Variant report

Variant	nsv1034382
Chromosome Location	chr5:105790508-106006157
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	ATF1	chr5:105859633-105859780	K562	blood:	n/a	n/a
2	ATF2	chr5:105937147-105937733	GM12878	blood:	n/a	n/a
3	BATF	chr5:105952746-105952947	GM12878	blood:	n/a	n/a
4	BATF	chr5:105889076-105889285	GM12878	blood:	n/a	n/a
5	BATF	chr5:105889044-105889346	GM12878	blood:	n/a	n/a
6	BATF	chr5:105952737-105952935	GM12878	blood:	n/a	n/a
7	BATF	chr5:105871246-105871400	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:105871234-105871399	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:105889001-105889386	GM12878	blood:	n/a	n/a
10	BHLHE40	chr5:105889035-105889258	HepG2	liver:	n/a	n/a
11	BHLHE40	chr5:105937145-105937565	GM12878	blood:	n/a	n/a
12	BHLHE40	chr5:105938056-105938340	GM12878	blood:	n/a	n/a
13	BHLHE40	chr5:105887552-105887806	GM12878	blood:	n/a	n/a
14	BRCA1	chr5:105871319-105871346	GM12878	blood:	n/a	n/a
15	CBX3	chr5:105790354-105791158	HCT-116	colon:	n/a	n/a
16	CEBPB	chr5:105859111-105859411	HepG2	liver:	n/a	chr5:105859114-105859125 chr5:105859284-105859295
17	CEBPB	chr5:105891864-105892159	IMR90	lung:	n/a	n/a
18	CEBPB	chr5:105826569-105826777	HepG2	liver:	n/a	chr5:105826713-105826724
19	CEBPB	chr5:105937304-105937803	MCF-7	breast:	n/a	n/a
20	CEBPB	chr5:105893053-105893322	HepG2	liver:	n/a	chr5:105893187-105893198 chr5:105893189-105893200 chr5:105893187-105893200
21	CEBPB	chr5:105857479-105858427	A549	lung:	n/a	chr5:105858325-105858337
22	CEBPB	chr5:105937416-105937591	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr5:105902109-105902237	A549	lung:	n/a	n/a
24	CEBPB	chr5:105799818-105800083	H1-hESC	embryonic stem cell:	n/a	chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799959-105799970 chr5:105799959-105799972 chr5:105799961-105799970 chr5:105799960-105799971 chr5:105799862-105799874 chr5:105799959-105799972
25	CEBPB	chr5:105893027-105893313	A549	lung:	n/a	chr5:105893187-105893198 chr5:105893189-105893200 chr5:105893187-105893200
26	CEBPB	chr5:105813496-105813814	MCF-7	breast:	n/a	chr5:105813644-105813656
27	CEBPB	chr5:105935606-105935875	A549	lung:	n/a	chr5:105935743-105935756 chr5:105935745-105935754
28	CEBPB	chr5:105893061-105893350	IMR90	lung:	n/a	chr5:105893187-105893198 chr5:105893189-105893200 chr5:105893187-105893200
29	CEBPB	chr5:105799793-105800150	HepG2	liver:	n/a	chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799959-105799970 chr5:105799959-105799972 chr5:105799961-105799970 chr5:105799960-105799971 chr5:105799862-105799874 chr5:105799959-105799972
30	CEBPB	chr5:105814096-105814440	Hela-S3	cervix:	n/a	chr5:105814270-105814281
31	CEBPB	chr5:105799775-105800128	A549	lung:	n/a	chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799959-105799970 chr5:105799959-105799972 chr5:105799961-105799970 chr5:105799960-105799971 chr5:105799862-105799874 chr5:105799959-105799972
32	CEBPB	chr5:105937335-105937784	MCF-7	breast:	n/a	n/a
33	CEBPB	chr5:105859114-105859462	IMR90	lung:	n/a	chr5:105859114-105859125 chr5:105859284-105859295
34	CEBPB	chr5:105814124-105814357	A549	lung:	n/a	chr5:105814270-105814281
35	CEBPB	chr5:105799781-105800144	IMR90	lung:	n/a	chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799959-105799970 chr5:105799959-105799972 chr5:105799961-105799970 chr5:105799960-105799971 chr5:105799862-105799874 chr5:105799959-105799972
36	CEBPB	chr5:105941355-105941494	A549	lung:	n/a	n/a
37	CEBPB	chr5:105814101-105814422	HepG2	liver:	n/a	chr5:105814270-105814281
38	CEBPB	chr5:105891868-105892016	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr5:105891848-105892093	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:105859120-105859425	A549	lung:	n/a	chr5:105859284-105859295
41	CEBPB	chr5:105813435-105813964	MCF-7	breast:	n/a	chr5:105813644-105813656
42	CHD1	chr5:105871324-105871348	GM12878	blood:	n/a	n/a
43	CHD1	chr5:105936969-105937349	GM12878	blood:	n/a	n/a
44	CHD2	chr5:105871317-105871346	GM12878	blood:	n/a	n/a
45	CHD2	chr5:105936444-105936913	GM12878	blood:	n/a	n/a
46	CHD2	chr5:105937187-105937772	GM12878	blood:	n/a	n/a
47	CTCF	chr5:105939007-105939058	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr5:105975260-105975410	HCPEpiC	choroid plexus:	n/a	chr5:105975334-105975352 chr5:105975335-105975351
49	CTCF	chr5:105790480-105790630	GM12874	blood:	n/a	n/a
50	CTCF	chr5:105939039-105939077	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:105791135-105791185	Hepatocyte	liver:	n/a
2	chr5:105791135-105791185	AG10803	skin:	n/a
3	chr5:105791135-105791185	HCPEpiC	choroid plexus:	n/a
4	chr5:105791135-105791185	GM12892	blood:	n/a
5	chr5:105791135-105791185	HCM	heart:	n/a
6	chr5:105791135-105791185	K562	blood:	n/a
7	chr5:105791135-105791185	HIPEpiC	eye:	n/a
8	chr5:105791135-105791185	NHDF-neo	bronchial:	n/a
9	chr5:105791135-105791185	GM12891	blood:	n/a
10	chr5:105791135-105791185	AG09319	gingival:	n/a
11	chr5:105791135-105791185	RPTEC	kidney:	n/a
12	chr5:105791135-105791185	SK-N-SH_RA	brain:	n/a
13	chr5:105791135-105791185	MCF-7	breast:	n/a
14	chr5:105791135-105791185	GM06990	blood:	n/a
15	chr5:105791135-105791185	Jurkat	blood:	n/a
16	chr5:105791135-105791185	PANC-1	pancreas:	n/a
17	chr5:105791135-105791185	A549	lung:	n/a
18	chr5:105791135-105791185	HPAEpiC	pulmonary alveolar:	n/a
19	chr5:105791135-105791185	SK-N-SH	brain:	n/a
20	chr5:105791135-105791185	AoSMC	blood vessel:	n/a
21	chr5:105791135-105791185	AG04449	skin:	fetal
22	chr5:105791135-105791185	NB4	blood:	n/a
23	chr5:105791135-105791185	CMK	blood:	n/a
24	chr5:105791135-105791185	SAEC	small airway:	n/a
25	chr5:105791135-105791185	HRE	kidney:	n/a
26	chr5:105791135-105791185	HCF	heart:	n/a
27	chr5:105791135-105791185	BJ	skin:	n/a
28	chr5:105791135-105791185	IMR90	lung:	fetal
29	chr5:105791135-105791185	HEK293	kidney:	embryo
30	chr5:105791135-105791185	HAEpiC	amniotic membrane:	n/a
31	chr5:105791135-105791185	AG04450	lung:	fetal
32	chr5:105791135-105791185	MCF10A-Er-Src	breast:	n/a
33	chr5:105791135-105791185	PFSK-1	brain:	n/a
34	chr5:105791135-105791185	ECC-1	luminal epithelium:	n/a
35	chr5:105791135-105791185	BE2_C	brain:	n/a
36	chr5:105791135-105791185	HNPCEpiC	eye:	n/a
37	chr5:105791135-105791185	HUVEC	blood vessel:	n/a
38	chr5:105791135-105791185	Caco-2	colon:	n/a
39	chr5:105791135-105791185	PrEC	prostate:	n/a
40	chr5:105791135-105791185	HRCEpiC	kidney:	n/a
41	chr5:105791135-105791185	ovcar-3	ovarian:	n/a
42	chr5:105791135-105791185	HRPEpiC	eye:	n/a
43	chr5:105791135-105791185	HCT-116	colon:	n/a
44	chr5:105791135-105791185	GM12878	blood:	n/a
45	chr5:105791135-105791185	HepG2	liver:	n/a
46	chr5:105791135-105791185	ProgFib	skin:	n/a
47	chr5:105791135-105791185	NT2-D1	testis:	n/a
48	chr5:105791135-105791185	T-47D	breast:	n/a
49	chr5:105791135-105791185	GM19239	blood:	n/a
50	chr5:105791135-105791185	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:105971307..105972912-chr5:105974720..105977019,2	MCF-7	breast:
2	chr5:105971307..105972912-chr5:105974720..105977019,2	MCF-7	breast:
3	chr5:105790013..105791980-chr5:105793268..105795138,2	MCF-7	breast:
4	chr5:105938151..105940256-chr5:105942344..105944925,2	MCF-7	breast:
5	chr5:105907774..105910252-chr5:105911884..105914582,2	K562	blood:
6	chr5:105907774..105910252-chr5:105911884..105914582,2	K562	blood:
7	chr5:105907051..105910252-chr5:105911452..105914582,3	K562	blood:
8	chr5:105982713..105983578-chr7:143652953..143653920,2	MCF-7	breast:
9	chr5:105790013..105791980-chr5:105793268..105795138,2	MCF-7	breast:
10	chr5:105807775..105809773-chr5:105811667..105814083,2	MCF-7	breast:
11	chr5:52211080..52211594-chr5:105856085..105856865,2	MCF-7	breast:
12	chr5:105938151..105940256-chr5:105942344..105944925,2	MCF-7	breast:
13	chr5:105807775..105809773-chr5:105811667..105814083,2	MCF-7	breast:
14	chr5:105907051..105910252-chr5:105911452..105914582,3	K562	blood:

Variant related genes	Relation type
ENSG00000250145	TF binding region
ENSG00000252337	TF binding region
ENSG00000250145	CpG island
ENSG00000252337	CpG island

Extended variants
information (count: 2194 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2194 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564556952	chr5:105790540-105790541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs190221033	chr5:105790542-105790543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552796628	chr5:105790544-105790545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550106784	chr5:105790560-105790561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs74687836	chr5:105790570-105790571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144868426	chr5:105790618-105790619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114312572	chr5:105790622-105790623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138774127	chr5:105790639-105790640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs141743288	chr5:105790706-105790707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146255739	chr5:105790787-105790788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs965477	chr5:105790802-105790803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571399718	chr5:105790895-105790896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537336221	chr5:105790946-105790947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs77012855	chr5:105790955-105790956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182879876	chr5:105790964-105790965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549261289	chr5:105790970-105790971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370310889	chr5:105791009-105791010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535819025	chr5:105791087-105791088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186032459	chr5:105791124-105791125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115650034	chr5:105791140-105791141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139153633	chr5:105791190-105791191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs191921517	chr5:105791198-105791199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149472146	chr5:105791242-105791243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543617685	chr5:105791265-105791266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs972802	chr5:105791269-105791270	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs556103467	chr5:105791270-105791271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529559058	chr5:105791296-105791297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183660316	chr5:105791324-105791325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559115597	chr5:105791354-105791355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528187846	chr5:105791357-105791358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143965122	chr5:105791377-105791378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571330666	chr5:105791427-105791428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148602210	chr5:105791438-105791439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550819101	chr5:105791495-105791496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567529549	chr5:105791558-105791559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571634309	chr5:105791564-105791565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7449172	chr5:105791571-105791572	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs536384600	chr5:105791593-105791594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs386690802	chr5:105791594-105791595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555710193	chr5:105791595-105791596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572394360	chr5:105791596-105791597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535108729	chr5:105791597-105791598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557929267	chr5:105791599-105791600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577719118	chr5:105791600-105791601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149027744	chr5:105791601-105791602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs72790795	chr5:105791613-105791614	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs144236322	chr5:105791630-105791631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189153141	chr5:105791668-105791669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543000109	chr5:105791712-105791713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111531211	chr5:105791755-105791756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
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
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
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	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
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:141 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:105789000-105791400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:105789000-105791400	Enhancers	HMEC	breast
3	chr5:105789800-105791200	Enhancers	Brain Hippocampus Middle	brain
4	chr5:105790000-105790800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr5:105790000-105791000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:105790000-105791200	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr5:105790000-105791400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr5:105790000-105791400	Enhancers	NHEK	skin
9	chr5:105790200-105790600	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr5:105790200-105790800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr5:105790200-105790800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr5:105790200-105790800	Enhancers	Brain Angular Gyrus	brain
13	chr5:105790200-105791200	Enhancers	Osteobl	bone
14	chr5:105790400-105791000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr5:105790400-105791200	Enhancers	Muscle Satellite Cultured Cells	--
16	chr5:105790400-105791200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr5:105790400-105791200	Enhancers	Brain Anterior Caudate	brain
18	chr5:105790400-105791200	Enhancers	NH-A	brain
19	chr5:105790400-105791400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr5:105790600-105790800	Enhancers	Brain Cingulate Gyrus	brain
21	chr5:105790600-105791200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr5:105791200-105795600	Weak transcription	Osteobl	bone
23	chr5:105795600-105795800	Enhancers	Osteobl	bone
24	chr5:105809400-105810200	Enhancers	Fetal Heart	heart
25	chr5:105809800-105812200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr5:105813000-105814600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:105817000-105817800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr5:105817000-105818000	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr5:105817200-105817600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr5:105817200-105817600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr5:105824200-105824800	Enhancers	Osteobl	bone
32	chr5:105837200-105837800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
33	chr5:105843800-105844000	Enhancers	Fetal Heart	heart
34	chr5:105844200-105845200	Weak transcription	Fetal Heart	heart
35	chr5:105845200-105846200	Enhancers	Fetal Heart	heart
36	chr5:105846000-105846400	Enhancers	HMEC	breast
37	chr5:105846000-105846400	Enhancers	NHEK	skin
38	chr5:105846000-105846600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr5:105846200-105847800	Weak transcription	Fetal Heart	heart
40	chr5:105847800-105848600	Enhancers	Fetal Heart	heart
41	chr5:105855000-105855200	Enhancers	A549	lung
42	chr5:105855200-105855800	Weak transcription	A549	lung
43	chr5:105855800-105857200	Enhancers	A549	lung
44	chr5:105857000-105858800	Enhancers	HUVEC	blood vessel
45	chr5:105857200-105857600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr5:105857200-105857800	Enhancers	Brain Hippocampus Middle	brain
47	chr5:105857200-105858000	Flanking Active TSS	A549	lung
48	chr5:105857200-105858600	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr5:105857200-105859800	Enhancers	Muscle Satellite Cultured Cells	--
50	chr5:105857600-105858200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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