Variant report

Variant	nsv462403
Chromosome Location	chr5:115994775-116284378
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2263)
CpG islands
(count:795)
Chromatin interactive
region (count:31)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2263 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:116283657-116283951	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:116102107-116102543	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:116194659-116194984	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:116217836-116218042	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:116101168-116101512	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:116198385-116200736	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:116012471-116012696	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:116135107-116135388	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:116104996-116105536	HepG2	liver:	n/a	n/a
10	ATF1	chr5:116102266-116102552	K562	blood:	n/a	n/a
11	ATF2	chr5:116099450-116100317	GM12878	blood:	n/a	n/a
12	ATF2	chr5:116006612-116007415	GM12878	blood:	n/a	n/a
13	ATF2	chr5:116283643-116284032	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr5:116200059-116200723	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr5:116219491-116220039	GM12878	blood:	n/a	n/a
16	ATF2	chr5:116038413-116038924	GM12878	blood:	n/a	n/a
17	ATF2	chr5:116098888-116099364	GM12878	blood:	n/a	n/a
18	ATF2	chr5:116040484-116040840	GM12878	blood:	n/a	n/a
19	ATF2	chr5:116017218-116017856	GM12878	blood:	n/a	n/a
20	ATF2	chr5:116044698-116045107	GM12878	blood:	n/a	n/a
21	ATF2	chr5:116009044-116009661	GM12878	blood:	n/a	n/a
22	ATF2	chr5:116009058-116009517	GM12878	blood:	n/a	n/a
23	ATF2	chr5:116101965-116102666	GM12878	blood:	n/a	n/a
24	ATF2	chr5:116017130-116018132	GM12878	blood:	n/a	n/a
25	ATF2	chr5:116006717-116007402	GM12878	blood:	n/a	n/a
26	ATF2	chr5:116032002-116032492	GM12878	blood:	n/a	n/a
27	ATF2	chr5:116102043-116102677	GM12878	blood:	n/a	n/a
28	ATF2	chr5:116258221-116258693	GM12878	blood:	n/a	n/a
29	ATF2	chr5:116200021-116200818	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr5:116040340-116040904	GM12878	blood:	n/a	n/a
31	ATF2	chr5:116032024-116032488	GM12878	blood:	n/a	n/a
32	ATF2	chr5:116038296-116038886	GM12878	blood:	n/a	n/a
33	ATF2	chr5:116099485-116100318	GM12878	blood:	n/a	n/a
34	ATF2	chr5:116283512-116283962	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF2	chr5:116098877-116099341	GM12878	blood:	n/a	n/a
36	ATF2	chr5:116283536-116283941	GM12878	blood:	n/a	n/a
37	ATF3	chr5:116102244-116102534	K562	blood:	n/a	n/a
38	ATF3	chr5:116102087-116102580	HCT-116	colon:	n/a	n/a
39	BACH1	chr5:116283620-116284007	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr5:116099882-116099886	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr5:116095642-116096244	H1-hESC	embryonic stem cell:	n/a	n/a
42	BATF	chr5:116076654-116076931	GM12878	blood:	n/a	n/a
43	BATF	chr5:116044769-116045242	GM12878	blood:	n/a	n/a
44	BATF	chr5:116054036-116054315	GM12878	blood:	n/a	n/a
45	BATF	chr5:116221539-116221782	GM12878	blood:	n/a	n/a
46	BATF	chr5:116241552-116241844	GM12878	blood:	n/a	n/a
47	BATF	chr5:116040310-116040833	GM12878	blood:	n/a	n/a
48	BATF	chr5:116219676-116219912	GM12878	blood:	n/a	n/a
49	BATF	chr5:116032042-116032459	GM12878	blood:	n/a	chr5:116032278-116032289
50	BATF	chr5:116098647-116098889	GM12878	blood:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:116150282-116150332	GM12891	blood:	n/a
2	chr5:116191725-116191775	PANC-1	pancreas:	n/a
3	chr5:116150282-116150332	GM12891	blood:	n/a
4	chr5:116191725-116191775	PANC-1	pancreas:	n/a
5	chr5:116197864-116197914	AG09319	gingival:	n/a
6	chr5:116259413-116259463	AG04450	lung:	fetal
7	chr5:116039174-116039224	BE2_C	brain:	n/a
8	chr5:116069988-116070038	GM06990	blood:	n/a
9	chr5:116108611-116108661	HEEpiC	esophagus:	n/a
10	chr5:116089180-116089230	GM12878	blood:	n/a
11	chr5:116191725-116191775	ovcar-3	ovarian:	n/a
12	chr5:116032334-116032384	BJ	skin:	n/a
13	chr5:116259413-116259463	PFSK-1	brain:	n/a
14	chr5:116274667-116274717	U87	brain:	n/a
15	chr5:116108611-116108661	NT2-D1	testis:	n/a
16	chr5:116280275-116280325	HCPEpiC	choroid plexus:	n/a
17	chr5:116197864-116197914	HepG2	liver:	n/a
18	chr5:116191725-116191775	GM06990	blood:	n/a
19	chr5:116032334-116032384	SAEC	small airway:	n/a
20	chr5:116150282-116150332	PANC-1	pancreas:	n/a
21	chr5:116108611-116108661	BE2_C	brain:	n/a
22	chr5:116197864-116197914	NHDF-neo	bronchial:	n/a
23	chr5:116075820-116075870	NH-A	brain:	n/a
24	chr5:116274667-116274717	GM06990	blood:	n/a
25	chr5:116259413-116259463	MCF10A-Er-Src	breast:	n/a
26	chr5:116113889-116113939	LNCaP	prostate:	n/a
27	chr5:116089180-116089230	HCF	heart:	n/a
28	chr5:116108611-116108661	SK-N-SH	brain:	n/a
29	chr5:116032334-116032384	Hela-S3	cervix:	n/a
30	chr5:116039174-116039224	ECC-1	luminal epithelium:	n/a
31	chr5:116089180-116089230	U87	brain:	n/a
32	chr5:116280275-116280325	HCM	heart:	n/a
33	chr5:116039174-116039224	ovcar-3	ovarian:	n/a
34	chr5:116069988-116070038	SKMC	muscle:	n/a
35	chr5:116150282-116150332	ECC-1	luminal epithelium:	n/a
36	chr5:116032334-116032384	HEK293	kidney:	embryo
37	chr5:116280275-116280325	T-47D	breast:	n/a
38	chr5:116191725-116191775	AoSMC	blood vessel:	n/a
39	chr5:116108611-116108661	Caco-2	colon:	n/a
40	chr5:116197864-116197914	T-47D	breast:	n/a
41	chr5:116191725-116191775	BE2_C	brain:	n/a
42	chr5:116259413-116259463	HAEpiC	amniotic membrane:	n/a
43	chr5:116150282-116150332	NB4	blood:	n/a
44	chr5:116191725-116191775	A549	lung:	n/a
45	chr5:116197864-116197914	H1-hESC	embryonic stem cell:	embryo
46	chr5:116197864-116197914	HL-60	blood:	n/a
47	chr5:116259413-116259463	SKMC	muscle:	n/a
48	chr5:116039174-116039224	SK-N-SH_RA	brain:	n/a
49	chr5:116032334-116032384	HRCEpiC	kidney:	n/a
50	chr5:116150282-116150332	HIPEpiC	eye:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:116052297..116054346-chr5:116056062..116057834,2	K562	blood:
2	chr5:116216466..116219443-chr5:116220949..116224827,3	MCF-7	breast:
3	chr5:116016880..116019114-chr5:116028567..116031024,2	K562	blood:
4	chr5:116141325..116143664-chr5:116165603..116167947,2	K562	blood:
5	chr5:116052297..116054346-chr5:116056062..116057834,2	K562	blood:
6	chr5:116013029..116014668-chr5:116015012..116017658,2	MCF-7	breast:
7	chr5:116197562..116200213-chr5:116281914..116283961,2	MCF-7	breast:
8	chr5:116019394..116021090-chr5:116023279..116025615,2	K562	blood:
9	chr5:116019394..116021090-chr5:116023279..116025615,2	K562	blood:
10	chr5:116197562..116200213-chr5:116281914..116283961,2	MCF-7	breast:
11	chr5:116073007..116074570-chr5:116076302..116077894,2	K562	blood:
12	chr5:116016880..116019114-chr5:116028567..116031024,2	K562	blood:
13	chr5:116073007..116074570-chr5:116076302..116077894,2	K562	blood:
14	chr1:144532509..144534121-chr5:116081146..116082646,2	K562	blood:
15	chr5:115911257..115912668-chr5:116283296..116284268,6	MCF-7	breast:
16	chr1:115633937..115636511-chr5:116028775..116031505,2	MCF-7	breast:
17	chr5:116216466..116219443-chr5:116220949..116224827,3	MCF-7	breast:
18	chr5:116159664..116161786-chr5:116162291..116165318,3	MCF-7	breast:
19	chr5:116013029..116014668-chr5:116015012..116017658,2	MCF-7	breast:
20	chr1:17233138..17234733-chr5:116082626..116084126,2	MCF-7	breast:
21	chr5:115991090..115992794-chr5:115993222..115995849,2	MCF-7	breast:
22	chr5:115910211..115911945-chr5:116200966..116203942,2	MCF-7	breast:
23	chr5:115972527..115974752-chr5:116000489..116003190,2	K562	blood:
24	chr3:155925817..155926573-chr5:116060845..116061700,2	MCF-7	breast:
25	chr5:116274317..116277091-chr5:116277592..116280132,2	MCF-7	breast:
26	chr5:116000364..116002050-chr5:116002499..116004214,2	MCF-7	breast:
27	chr5:116274317..116277091-chr5:116277592..116280132,2	MCF-7	breast:
28	chr5:115473291..115473804-chr5:116283477..116284254,2	MCF-7	breast:
29	chr5:116159664..116161786-chr5:116162291..116165318,3	MCF-7	breast:
30	chr5:115911320..115912473-chr5:116283341..116284236,4	MCF-7	breast:
31	chr5:116000364..116002050-chr5:116002499..116004214,2	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEMA6A-3	chr5:116096379-116096485	NR_104678
2	lnc-COMMD10-10	chr5:116147785-116149816	NONHSAT103378
3	lnc-SEMA6A-6	chr5:116030922-116031274	FPKM1_group_26180_transcript_1
4	lnc-COMMD10-11	chr5:116282030-116282143	NONHSAT103381
5	lnc-SEMA6A-6	chr5:116040765-116040866	NONHSAT103376
6	lnc-SEMA6A-6	chr5:116032091-116032233	FPKM1_group_26180_transcript_1
7	lnc-SEMA6A-3	chr5:116096379-116096485	XLOC_004962
8	lnc-SEMA6A-6	chr5:116025841-116025895	FPKM1_group_26180_transcript_1
9	lnc-SEMA6A-6	chr5:116032091-116032405	NONHSAT103376
10	lnc-SEMA6A-3	chr5:116097825-116097905	NR_104678
11	lnc-SEMA6A-6	chr5:116040765-116040866	FPKM1_group_26180_transcript_1
12	lnc-SEMA6A-3	chr5:116096591-116096711	XLOC_004962
13	lnc-COMMD10-11	chr5:116281744-116281873	NONHSAT103381
14	lnc-COMMD10-10	chr5:116143614-116143900	NONHSAT103378
15	lnc-SEMA6A-3	chr5:116078998-116079084	NR_104678
16	lnc-SEMA6A-3	chr5:116097825-116097905	XLOC_004962
17	lnc-SEMA6A-6	chr5:116030922-116031274	NONHSAT103376
18	lnc-SEMA6A-6	chr5:116032238-116032405	FPKM1_group_26180_transcript_1
19	lnc-COMMD10-10	chr5:116145051-116147613	NONHSAT103378
20	lnc-SEMA6A-6	chr5:116025841-116025895	NONHSAT103376
21	lnc-SEMA6A-3	chr5:116096591-116096711	NR_104678
22	lnc-SEMA6A-3	chr5:116078687-116079084	XLOC_004962

No data

Variant related genes	Relation type
ENSG00000251311	TF binding region
ENSG00000249150	TF binding region
RPS17P2	TF binding region
ENSG00000251311	CpG island
ENSG00000249150	CpG island
RPS17P2	CpG island
ENSG00000092421	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000249150	chromatin interactions

Extended variants
information (count: 11672 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:11672 , 50 per page) page: 1 2 3 4 5 6 7 ... 234

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1948429	chr5:115994775-115994776	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs115737159	chr5:115994876-115994877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs59431456	chr5:115994909-115994910	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs116273138	chr5:115994916-115994917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143904783	chr5:115994941-115994942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs114931722	chr5:115994950-115994951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150621615	chr5:115994966-115994967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555664255	chr5:115995005-115995006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575820854	chr5:115995009-115995010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531194600	chr5:115995027-115995028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544574081	chr5:115995120-115995121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139676367	chr5:115995130-115995131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs978493	chr5:115995141-115995142	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs375514211	chr5:115995158-115995159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183188213	chr5:115995184-115995185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560494314	chr5:115995281-115995282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529391336	chr5:115995296-115995297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs57404853	chr5:115995346-115995347	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs187477741	chr5:115995405-115995406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192617664	chr5:115995451-115995452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149855887	chr5:115995494-115995495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371096087	chr5:115995511-115995512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533079633	chr5:115995532-115995533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546151961	chr5:115995585-115995586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566163252	chr5:115995614-115995615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144818035	chr5:115995623-115995624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555483213	chr5:115995638-115995639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs76071325	chr5:115995671-115995672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs6883931	chr5:115995681-115995682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144450413	chr5:115995703-115995704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557789634	chr5:115995719-115995720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs578241413	chr5:115995740-115995741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540965310	chr5:115995759-115995760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75013099	chr5:115995769-115995770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574131888	chr5:115995806-115995807	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs185478569	chr5:115995844-115995845	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs562958777	chr5:115995876-115995877	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs62373642	chr5:115995888-115995889	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs531713648	chr5:115995893-115995894	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs56252192	chr5:115996014-115996015	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564138849	chr5:115996017-115996018	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553129635	chr5:115996073-115996074	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568508966	chr5:115996112-115996113	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547255182	chr5:115996165-115996166	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35009251	chr5:115996180-115996181	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190530256	chr5:115996183-115996184	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546517108	chr5:115996186-115996187	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs116582068	chr5:115996224-115996225	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528896164	chr5:115996271-115996272	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548706510	chr5:115996276-115996277	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1787 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115987600-115996400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:115989400-115996400	Weak transcription	Fetal Stomach	stomach
3	chr5:115990800-115995800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:115991600-115996200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr5:115992600-115997000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr5:115993400-115995000	Enhancers	NHEK	skin
7	chr5:115993600-115994800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr5:115993600-115994800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr5:115993800-115995000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr5:115993800-115995000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr5:115993800-115995000	Enhancers	HMEC	breast
12	chr5:115994000-115994800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr5:115994000-115995000	Enhancers	GM12878-XiMat	blood
14	chr5:115994600-115997200	Weak transcription	Brain Hippocampus Middle	brain
15	chr5:115995000-115996200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr5:115995800-115998800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:115996000-115996400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr5:115996200-115996600	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr5:115996200-115997800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr5:115996200-115997800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chr5:115996400-115997600	ZNF genes & repeats	Fetal Stomach	stomach
22	chr5:115996400-115997800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr5:115996400-115997800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr5:115996600-115997000	Flanking Bivalent TSS/Enh	HepG2	liver
25	chr5:115996600-115997400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:115996600-115997800	ZNF genes & repeats	Lung	lung
27	chr5:115996800-115997000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr5:115996800-115997600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
29	chr5:115997000-115997200	Bivalent Enhancer	HepG2	liver
30	chr5:115997000-115997600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr5:115997400-115997600	ZNF genes & repeats	Brain Hippocampus Middle	brain
32	chr5:115997800-115998200	Weak transcription	Brain Hippocampus Middle	brain
33	chr5:115997800-116000600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr5:115997800-116006000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr5:115998800-116003600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr5:116000600-116001200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr5:116000800-116001200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr5:116001200-116007000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr5:116002800-116003000	Enhancers	Psoas Muscle	Psoas
40	chr5:116002800-116003600	Enhancers	GM12878-XiMat	blood
41	chr5:116003400-116004800	Enhancers	HepG2	liver
42	chr5:116003600-116003800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:116003600-116003800	Weak transcription	Brain Hippocampus Middle	brain
44	chr5:116003600-116005600	Weak transcription	GM12878-XiMat	blood
45	chr5:116003600-116013400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr5:116003800-116004000	Enhancers	Brain Hippocampus Middle	brain
47	chr5:116003800-116004200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:116004000-116004800	Weak transcription	Brain Hippocampus Middle	brain
49	chr5:116004200-116004400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr5:116004400-116006000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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