398	chr5:97333455-97333456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553501605	chr5:97333465-97333466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372953835	chr5:97333482-97333483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571928905	chr5:97333541-97333542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187851907	chr5:97333549-97333550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144582304	chr5:97333572-97333573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs17087964	chr5:97333573-97333574	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs147958731	chr5:97333580-97333581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561765497	chr5:97333584-97333585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs372828066	chr5:97333658-97333659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573614531	chr5:97333679-97333680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs72783524	chr5:97333690-97333691	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs72783526	chr5:97333725-97333726	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs533583446	chr5:97333733-97333734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs193177423	chr5:97333737-97333738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549144150	chr5:97333738-97333739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs117075744	chr5:97333753-97333754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531275002	chr5:97333774-97333775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182724424	chr5:97333785-97333786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs72783527	chr5:97333786-97333787	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs73156079	chr5:97333797-97333798	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs370007408	chr5:97333806-97333807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187794261	chr5:97333860-97333861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs370691904	chr5:97333868-97333869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534780112	chr5:97333941-97333942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546702766	chr5:97333954-97333955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571438621	chr5:97333972-97333973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556767653	chr5:97334008-97334009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374371681	chr5:97334019-97334020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs539230517	chr5:97334044-97334045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557581547	chr5:97334051-97334052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7714162	chr5:97334053-97334054	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs537361567	chr5:97334086-97334087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs551307320	chr5:97334094-97334095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555016719	chr5:97334121-97334122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs72783528	chr5:97334167-97334168	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs541094164	chr5:97334183-97334184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533641491	chr5:97334285-97334286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553081406	chr5:97334295-97334296	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	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
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21611746	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97333200-97334600	Enhancers	Fetal Lung	lung
2	chr5:97333400-97335200	Enhancers	Brain Cingulate Gyrus	brain
3	chr5:97333600-97335400	Enhancers	Brain Anterior Caudate	brain
4	chr5:97333600-97336400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr5:97333800-97334600	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr5:97333800-97335600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr5:97333800-97336000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr5:97334000-97334200	Enhancers	Brain Hippocampus Middle	brain
9	chr5:97334000-97334800	Enhancers	Brain Angular Gyrus	brain
10	chr5:97334000-97335200	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr5:97334000-97336000	Enhancers	Brain Substantia Nigra	brain
12	chr5:97334200-97335000	Enhancers	Brain Germinal Matrix	brain
13	chr5:97334400-97335000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr5:97334400-97335200	Weak transcription	Brain Hippocampus Middle	brain
15	chr5:97334600-97335200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr5:97335200-97335400	Enhancers	Brain Hippocampus Middle	brain
17	chr5:97335400-97336000	Weak transcription	Brain Hippocampus Middle	brain
18	chr5:97336200-97336400	Enhancers	Brain Hippocampus Middle	brain
19	chr5:97339800-97340200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
20	chr5:97346600-97350000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr5:97350000-97350400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr5:97350200-97350400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr5:97350200-97350600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr5:97350600-97350800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:97350800-97353200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr5:97352200-97352800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr5:97352600-97352800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr5:97353200-97353600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr5:97353600-97355800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr5:97355800-97356200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:97356400-97358600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:97358200-97367600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr5:97358400-97358800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
34	chr5:97367000-97368600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr5:97367200-97367600	Enhancers	HMEC	breast
36	chr5:97367200-97368000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr5:97367200-97368000	Enhancers	NHEK	skin
38	chr5:97367400-97367800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr5:97367400-97368000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr5:97367600-97368200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr5:97375200-97378000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:97377400-97377800	Enhancers	HUVEC	blood vessel
43	chr5:97377600-97378600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr5:97377600-97379200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr5:97377800-97378400	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr5:97377800-97379200	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr5:97377800-97379400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr5:97377800-97379600	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr5:97378000-97378800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr5:97378000-97379800	Enhancers	HUES48 Cell Line	embryonic stem cell

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