Variant report

Variant	esv1807344
Chromosome Location	chr5:68849631-68911161
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:662)
CpG islands
(count:611)
Chromatin interactive
region (count:0)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:662 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:68856265-68856477	GM12878	blood:	n/a	n/a
2	BATF	chr5:68897794-68898185	GM12878	blood:	n/a	n/a
3	BATF	chr5:68897780-68898118	GM12878	blood:	n/a	n/a
4	BATF	chr5:68855769-68856236	GM12878	blood:	n/a	n/a
5	BATF	chr5:68856954-68857395	GM12878	blood:	n/a	n/a
6	BATF	chr5:68857142-68857346	GM12878	blood:	n/a	n/a
7	BATF	chr5:68855731-68856077	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:68897742-68898263	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:68855639-68856223	GM12878	blood:	n/a	chr5:68855979-68855988
10	BCL11A	chr5:68897862-68898148	GM12878	blood:	n/a	n/a
11	BCL11A	chr5:68857029-68857406	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:68855749-68856242	GM12878	blood:	n/a	chr5:68855979-68855988
13	BCLAF1	chr5:68855724-68856135	GM12878	blood:	n/a	chr5:68855979-68855988
14	BCLAF1	chr5:68855724-68856116	K562	blood:	n/a	chr5:68855979-68855988
15	BCLAF1	chr5:68855724-68856111	K562	blood:	n/a	chr5:68855979-68855988
16	BCLAF1	chr5:68855732-68856164	GM12878	blood:	n/a	chr5:68855979-68855988
17	BHLHE40	chr5:68855820-68856132	HepG2	liver:	n/a	chr5:68855927-68855943 chr5:68855911-68855927
18	BRCA1	chr5:68855848-68856045	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr5:68855493-68856354	K562	blood:	n/a	n/a
20	CBX3	chr5:68855601-68856119	K562	blood:	n/a	n/a
21	CEBPB	chr5:68855845-68856045	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr5:68857201-68857397	K562	blood:	n/a	n/a
23	CEBPB	chr5:68857055-68857464	K562	blood:	n/a	n/a
24	CEBPD	chr5:68855760-68856284	K562	blood:	n/a	n/a
25	CHD2	chr5:68855923-68856048	GM12878	blood:	n/a	n/a
26	CHD2	chr5:68855844-68855949	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr5:68855853-68856047	Hela-S3	cervix:	n/a	n/a
28	CREB1	chr5:68855831-68856118	A549	lung:	n/a	n/a
29	CTCF	chr5:68855720-68855870	SAEC	small airway:	n/a	n/a
30	CTCF	chr5:68855980-68856130	BJ	skin:	n/a	n/a
31	CTCF	chr5:68855840-68856054	K562	blood:	n/a	n/a
32	CTCF	chr5:68855960-68856110	HPF	lung:	n/a	n/a
33	CTCF	chr5:68855720-68855870	HMF	breast:	n/a	n/a
34	CTCF	chr5:68855854-68855949	MCF-7	breast:	n/a	n/a
35	CTCF	chr5:68855720-68855870	GM12867	blood:	n/a	n/a
36	CTCF	chr5:68855820-68856135	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr5:68855980-68856130	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr5:68855740-68855890	BE2_C	brain:	n/a	n/a
39	CTCF	chr5:68855827-68856045	Medullo	brain:	n/a	n/a
40	CTCF	chr5:68856020-68856170	WI-38	lung:	n/a	n/a
41	CTCF	chr5:68855682-68856139	K562	blood:	n/a	n/a
42	CTCF	chr5:68855700-68855850	HFF	foreskin:	n/a	n/a
43	CTCF	chr5:68855880-68856030	AG04449	skin:	n/a	n/a
44	CTCF	chr5:68855681-68856283	K562	blood:	n/a	n/a
45	CTCF	chr5:68855692-68856174	A549	lung:	n/a	n/a
46	CTCF	chr5:68855816-68856087	GM13976	blood:	n/a	n/a
47	CTCF	chr5:68855700-68855850	GM12870	blood:	n/a	n/a
48	CTCF	chr5:68855831-68856130	GM12878	blood:	n/a	n/a
49	CTCF	chr5:68883919-68883967	Medullo	brain:	n/a	n/a
50	CTCF	chr5:68855980-68856130	Caco-2	colon:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:68856062-68856112	CMK	blood:	n/a
2	chr5:68856062-68856112	CMK	blood:	n/a
3	chr5:68859882-68859932	T-47D	breast:	n/a
4	chr5:68859882-68859932	HAEpiC	amniotic membrane:	n/a
5	chr5:68855560-68855610	GM12892	blood:	n/a
6	chr5:68855560-68855610	NB4	blood:	n/a
7	chr5:68859882-68859932	NH-A	brain:	n/a
8	chr5:68855810-68855860	LNCaP	prostate:	n/a
9	chr5:68855873-68855923	AoSMC	blood vessel:	n/a
10	chr5:68859882-68859932	CMK	blood:	n/a
11	chr5:68855873-68855923	U87	brain:	n/a
12	chr5:68855873-68855923	AG09309	skin:	n/a
13	chr5:68868293-68868343	Caco-2	colon:	n/a
14	chr5:68855873-68855923	AG09319	gingival:	n/a
15	chr5:68857760-68857810	NHDF-neo	bronchial:	n/a
16	chr5:68856077-68856127	HepG2	liver:	n/a
17	chr5:68855810-68855860	GM06990	blood:	n/a
18	chr5:68856077-68856127	AG04450	lung:	fetal
19	chr5:68852996-68853046	A549	lung:	n/a
20	chr5:68856077-68856127	HRCEpiC	kidney:	n/a
21	chr5:68859882-68859932	GM12891	blood:	n/a
22	chr5:68855873-68855923	RPTEC	kidney:	n/a
23	chr5:68855810-68855860	HCPEpiC	choroid plexus:	n/a
24	chr5:68868293-68868343	HIPEpiC	eye:	n/a
25	chr5:68859882-68859932	HIPEpiC	eye:	n/a
26	chr5:68855560-68855610	Caco-2	colon:	n/a
27	chr5:68856077-68856127	HCM	heart:	n/a
28	chr5:68857760-68857810	BE2_C	brain:	n/a
29	chr5:68856062-68856112	HRPEpiC	eye:	n/a
30	chr5:68868293-68868343	Jurkat	blood:	n/a
31	chr5:68855873-68855923	HPAEpiC	pulmonary alveolar:	n/a
32	chr5:68852996-68853046	HCM	heart:	n/a
33	chr5:68857760-68857810	SK-N-MC	brain:	n/a
34	chr5:68855560-68855610	HNPCEpiC	eye:	n/a
35	chr5:68855810-68855860	NH-A	brain:	n/a
36	chr5:68856077-68856127	SK-N-MC	brain:	n/a
37	chr5:68852996-68853046	NT2-D1	testis:	n/a
38	chr5:68856062-68856112	AG09309	skin:	n/a
39	chr5:68855560-68855610	MCF-7	breast:	n/a
40	chr5:68855810-68855860	GM12891	blood:	n/a
41	chr5:68855560-68855610	ECC-1	luminal epithelium:	n/a
42	chr5:68855560-68855610	SK-N-SH	brain:	n/a
43	chr5:68855873-68855923	H1-hESC	embryonic stem cell:	embryo
44	chr5:68857760-68857810	AG04449	skin:	fetal
45	chr5:68856065-68856115	HCPEpiC	choroid plexus:	n/a
46	chr5:68855873-68855923	HepG2	liver:	n/a
47	chr5:68868293-68868343	GM06990	blood:	n/a
48	chr5:68859882-68859932	SAEC	small airway:	n/a
49	chr5:68855873-68855923	HAEpiC	amniotic membrane:	n/a
50	chr5:68855873-68855923	PANC-1	pancreas:	n/a

No data

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GTF2H2C-1	chr5:68889300-68889532	NONHSAT101931
2	lnc-OCLN-1	chr5:68860927-68860960	NONHSAT101929
3	lnc-GTF2H2C-1	chr5:68890071-68890550	NONHSAT101931
4	lnc-OCLN-1	chr5:68856086-68856428	NONHSAT101929
5	lnc-OCLN-1	chr5:68858500-68858597	NONHSAT101929

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GTF2H2D	hsa-miR-30a-5p	chr5:68888221-68888242

Variant related genes	Relation type
ENSG00000248477	TF binding region
GTF2H2C	TF binding region
ENSG00000248477	CpG island
GTF2H2C	CpG island

Extended variants
information (count: 406 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:406 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76080549	chr5:68849631-68849632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551652799	chr5:68849659-68849660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201056955	chr5:68849806-68849807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371132365	chr5:68849929-68849930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548752839	chr5:68850049-68850050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567053400	chr5:68850194-68850195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534412736	chr5:68850195-68850196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187688506	chr5:68850198-68850199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192491213	chr5:68850408-68850409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571231854	chr5:68850459-68850460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535790851	chr5:68850485-68850486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544401846	chr5:68850570-68850571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557658202	chr5:68850572-68850573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575815986	chr5:68850595-68850596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370879112	chr5:68850783-68850784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374446243	chr5:68850784-68850785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185678833	chr5:68850785-68850786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368766545	chr5:68850787-68850788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34202353	chr5:68850788-68850789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371435086	chr5:68850823-68850824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555197700	chr5:68850867-68850868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555987017	chr5:68850870-68850871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs76123058	chr5:68850922-68850923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146986409	chr5:68850963-68850964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565328546	chr5:68850966-68850967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577186893	chr5:68850996-68850997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373178468	chr5:68851064-68851065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371306264	chr5:68851086-68851087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374793047	chr5:68851088-68851089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556647974	chr5:68851207-68851208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574822864	chr5:68851208-68851209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542289114	chr5:68851239-68851240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs62371757	chr5:68851256-68851257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188890364	chr5:68851288-68851289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2666598	chr5:68851297-68851298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192095324	chr5:68851344-68851345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375565190	chr5:68851387-68851388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548814949	chr5:68851391-68851392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2666597	chr5:68851420-68851421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560742776	chr5:68851486-68851487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs256925	chr5:68851541-68851542	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
42	rs184412724	chr5:68851563-68851564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546293974	chr5:68852482-68852483	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs200157655	chr5:68852534-68852535	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs699901	chr5:68853030-68853031	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs189167216	chr5:68853171-68853172	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs538645548	chr5:68853174-68853175	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs77392451	chr5:68853486-68853487	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs200773462	chr5:68853877-68853878	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs550284091	chr5:68853898-68853899	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian cancer	21781307	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
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
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
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
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
abnormal development	18461090	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21990379	CNVD
Hirschsprung''s Disease	21712996	CNVD
Apoptosis	19488400	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Acute monocytic leukemia	16498392	CNVD
Colorectal cancer	20459617	CNVD
Gastric adenocarcinoma	19115996	CNVD
Spinal muscular atrophy	17160897	CNVD
Spinal muscular atrophy	17668391	CNVD
Spinal muscular atrophy	17668395	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pseudo-TORCH syndrome	20727516	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Obesity	21131291	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:341 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68824000-68855400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr5:68829600-68855400	Weak transcription	Fetal Intestine Small	intestine
3	chr5:68841000-68855200	Weak transcription	HepG2	liver
4	chr5:68844400-68855400	Weak transcription	Fetal Intestine Large	intestine
5	chr5:68845800-68855600	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr5:68855000-68855200	Enhancers	Dnd41	blood
7	chr5:68855000-68855600	Enhancers	Primary T cells fromperipheralblood	blood
8	chr5:68855200-68855400	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr5:68855200-68855400	Enhancers	Adipose Nuclei	Adipose
10	chr5:68855200-68855400	Enhancers	Liver	Liver
11	chr5:68855200-68855400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
12	chr5:68855200-68855400	Enhancers	HepG2	liver
13	chr5:68855200-68855400	Enhancers	HUVEC	blood vessel
14	chr5:68855200-68855600	Enhancers	Right Atrium	heart
15	chr5:68855200-68855600	Flanking Active TSS	Dnd41	blood
16	chr5:68855200-68855800	Enhancers	Fetal Brain Male	brain
17	chr5:68855200-68856800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr5:68855200-68857000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:68855400-68855600	Enhancers	Primary B cells from peripheral blood	blood
20	chr5:68855400-68855600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr5:68855400-68855600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr5:68855400-68855600	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr5:68855400-68855600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr5:68855400-68855600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr5:68855400-68855600	Enhancers	Muscle Satellite Cultured Cells	--
26	chr5:68855400-68855600	Enhancers	Fetal Intestine Large	intestine
27	chr5:68855400-68855600	Enhancers	Fetal Muscle Trunk	muscle
28	chr5:68855400-68855600	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr5:68855400-68855600	Flanking Active TSS	HepG2	liver
30	chr5:68855400-68855600	Enhancers	HMEC	breast
31	chr5:68855400-68855600	Enhancers	NHEK	skin
32	chr5:68855400-68855800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
33	chr5:68855400-68855800	Active TSS	Primary T killer memory cells from peripheral blood	blood
34	chr5:68855400-68855800	Flanking Active TSS	Adipose Nuclei	Adipose
35	chr5:68855400-68855800	Flanking Active TSS	Liver	Liver
36	chr5:68855400-68855800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
37	chr5:68855400-68855800	Flanking Active TSS	HUVEC	blood vessel
38	chr5:68855400-68856200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr5:68855400-68856200	Active TSS	Primary T helper naive cells from peripheral blood	blood
40	chr5:68855400-68856600	Active TSS	Primary neutrophils fromperipheralblood	blood
41	chr5:68855400-68856600	Active TSS	Primary B cells from cord blood	blood
42	chr5:68855400-68856600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
43	chr5:68855400-68856800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr5:68855400-68856800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr5:68855400-68856800	Active TSS	Primary T cells from cord blood	blood
46	chr5:68855400-68856800	Active TSS	Primary hematopoietic stem cells short term culture	blood
47	chr5:68855400-68856800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr5:68855400-68856800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr5:68855400-68856800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr5:68855400-68856800	Active TSS	Brain Cingulate Gyrus	brain

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