Variant report

Variant	nsv433373
Chromosome Location	chr5:70291250-70649421
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3154)
CpG islands
(count:245)
Chromatin interactive
region (count:0)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:3154 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:70586985-70587016	HepG2	liver:	n/a	n/a
2	BATF	chr5:70536594-70536821	GM12878	blood:	n/a	n/a
3	BATF	chr5:70581590-70581807	GM12878	blood:	n/a	n/a
4	BATF	chr5:70585042-70585622	GM12878	blood:	n/a	n/a
5	BATF	chr5:70473436-70473649	GM12878	blood:	n/a	n/a
6	BATF	chr5:70586369-70587093	GM12878	blood:	n/a	n/a
7	BATF	chr5:70544001-70544158	GM12878	blood:	n/a	n/a
8	BATF	chr5:70538662-70539061	GM12878	blood:	n/a	n/a
9	BATF	chr5:70558118-70558400	GM12878	blood:	n/a	n/a
10	BATF	chr5:70541641-70542422	GM12878	blood:	n/a	n/a
11	BATF	chr5:70456678-70456913	GM12878	blood:	n/a	n/a
12	BATF	chr5:70558503-70558784	GM12878	blood:	n/a	chr5:70558607-70558616
13	BATF	chr5:70555205-70555418	GM12878	blood:	n/a	n/a
14	BATF	chr5:70582281-70582533	GM12878	blood:	n/a	n/a
15	BATF	chr5:70362121-70362600	GM12878	blood:	n/a	n/a
16	BATF	chr5:70523279-70523646	GM12878	blood:	n/a	n/a
17	BATF	chr5:70363439-70363749	GM12878	blood:	n/a	n/a
18	BATF	chr5:70555163-70555361	GM12878	blood:	n/a	n/a
19	BATF	chr5:70600720-70600924	GM12878	blood:	n/a	n/a
20	BATF	chr5:70583052-70583325	GM12878	blood:	n/a	n/a
21	BATF	chr5:70584431-70584744	GM12878	blood:	n/a	n/a
22	BATF	chr5:70575508-70575709	GM12878	blood:	n/a	chr5:70575634-70575644 chr5:70575633-70575644
23	BATF	chr5:70572667-70572911	GM12878	blood:	n/a	n/a
24	BATF	chr5:70616798-70617022	GM12878	blood:	n/a	n/a
25	BATF	chr5:70505333-70505618	GM12878	blood:	n/a	n/a
26	BATF	chr5:70552028-70552325	GM12878	blood:	n/a	n/a
27	BATF	chr5:70581822-70582238	GM12878	blood:	n/a	n/a
28	BATF	chr5:70575917-70576246	GM12878	blood:	n/a	n/a
29	BATF	chr5:70545061-70545287	GM12878	blood:	n/a	n/a
30	BATF	chr5:70578302-70579195	GM12878	blood:	n/a	n/a
31	BATF	chr5:70590285-70590560	GM12878	blood:	n/a	chr5:70590466-70590476
32	BATF	chr5:70574041-70574264	GM12878	blood:	n/a	n/a
33	BATF	chr5:70363259-70363809	GM12878	blood:	n/a	n/a
34	BATF	chr5:70552069-70552305	GM12878	blood:	n/a	n/a
35	BATF	chr5:70598063-70598280	GM12878	blood:	n/a	n/a
36	BATF	chr5:70609718-70609921	GM12878	blood:	n/a	n/a
37	BATF	chr5:70543154-70543357	GM12878	blood:	n/a	n/a
38	BATF	chr5:70582297-70582527	GM12878	blood:	n/a	n/a
39	BATF	chr5:70557586-70557801	GM12878	blood:	n/a	n/a
40	BATF	chr5:70586371-70586849	GM12878	blood:	n/a	n/a
41	BATF	chr5:70557634-70557835	GM12878	blood:	n/a	n/a
42	BATF	chr5:70597986-70598270	GM12878	blood:	n/a	n/a
43	BATF	chr5:70585691-70586274	GM12878	blood:	n/a	n/a
44	BATF	chr5:70558516-70558791	GM12878	blood:	n/a	chr5:70558607-70558616
45	BATF	chr5:70549602-70549824	GM12878	blood:	n/a	n/a
46	BATF	chr5:70543567-70543994	GM12878	blood:	n/a	n/a
47	BATF	chr5:70473270-70473572	GM12878	blood:	n/a	n/a
48	BATF	chr5:70624925-70625151	GM12878	blood:	n/a	n/a
49	BATF	chr5:70582923-70583350	GM12878	blood:	n/a	n/a
50	BATF	chr5:70572459-70572639	GM12878	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:70308497-70308547	Hela-S3	cervix:	n/a
2	chr5:70308497-70308547	Hela-S3	cervix:	n/a
3	chr5:70308497-70308547	HCF	heart:	n/a
4	chr5:70309843-70309893	K562	blood:	n/a
5	chr5:70309843-70309893	AoSMC	blood vessel:	n/a
6	chr5:70309843-70309893	CMK	blood:	n/a
7	chr5:70320693-70320743	A549	lung:	n/a
8	chr5:70308497-70308547	ProgFib	skin:	n/a
9	chr5:70308497-70308547	SKMC	muscle:	n/a
10	chr5:70309843-70309893	NHDF-neo	bronchial:	n/a
11	chr5:70320693-70320743	SAEC	small airway:	n/a
12	chr5:70308497-70308547	PANC-1	pancreas:	n/a
13	chr5:70309843-70309893	A549	lung:	n/a
14	chr5:70308497-70308547	BJ	skin:	n/a
15	chr5:70308497-70308547	HCM	heart:	n/a
16	chr5:70320693-70320743	HMEC	breast:	n/a
17	chr5:70309843-70309893	SAEC	small airway:	n/a
18	chr5:70320693-70320743	MCF10A-Er-Src	breast:	n/a
19	chr5:70309843-70309893	BJ	skin:	n/a
20	chr5:70320693-70320743	NT2-D1	testis:	n/a
21	chr5:70320693-70320743	HRE	kidney:	n/a
22	chr5:70372505-70372555	MCF-7	breast:	n/a
23	chr5:70309843-70309893	H1-hESC	embryonic stem cell:	embryo
24	chr5:70372505-70372555	HAEpiC	amniotic membrane:	n/a
25	chr5:70309843-70309893	AG04450	lung:	fetal
26	chr5:70320693-70320743	SK-N-SH_RA	brain:	n/a
27	chr5:70309843-70309893	GM19239	blood:	n/a
28	chr5:70308497-70308547	HepG2	liver:	n/a
29	chr5:70372505-70372555	Hepatocyte	liver:	n/a
30	chr5:70308497-70308547	ovcar-3	ovarian:	n/a
31	chr5:70308497-70308547	ECC-1	luminal epithelium:	n/a
32	chr5:70309843-70309893	HepG2	liver:	n/a
33	chr5:70308497-70308547	BE2_C	brain:	n/a
34	chr5:70309843-70309893	IMR90	lung:	fetal
35	chr5:70308497-70308547	MCF-7	breast:	n/a
36	chr5:70309843-70309893	MCF-7	breast:	n/a
37	chr5:70309843-70309893	HEEpiC	esophagus:	n/a
38	chr5:70309843-70309893	HRCEpiC	kidney:	n/a
39	chr5:70372505-70372555	T-47D	breast:	n/a
40	chr5:70320693-70320743	HPAEpiC	pulmonary alveolar:	n/a
41	chr5:70372505-70372555	MCF10A-Er-Src	breast:	n/a
42	chr5:70309843-70309893	SK-N-SH	brain:	n/a
43	chr5:70308497-70308547	HRE	kidney:	n/a
44	chr5:70320693-70320743	Jurkat	blood:	n/a
45	chr5:70372505-70372555	GM12892	blood:	n/a
46	chr5:70308497-70308547	GM06990	blood:	n/a
47	chr5:70309843-70309893	SK-N-MC	brain:	n/a
48	chr5:70320693-70320743	CMK	blood:	n/a
49	chr5:70320693-70320743	NB4	blood:	n/a
50	chr5:70372505-70372555	AoSMC	blood vessel:	n/a

No data

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GTF2H2-6	chr5:70528927-70529141	NONHSAT102010
2	lnc-GTF2H2-1	chr5:70328995-70329470	ENSG00000254353
3	lnc-NAIP-1	chr5:70360952-70361049	NONHSAT101997
4	lnc-GTF2H2-3	chr5:70647682-70649750	NONHSAT102012
5	lnc-GTF2H2-7	chr5:70492974-70493188	NONHSAT102005
6	lnc-GTF2H2-7	chr5:70493473-70493608	NONHSAT102005
7	lnc-SMN1-2	chr5:70378669-70379081	NONHSAT101998
8	lnc-GTF2H2-5	chr5:70525720-70525924	NONHSAT102009
9	lnc-BDP1-5	chr5:70504655-70505021	NONHSAT102007
10	lnc-GTF2H2-6	chr5:70529887-70530059	NONHSAT102010
11	lnc-GTF2H2-7	chr5:70493473-70493614	NONHSAT102003
12	lnc-SMN1-3	chr5:70485544-70485865	NONHSAT102004
13	lnc-GTF2H2-7	chr5:70435716-70435861	NONHSAT102003
14	lnc-GTF2H2-3	chr5:70649314-70649750	ENSG00000250387
15	lnc-NAIP-1	chr5:70363123-70363465	NONHSAT101997
16	lnc-GTF2H2-1	chr5:70329997-70330227	ENSG00000254353
17	lnc-GTF2H2-3	chr5:70647682-70649750	ENSG00000250387
18	lnc-GTF2H2-7	chr5:70438472-70438586	NONHSAT102003
19	lnc-NAIP-1	chr5:70358579-70358623	NONHSAT101997

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GTF2H2	hsa-miR-30a-5p	chr5:70331287-70331308

Variant related genes	Relation type
ENSG00000230847	TF binding region
ENSG00000254133	TF binding region
CDH12P4	TF binding region
ENSG00000251634	TF binding region
NAIP	TF binding region
GTF2H2	TF binding region
ENSG00000254353	TF binding region
ENSG00000238451	TF binding region
ENSG00000235558	TF binding region
GUSBP9	TF binding region
ENSG00000254276	TF binding region
ENSG00000230847	CpG island
ENSG00000254133	CpG island
CDH12P4	CpG island
ENSG00000251634	CpG island
NAIP	CpG island
GTF2H2	CpG island
ENSG00000254353	CpG island
ENSG00000238451	CpG island
ENSG00000235558	CpG island
GUSBP9	CpG island
ENSG00000254276	CpG island

Extended variants
information (count: 917 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs207733	chr5:70302824-70302825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs527627190	chr5:70302839-70302840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373135264	chr5:70303128-70303129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533533482	chr5:70303146-70303147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201940132	chr5:70303157-70303158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560838077	chr5:70303470-70303471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570363167	chr5:70303506-70303507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537654423	chr5:70303573-70303574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7714312	chr5:70303679-70303680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549659956	chr5:70303891-70303892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143841352	chr5:70303960-70303961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555903769	chr5:70304054-70304055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567834137	chr5:70304065-70304066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535153129	chr5:70304087-70304088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553518842	chr5:70304274-70304275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571997247	chr5:70304529-70304530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546225661	chr5:70304608-70304609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200364281	chr5:70304646-70304647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201972612	chr5:70304647-70304648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553665890	chr5:70304886-70304887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576768201	chr5:70304904-70304905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs207727	chr5:70304949-70304950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs578183208	chr5:70304966-70304967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544048123	chr5:70305009-70305010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562238837	chr5:70305042-70305043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529435861	chr5:70305070-70305071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541502908	chr5:70305075-70305076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12521267	chr5:70305122-70305123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559531504	chr5:70305138-70305139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555440243	chr5:70305189-70305190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375773676	chr5:70305190-70305191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533360491	chr5:70305201-70305202	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs71612556	chr5:70305205-70305206	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs28394128	chr5:70305206-70305207	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148845991	chr5:70305246-70305247	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545244846	chr5:70305286-70305287	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186419194	chr5:70305305-70305306	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531471366	chr5:70305316-70305317	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549589884	chr5:70305325-70305326	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567894899	chr5:70305340-70305341	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188918371	chr5:70305353-70305354	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs207726	chr5:70305377-70305378	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547465093	chr5:70305393-70305394	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs143512179	chr5:70305415-70305416	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181625967	chr5:70305437-70305438	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186442892	chr5:70305470-70305471	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369643564	chr5:70305471-70305472	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576830790	chr5:70305538-70305539	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs28751879	chr5:70305553-70305554	Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
50	rs542682465	chr5:70305555-70305556	Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:119)

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
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
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
Breast cancer	21785460	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
Medullary thyroid carcinoma	18765511	CNVD
Obesity	21131291	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Autism	21865298	CNVD
Autism	22549408	CNVD
Disease	19212409	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Recurrent pregnancy loss	19789632	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:70302800-70303400	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr5:70303400-70303600	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr5:70303400-70305200	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr5:70303600-70305200	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr5:70303600-70305200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr5:70303600-70305400	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr5:70305200-70308200	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr5:70305200-70308600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr5:70305200-70309600	Strong transcription	Primary neutrophils fromperipheralblood	blood
10	chr5:70305400-70308200	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr5:70305600-70310200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr5:70306400-70309000	Weak transcription	Adipose Nuclei	Adipose
13	chr5:70306400-70309000	Weak transcription	Liver	Liver
14	chr5:70306800-70307000	Enhancers	HepG2	liver
15	chr5:70307000-70307800	Flanking Active TSS	HepG2	liver
16	chr5:70307800-70310000	Enhancers	HepG2	liver
17	chr5:70308200-70309200	Genic enhancers	Primary monocytes fromperipheralblood	blood
18	chr5:70308200-70311000	Genic enhancers	Monocytes-CD14+_RO01746	blood
19	chr5:70308400-70308800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr5:70308600-70310200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr5:70309200-70310000	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr5:70309600-70311000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
23	chr5:70310000-70311200	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr5:70311000-70313600	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr5:70311000-70314000	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr5:70311200-70313200	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr5:70313200-70313800	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr5:70313600-70313800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr5:70313800-70314000	Active TSS	Monocytes-CD14+_RO01746	blood
30	chr5:70314000-70314400	Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr5:70325000-70325400	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr5:70325000-70325400	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr5:70325200-70325600	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr5:70325400-70327600	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr5:70325400-70327800	Weak transcription	Primary neutrophils fromperipheralblood	blood
36	chr5:70325400-70327800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr5:70327600-70328000	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr5:70327800-70328000	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr5:70340200-70351400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr5:70340600-70350600	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr5:70340600-70350600	Weak transcription	Fetal Stomach	stomach
42	chr5:70340800-70350000	Weak transcription	Primary B cells from peripheral blood	blood
43	chr5:70346400-70352000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr5:70346600-70352600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr5:70347600-70352600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr5:70347800-70350800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr5:70348200-70352600	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr5:70348200-70376200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr5:70348400-70350000	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr5:70348400-70350000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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