Variant report

Variant	nsv881738
Chromosome Location	chr5:62039960-62110910
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	BCL3	chr5:62073699-62074050	GM12878	blood:	n/a	n/a
2	BCL3	chr5:62056284-62056836	GM12878	blood:	n/a	n/a
3	BHLHE40	chr5:62058497-62058551	GM12878	blood:	n/a	n/a
4	BHLHE40	chr5:62072439-62072720	K562	blood:	n/a	n/a
5	CEBPB	chr5:62086239-62086436	HepG2	liver:	n/a	chr5:62086349-62086360
6	CEBPB	chr5:62081416-62081734	K562	blood:	n/a	chr5:62081560-62081571
7	CEBPB	chr5:62069358-62069648	A549	lung:	n/a	chr5:62069514-62069525
8	CEBPB	chr5:62069362-62069624	IMR90	lung:	n/a	chr5:62069514-62069525
9	CEBPB	chr5:62086187-62086537	HepG2	liver:	n/a	chr5:62086349-62086360
10	CEBPB	chr5:62069399-62069579	K562	blood:	n/a	chr5:62069514-62069525
11	CEBPB	chr5:62069352-62069685	HepG2	liver:	n/a	chr5:62069514-62069525
12	CEBPB	chr5:62086290-62086542	K562	blood:	n/a	chr5:62086349-62086360
13	CEBPB	chr5:62086167-62086547	HepG2	liver:	n/a	chr5:62086349-62086360
14	CEBPB	chr5:62086172-62086415	HepG2	liver:	n/a	chr5:62086349-62086360
15	CEBPB	chr5:62069335-62069679	K562	blood:	n/a	chr5:62069514-62069525
16	CEBPB	chr5:62086188-62086582	MCF-7	breast:	n/a	chr5:62086349-62086360
17	CEBPB	chr5:62086159-62086542	Hela-S3	cervix:	n/a	chr5:62086349-62086360
18	CEBPB	chr5:62086162-62086558	MCF-7	breast:	n/a	chr5:62086349-62086360
19	CEBPB	chr5:62086198-62086513	A549	lung:	n/a	chr5:62086349-62086360
20	CEBPB	chr5:62074833-62075055	A549	lung:	n/a	chr5:62074994-62075011
21	CEBPB	chr5:62074801-62075107	Hela-S3	cervix:	n/a	chr5:62074994-62075011
22	CEBPB	chr5:62081409-62081741	HepG2	liver:	n/a	chr5:62081560-62081571
23	CEBPB	chr5:62086170-62086530	IMR90	lung:	n/a	chr5:62086349-62086360
24	CHD2	chr5:62048632-62048830	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr5:62086980-62087130	BE2_C	brain:	n/a	n/a
26	CTCF	chr5:62048720-62049090	A549	lung:	n/a	n/a
27	CTCF	chr5:62074880-62075030	HEK293	kidney:	n/a	chr5:62074961-62074979 chr5:62074962-62074978 chr5:62074956-62074977
28	CTCF	chr5:62074848-62075001	GM12892	blood:	n/a	chr5:62074961-62074979 chr5:62074962-62074978 chr5:62074956-62074977
29	CTCF	chr5:62074818-62075112	K562	blood:	n/a	chr5:62074961-62074979 chr5:62074962-62074978 chr5:62074956-62074977
30	CTCF	chr5:62074735-62075127	HCT-116	colon:	n/a	chr5:62074961-62074979 chr5:62074962-62074978 chr5:62074956-62074977
31	CTCF	chr5:62074860-62075010	GM12872	blood:	n/a	chr5:62074961-62074979 chr5:62074962-62074978 chr5:62074956-62074977
32	CTCF	chr5:62086940-62087090	HFF	foreskin:	n/a	n/a
33	CTCF	chr5:62074880-62075030	HCT-116	colon:	n/a	chr5:62074961-62074979 chr5:62074962-62074978 chr5:62074956-62074977
34	CTCF	chr5:62086980-62087130	BJ	skin:	n/a	n/a
35	CTCF	chr5:62074900-62075050	HepG2	liver:	n/a	chr5:62074961-62074979 chr5:62074962-62074978 chr5:62074956-62074977
36	CTCF	chr5:62087020-62087170	HCFaa	heart:	n/a	n/a
37	CTCF	chr5:62086980-62087130	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr5:62087020-62087170	GM12865	blood:	n/a	n/a
39	CTCF	chr5:62076800-62076950	HRE	kidney:	n/a	n/a
40	CTCF	chr5:62087040-62087190	HCT-116	colon:	n/a	n/a
41	CTCF	chr5:62048922-62049008	GM12892	blood:	n/a	n/a
42	CTCF	chr5:62076880-62077030	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr5:62074608-62075295	HCT-116	colon:	n/a	chr5:62074961-62074979 chr5:62074962-62074978 chr5:62074956-62074977
44	CTCF	chr5:62074828-62075014	GM19238	blood:	n/a	chr5:62074961-62074979 chr5:62074962-62074978 chr5:62074956-62074977
45	CTCF	chr5:62074855-62075073	GM13976	blood:	n/a	chr5:62074961-62074979 chr5:62074962-62074978 chr5:62074956-62074977
46	CTCF	chr5:62086940-62087090	GM12873	blood:	n/a	n/a
47	CTCF	chr5:62048958-62049021	Fibrobl	skin:	n/a	n/a
48	CTCF	chr5:62074860-62075010	GM12878	blood:	n/a	chr5:62074961-62074979 chr5:62074962-62074978 chr5:62074956-62074977
49	CTCF	chr5:62087009-62087153	GM13977	blood:	n/a	n/a
50	CTCF	chr5:62086980-62087130	GM12873	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:62071572-62071622	RPTEC	kidney:	n/a
2	chr5:62073623-62073673	HNPCEpiC	eye:	n/a
3	chr5:62074572-62074622	PrEC	prostate:	n/a
4	chr5:62100540-62100590	RPTEC	kidney:	n/a
5	chr5:62073161-62073211	GM12892	blood:	n/a
6	chr5:62100540-62100590	HCPEpiC	choroid plexus:	n/a
7	chr5:62074261-62074311	CMK	blood:	n/a
8	chr5:62073623-62073673	U87	brain:	n/a
9	chr5:62074261-62074311	U87	brain:	n/a
10	chr5:62074261-62074311	HEEpiC	esophagus:	n/a
11	chr5:62071572-62071622	NH-A	brain:	n/a
12	chr5:62073623-62073673	AG09319	gingival:	n/a
13	chr5:62073623-62073673	BE2_C	brain:	n/a
14	chr5:62072660-62072710	HCPEpiC	choroid plexus:	n/a
15	chr5:62072660-62072710	HRE	kidney:	n/a
16	chr5:62074572-62074622	NHBE	bronchial:	n/a
17	chr5:62071572-62071622	AG09319	gingival:	n/a
18	chr5:62100540-62100590	SK-N-SH	brain:	n/a
19	chr5:62074572-62074622	HAEpiC	amniotic membrane:	n/a
20	chr5:62071572-62071622	AoSMC	blood vessel:	n/a
21	chr5:62071572-62071622	HAEpiC	amniotic membrane:	n/a
22	chr5:62100540-62100590	Hepatocyte	liver:	n/a
23	chr5:62074261-62074311	GM12891	blood:	n/a
24	chr5:62073623-62073673	GM06990	blood:	n/a
25	chr5:62071572-62071622	HRPEpiC	eye:	n/a
26	chr5:62074261-62074311	AoSMC	blood vessel:	n/a
27	chr5:62072660-62072710	HEEpiC	esophagus:	n/a
28	chr5:62073623-62073673	NH-A	brain:	n/a
29	chr5:62074572-62074622	NH-A	brain:	n/a
30	chr5:62072660-62072710	GM12892	blood:	n/a
31	chr5:62071572-62071622	LNCaP	prostate:	n/a
32	chr5:62073623-62073673	HAEpiC	amniotic membrane:	n/a
33	chr5:62074261-62074311	HCPEpiC	choroid plexus:	n/a
34	chr5:62073623-62073673	AG04449	skin:	fetal
35	chr5:62073161-62073211	BJ	skin:	n/a
36	chr5:62100540-62100590	HIPEpiC	eye:	n/a
37	chr5:62072660-62072710	PANC-1	pancreas:	n/a
38	chr5:62073161-62073211	HepG2	liver:	n/a
39	chr5:62072660-62072710	HIPEpiC	eye:	n/a
40	chr5:62100540-62100590	IMR90	lung:	fetal
41	chr5:62100540-62100590	HCM	heart:	n/a
42	chr5:62071572-62071622	SKMC	muscle:	n/a
43	chr5:62073623-62073673	Hela-S3	cervix:	n/a
44	chr5:62100540-62100590	HNPCEpiC	eye:	n/a
45	chr5:62071572-62071622	Jurkat	blood:	n/a
46	chr5:62074572-62074622	IMR90	lung:	fetal
47	chr5:62071572-62071622	HEK293	kidney:	embryo
48	chr5:62100540-62100590	NH-A	brain:	n/a
49	chr5:62071572-62071622	Hepatocyte	liver:	n/a
50	chr5:62072660-62072710	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:62068406..62072262-chr5:62073628..62078748,5	K562	blood:
2	chr5:62071591..62073108-chr5:62074194..62077077,2	K562	blood:
3	chr5:62061013..62063521-chr5:62063661..62066191,2	K562	blood:
4	chr5:61756022..61757748-chr5:62074424..62075807,9	MCF-7	breast:
5	chr5:62078011..62080327-chr5:62081236..62083654,2	K562	blood:
6	chr5:62069461..62071077-chr5:62076501..62078748,2	K562	blood:
7	chr5:62080331..62084292-chr5:62086443..62088883,3	K562	blood:
8	chr5:62061013..62063521-chr5:62063661..62066191,2	K562	blood:
9	chr5:62036443..62039207-chr5:62041195..62044511,3	K562	blood:
10	chr5:62080331..62084292-chr5:62086443..62088883,3	K562	blood:
11	chr5:62069461..62071077-chr5:62076501..62078748,2	K562	blood:
12	chr5:61756416..61757318-chr5:62074341..62075268,4	K562	blood:
13	chr5:62017098..62019061-chr5:62042354..62044460,2	K562	blood:
14	chr5:62078011..62080327-chr5:62081236..62083654,2	K562	blood:
15	chr5:62068406..62072262-chr5:62073628..62078748,5	K562	blood:
16	chr5:62030684..62032945-chr5:62039649..62042488,2	MCF-7	breast:

Variant related genes	Relation type
ISCA1P1	TF binding region
ISCA1P1	CpG island
ENSG00000217416	chromatin interactions

Extended variants
information (count: 893 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16891019	chr5:62039960-62039961	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569753785	chr5:62040008-62040009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs112125989	chr5:62040057-62040058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538769595	chr5:62040061-62040062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs149020829	chr5:62040093-62040094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143418316	chr5:62040094-62040095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34279465	chr5:62040152-62040153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2642770	chr5:62040170-62040171	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs554571951	chr5:62040229-62040230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574437676	chr5:62040260-62040261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571090694	chr5:62040272-62040273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs146873410	chr5:62040279-62040280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186916627	chr5:62040304-62040305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531671084	chr5:62040320-62040321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191367788	chr5:62040335-62040336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545190487	chr5:62040384-62040385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75428464	chr5:62040432-62040433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527887171	chr5:62040499-62040500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35289537	chr5:62040504-62040505	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs567952855	chr5:62040524-62040525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530454180	chr5:62040530-62040531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7717316	chr5:62040545-62040546	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs569693127	chr5:62040578-62040579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111321562	chr5:62040722-62040723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558379327	chr5:62040734-62040735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565821270	chr5:62040747-62040748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534515325	chr5:62040754-62040755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554382371	chr5:62040771-62040772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547435174	chr5:62040807-62040808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11418771	chr5:62040825-62040826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138386619	chr5:62040866-62040867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536976151	chr5:62040923-62040924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541492376	chr5:62040954-62040955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556109623	chr5:62040974-62040975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111341460	chr5:62040993-62040994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7717832	chr5:62040998-62040999	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs565235118	chr5:62041049-62041050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34433761	chr5:62041051-62041052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572546487	chr5:62041059-62041060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373514325	chr5:62041075-62041076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561496127	chr5:62041091-62041092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183284886	chr5:62041130-62041131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550513216	chr5:62041141-62041142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540534381	chr5:62041142-62041143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563234024	chr5:62041155-62041156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538371657	chr5:62041168-62041169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141895999	chr5:62041171-62041172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552198741	chr5:62041189-62041190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565627512	chr5:62041221-62041222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534749574	chr5:62041278-62041279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:62037200-62040000	Enhancers	Fetal Intestine Small	intestine
2	chr5:62038200-62040200	Enhancers	Fetal Intestine Large	intestine
3	chr5:62038400-62040400	Enhancers	HepG2	liver
4	chr5:62039400-62040200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr5:62039600-62040000	Enhancers	Brain Germinal Matrix	brain
6	chr5:62039600-62040400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:62040000-62040400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr5:62040200-62045200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr5:62045200-62045600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr5:62048000-62048600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:62048000-62049200	Active TSS	A549	lung
12	chr5:62048000-62049200	Active TSS	Hela-S3	cervix
13	chr5:62048200-62049000	Active TSS	K562	blood
14	chr5:62048600-62049000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr5:62066600-62067600	Enhancers	Fetal Kidney	kidney
16	chr5:62073800-62074000	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr5:62073800-62074600	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr5:62074000-62074200	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr5:62074000-62074600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr5:62074000-62075000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
21	chr5:62074000-62075400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr5:62074200-62074600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr5:62074200-62074800	Enhancers	Fetal Lung	lung
24	chr5:62074200-62075000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
25	chr5:62074200-62075000	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr5:62074400-62074600	Enhancers	Primary hematopoietic stem cells	blood
27	chr5:62074400-62075000	Enhancers	Primary B cells from cord blood	blood
28	chr5:62074400-62075000	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr5:62074400-62075400	Enhancers	Fetal Kidney	kidney
30	chr5:62074600-62074800	Flanking Active TSS	Primary hematopoietic stem cells	blood
31	chr5:62074600-62075000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
32	chr5:62074600-62075000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr5:62074600-62075000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr5:62074600-62075000	Enhancers	Dnd41	blood
35	chr5:62074800-62075000	Active TSS	Primary hematopoietic stem cells	blood
36	chr5:62074800-62075000	Enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr5:62074800-62075000	Enhancers	Primary T killer memory cells from peripheral blood	blood
38	chr5:62074800-62075400	Enhancers	Brain Hippocampus Middle	brain
39	chr5:62075000-62077800	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr5:62075000-62079000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr5:62075000-62079200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr5:62075000-62079200	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr5:62076200-62076800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr5:62076200-62077000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr5:62077800-62078200	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr5:62078200-62079200	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr5:62078800-62079400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr5:62078800-62079600	Enhancers	GM12878-XiMat	blood
49	chr5:62079000-62079600	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr5:62079200-62079400	Enhancers	Primary neutrophils fromperipheralblood	blood

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