Variant report

Variant	nsv882769
Chromosome Location	chr5:118088385-118154368
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	ARID3A	chr5:118127755-118128035	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:118127746-118128030	K562	blood:	n/a	n/a
3	ATF1	chr5:118127812-118127974	K562	blood:	n/a	n/a
4	BATF	chr5:118112391-118112876	GM12878	blood:	n/a	n/a
5	BATF	chr5:118154342-118154589	GM12878	blood:	n/a	chr5:118154501-118154512
6	BHLHE40	chr5:118099612-118099828	GM12878	blood:	n/a	n/a
7	BRCA1	chr5:118125139-118125142	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr5:118097519-118097860	A549	lung:	n/a	chr5:118097688-118097699
9	CEBPB	chr5:118122013-118122244	HepG2	liver:	n/a	chr5:118122114-118122125
10	CEBPB	chr5:118112124-118112323	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr5:118097542-118097873	H1-hESC	embryonic stem cell:	n/a	chr5:118097688-118097699
12	CEBPB	chr5:118097516-118097870	HepG2	liver:	n/a	chr5:118097688-118097699
13	CEBPB	chr5:118097570-118097818	K562	blood:	n/a	chr5:118097688-118097699
14	CEBPB	chr5:118093504-118093672	IMR90	lung:	n/a	chr5:118093581-118093592
15	CEBPB	chr5:118116059-118116391	MCF-7	breast:	n/a	chr5:118116190-118116201
16	CEBPB	chr5:118122093-118122134	K562	blood:	n/a	chr5:118122114-118122125
17	CEBPB	chr5:118116037-118116329	HepG2	liver:	n/a	chr5:118116190-118116201
18	CEBPB	chr5:118097534-118097852	IMR90	lung:	n/a	chr5:118097688-118097699
19	CEBPB	chr5:118093476-118093677	HepG2	liver:	n/a	chr5:118093581-118093592
20	CHD1	chr5:118127521-118128226	IMR90	lung:	n/a	n/a
21	CHD2	chr5:118127832-118127833	K562	blood:	n/a	n/a
22	CTCF	chr5:118127860-118128010	GM12865	blood:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
23	CTCF	chr5:118127880-118128030	AoAF	blood vessel:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
24	CTCF	chr5:118127800-118127950	HA-sp	spinal cord:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
25	CTCF	chr5:118127840-118127990	HVMF	connective:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
26	CTCF	chr5:118125160-118125310	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr5:118127803-118128051	GM10248	blood:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
28	CTCF	chr5:118125245-118125343	MCF-7	breast:	n/a	n/a
29	CTCF	chr5:118128140-118128290	NHEK	skin:	n/a	n/a
30	CTCF	chr5:118127900-118128050	GM12801	blood:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
31	CTCF	chr5:118127740-118127890	HFF	foreskin:	n/a	n/a
32	CTCF	chr5:118125220-118125370	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr5:118127840-118127990	HMEC	breast:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
34	CTCF	chr5:118127812-118128041	MCF-7	breast:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
35	CTCF	chr5:118127756-118128023	T-47D	breast:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
36	CTCF	chr5:118127496-118128292	A549	lung:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
37	CTCF	chr5:118125240-118125390	MCF-7	breast:	n/a	n/a
38	CTCF	chr5:118094959-118095072	GM12878	blood:	n/a	n/a
39	CTCF	chr5:118125200-118125350	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr5:118127840-118127990	GM12869	blood:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
41	CTCF	chr5:118127820-118127970	GM12878	blood:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
42	CTCF	chr5:118127840-118127990	AoAF	blood vessel:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
43	CTCF	chr5:118127860-118128010	HBMEC	blood vessel:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
44	CTCF	chr5:118127826-118128049	Fibrobl	skin:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
45	CTCF	chr5:118127820-118127970	HA-sp	spinal cord:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
46	CTCF	chr5:118127840-118127990	GM12872	blood:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
47	CTCF	chr5:118127802-118128023	SK-N-SH_RA	brain:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
48	CTCF	chr5:118127880-118128030	GM12866	blood:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
49	CTCF	chr5:118127824-118128036	GM19239	blood:	n/a	chr5:118127908-118127924 chr5:118127907-118127925 chr5:118127909-118127922 chr5:118127902-118127923
50	CTCF	chr5:118127760-118127910	RPTEC	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:118132145-118132195	HepG2	liver:	n/a
2	chr5:118132145-118132195	AG09309	skin:	n/a
3	chr5:118132145-118132195	AoSMC	blood vessel:	n/a
4	chr5:118132145-118132195	K562	blood:	n/a
5	chr5:118132145-118132195	MCF-7	breast:	n/a
6	chr5:118132145-118132195	NH-A	brain:	n/a
7	chr5:118132145-118132195	GM12892	blood:	n/a
8	chr5:118132145-118132195	PFSK-1	brain:	n/a
9	chr5:118132145-118132195	HRPEpiC	eye:	n/a
10	chr5:118132145-118132195	AG04449	skin:	fetal
11	chr5:118132145-118132195	SKMC	muscle:	n/a
12	chr5:118132145-118132195	NB4	blood:	n/a
13	chr5:118132145-118132195	T-47D	breast:	n/a
14	chr5:118132145-118132195	HCF	heart:	n/a
15	chr5:118132145-118132195	HCT-116	colon:	n/a
16	chr5:118132145-118132195	GM19239	blood:	n/a
17	chr5:118132145-118132195	GM12878	blood:	n/a
18	chr5:118132145-118132195	ProgFib	skin:	n/a
19	chr5:118132145-118132195	HIPEpiC	eye:	n/a
20	chr5:118132145-118132195	HAEpiC	amniotic membrane:	n/a
21	chr5:118132145-118132195	SK-N-MC	brain:	n/a
22	chr5:118132145-118132195	HMEC	breast:	n/a
23	chr5:118132145-118132195	Jurkat	blood:	n/a
24	chr5:118132145-118132195	Caco-2	colon:	n/a
25	chr5:118132145-118132195	NT2-D1	testis:	n/a
26	chr5:118132145-118132195	HNPCEpiC	eye:	n/a
27	chr5:118132145-118132195	AG04450	lung:	fetal
28	chr5:118132145-118132195	ECC-1	luminal epithelium:	n/a
29	chr5:118132145-118132195	HCPEpiC	choroid plexus:	n/a
30	chr5:118132145-118132195	A549	lung:	n/a
31	chr5:118132145-118132195	NHDF-neo	bronchial:	n/a
32	chr5:118132145-118132195	RPTEC	kidney:	n/a
33	chr5:118132145-118132195	SK-N-SH_RA	brain:	n/a
34	chr5:118132145-118132195	HRCEpiC	kidney:	n/a
35	chr5:118132145-118132195	AG10803	skin:	n/a
36	chr5:118132145-118132195	ovcar-3	ovarian:	n/a
37	chr5:118132145-118132195	NHBE	bronchial:	n/a
38	chr5:118132145-118132195	HL-60	blood:	n/a
39	chr5:118132145-118132195	PrEC	prostate:	n/a
40	chr5:118132145-118132195	AG09319	gingival:	n/a
41	chr5:118132145-118132195	BE2_C	brain:	n/a
42	chr5:118132145-118132195	HUVEC	blood vessel:	n/a
43	chr5:118132145-118132195	H1-hESC	embryonic stem cell:	embryo
44	chr5:118132145-118132195	MCF10A-Er-Src	breast:	n/a
45	chr5:118132145-118132195	SK-N-SH	brain:	n/a
46	chr5:118132145-118132195	U87	brain:	n/a
47	chr5:118132145-118132195	SAEC	small airway:	n/a
48	chr5:118132145-118132195	HEK293	kidney:	embryo
49	chr5:118132145-118132195	GM06990	blood:	n/a
50	chr5:118132145-118132195	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:118097213..118099341-chr5:118103598..118106266,2	K562	blood:
2	chr5:118111304..118112111-chr5:118225562..118226077,2	MCF-7	breast:
3	chr5:117947053..117948753-chr5:118127871..118130563,2	MCF-7	breast:
4	chr5:118126334..118128715-chr5:118291929..118293772,2	MCF-7	breast:
5	chr5:118123238..118126072-chr5:118128175..118130708,2	MCF-7	breast:
6	chr5:117345316..117346227-chr5:118111319..118112071,2	MCF-7	breast:
7	chr5:117946766..117947670-chr5:118127610..118128249,2	MCF-7	breast:
8	chr5:118097213..118099341-chr5:118103598..118106266,2	K562	blood:
9	chr5:118140828..118142755-chr5:118221049..118222690,2	K562	blood:
10	chr5:118111874..118114784-chr5:118117605..118120006,2	K562	blood:
11	chr5:117345316..117346232-chr5:118111290..118112171,4	MCF-7	breast:
12	chr5:118115173..118117951-chr5:118120294..118122850,2	K562	blood:
13	chr5:118111874..118114784-chr5:118117605..118120006,2	K562	blood:
14	chr5:118123238..118126072-chr5:118128175..118130708,2	MCF-7	breast:
15	chr16:14311721..14312241-chr5:118127410..118128139,2	MCF-7	breast:
16	chr5:118122820..118124504-chr5:118126340..118128643,2	K562	blood:
17	chr5:118122820..118124504-chr5:118126340..118128643,2	K562	blood:
18	chr5:117345575..117346316-chr5:118111227..118112029,2	MCF-7	breast:
19	chr5:116822706..116823238-chr5:118110990..118112031,3	MCF-7	breast:
20	chr5:118146966..118149409-chr5:118153025..118155209,2	K562	blood:
21	chr5:118034173..118035130-chr5:118126969..118128409,6	MCF-7	breast:
22	chr5:117953386..117954146-chr5:118127518..118128022,2	MCF-7	breast:
23	chr5:118146966..118149409-chr5:118153025..118155209,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DTWD2-2	chr5:118121037-118121154	XLOC_004966
2	lnc-DTWD2-6	chr5:118101197-118101249	l_3003_chr5:118060532-118101249_testes
3	lnc-DTWD2-2	chr5:118096169-118096547	XLOC_004966
4	lnc-DTWD2-6	chr5:118098817-118098860	l_3003_chr5:118060532-118101249_testes

Variant related genes	Relation type
ENSG00000249426	TF binding region
RNU7-34P	TF binding region
ENSG00000249426	CpG island
RNU7-34P	CpG island
ENSG00000249426	chromatin interactions

Extended variants
information (count: 2202 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2202 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs677881	chr5:118088385-118088386	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567913666	chr5:118088393-118088394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536889202	chr5:118088402-118088403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190313462	chr5:118088414-118088415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139314371	chr5:118088418-118088419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs10658414	chr5:118088457-118088458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs66526603	chr5:118088458-118088459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs141231111	chr5:118088461-118088462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs200156981	chr5:118088463-118088464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs142036796	chr5:118088478-118088479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs77882879	chr5:118088479-118088480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs56089675	chr5:118088480-118088481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182130885	chr5:118088511-118088512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs17144543	chr5:118088544-118088545	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs541706449	chr5:118088575-118088576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528123066	chr5:118088909-118088910	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs111688996	chr5:118088950-118088951	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs111923377	chr5:118089007-118089008	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs567976407	chr5:118089016-118089017	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs116619577	chr5:118089018-118089019	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs541697635	chr5:118089029-118089030	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs2973619	chr5:118089215-118089216	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs188381424	chr5:118089223-118089224	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs2972218	chr5:118089236-118089237	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs147126210	chr5:118089240-118089241	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs575119904	chr5:118089249-118089250	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs545742684	chr5:118089252-118089253	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs191689933	chr5:118089254-118089255	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs72784007	chr5:118089463-118089464	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs141856743	chr5:118089486-118089487	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs186137195	chr5:118090623-118090624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541491682	chr5:118090624-118090625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs564130207	chr5:118090692-118090693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs575448684	chr5:118090703-118090704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533044336	chr5:118090734-118090735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540552965	chr5:118090740-118090741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527634816	chr5:118090786-118090787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs17144549	chr5:118090812-118090813	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs190066774	chr5:118090818-118090819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs17144550	chr5:118090832-118090833	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs557701425	chr5:118090849-118090850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530251901	chr5:118090853-118090854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs635718	chr5:118090860-118090861	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs550966344	chr5:118090861-118090862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181434976	chr5:118090873-118090874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs539731576	chr5:118090909-118090910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs144149295	chr5:118090933-118090934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs58999502	chr5:118090959-118090960	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs535693916	chr5:118090979-118090980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555543090	chr5:118091007-118091008	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
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
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
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:216 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:118088200-118088600	Enhancers	Fetal Lung	lung
2	chr5:118090600-118091400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:118092200-118092600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:118097400-118098200	Enhancers	Fetal Heart	heart
5	chr5:118097600-118098400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr5:118097600-118098600	Enhancers	Pancreas	Pancrea
7	chr5:118103600-118105400	Enhancers	Liver	Liver
8	chr5:118106600-118107000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr5:118107000-118110200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr5:118109000-118112600	Weak transcription	Pancreas	Pancrea
11	chr5:118109400-118111800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:118109800-118110400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr5:118110200-118110400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr5:118110200-118110400	Enhancers	Left Ventricle	heart
15	chr5:118110200-118110400	Enhancers	GM12878-XiMat	blood
16	chr5:118110200-118110800	Enhancers	Ovary	ovary
17	chr5:118110400-118111600	Weak transcription	GM12878-XiMat	blood
18	chr5:118110800-118111800	Weak transcription	Ovary	ovary
19	chr5:118111600-118112200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr5:118111600-118113000	Enhancers	GM12878-XiMat	blood
21	chr5:118111600-118113400	Enhancers	Liver	Liver
22	chr5:118111800-118112000	Enhancers	Ovary	ovary
23	chr5:118112000-118113600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr5:118112600-118113600	Enhancers	Pancreas	Pancrea
25	chr5:118112800-118113600	Enhancers	Duodenum Mucosa	Duodenum
26	chr5:118113600-118115800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr5:118115600-118116800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr5:118115800-118116000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr5:118116000-118116400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr5:118116000-118116600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr5:118116200-118116600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr5:118117600-118118000	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr5:118117800-118118200	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr5:118118400-118126400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:118119400-118120600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr5:118120600-118121600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr5:118121400-118121800	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr5:118121600-118121800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr5:118121600-118122000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr5:118121800-118127000	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr5:118122000-118127200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr5:118124800-118125400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr5:118124800-118125600	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr5:118125000-118125200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr5:118125000-118125200	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr5:118125000-118125400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr5:118125000-118125400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr5:118125200-118126600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr5:118125200-118127000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr5:118125200-118127600	Weak transcription	HUES6 Cell Line	embryonic stem cell

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