Variant report

Variant	nsv462574
Chromosome Location	chr5:178269682-178313078
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:725)
CpG islands
(count:1100)
Chromatin interactive
region (count:27)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:725 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178286713-178287002	HepG2	liver:	n/a	n/a
2	ATF1	chr5:178286762-178287220	K562	blood:	n/a	n/a
3	ATF2	chr5:178286589-178286974	GM12878	blood:	n/a	n/a
4	ATF3	chr5:178286755-178287144	K562	blood:	n/a	n/a
5	ATF3	chr5:178286654-178287084	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:178286831-178287481	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr5:178299147-178299711	K562	blood:	n/a	n/a
8	BACH1	chr5:178299171-178299685	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCLAF1	chr5:178286705-178287046	K562	blood:	n/a	n/a
10	BCLAF1	chr5:178286646-178287185	GM12878	blood:	n/a	n/a
11	BCLAF1	chr5:178286652-178287189	GM12878	blood:	n/a	n/a
12	BHLHE40	chr5:178286636-178287416	K562	blood:	n/a	chr5:178287282-178287298 chr5:178287277-178287293
13	BHLHE40	chr5:178281482-178281689	HepG2	liver:	n/a	n/a
14	BHLHE40	chr5:178286715-178287439	HepG2	liver:	n/a	chr5:178287282-178287298 chr5:178287277-178287293
15	BHLHE40	chr5:178286530-178287352	GM12878	blood:	n/a	chr5:178287282-178287298 chr5:178287277-178287293
16	BHLHE40	chr5:178281355-178281697	K562	blood:	n/a	n/a
17	BRCA1	chr5:178286778-178287148	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr5:178286775-178286962	HepG2	liver:	n/a	n/a
19	CBX3	chr5:178286504-178287357	HCT-116	colon:	n/a	n/a
20	CBX3	chr5:178286622-178287208	K562	blood:	n/a	n/a
21	CBX3	chr5:178310545-178310982	K562	blood:	n/a	n/a
22	CBX3	chr5:178310127-178310478	K562	blood:	n/a	n/a
23	CCNT2	chr5:178281392-178281608	K562	blood:	n/a	n/a
24	CCNT2	chr5:178286759-178287496	K562	blood:	n/a	n/a
25	CEBPB	chr5:178286811-178287376	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr5:178293795-178293858	HepG2	liver:	n/a	n/a
27	CEBPB	chr5:178285796-178285889	K562	blood:	n/a	n/a
28	CEBPD	chr5:178286868-178287258	HepG2	liver:	n/a	n/a
29	CEBPD	chr5:178281357-178281709	K562	blood:	n/a	n/a
30	CHD1	chr5:178286816-178287274	GM12878	blood:	n/a	n/a
31	CHD2	chr5:178286820-178287177	K562	blood:	n/a	n/a
32	CHD2	chr5:178286711-178287474	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr5:178286713-178287176	HepG2	liver:	n/a	n/a
34	CHD2	chr5:178286747-178287356	GM12878	blood:	n/a	n/a
35	CHD2	chr5:178281396-178281607	K562	blood:	n/a	n/a
36	CHD2	chr5:178286719-178287176	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr5:178286710-178287214	A549	lung:	n/a	n/a
38	CREB1	chr5:178286648-178287231	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr5:178286629-178287486	HepG2	liver:	n/a	n/a
40	CREB1	chr5:178286704-178287340	GM12878	blood:	n/a	n/a
41	CREB1	chr5:178286681-178287337	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr5:178286820-178286970	HPF	lung:	n/a	n/a
43	CTCF	chr5:178286856-178287105	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:178286820-178286970	HCFaa	heart:	n/a	n/a
45	CTCF	chr5:178286960-178287110	GM12878	blood:	n/a	n/a
46	CTCF	chr5:178289710-178289785	K562	blood:	n/a	n/a
47	CTCF	chr5:178286780-178286930	GM12872	blood:	n/a	n/a
48	CTCF	chr5:178286920-178287070	NHEK	skin:	n/a	n/a
49	CTCF	chr5:178286840-178286990	MCF-7	breast:	n/a	n/a
50	CTCF	chr5:178287020-178287170	GM12874	blood:	n/a	chr5:178287151-178287164

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178285999-178286049	A549	lung:	n/a
2	chr5:178286892-178286942	SKMC	muscle:	n/a
3	chr5:178285999-178286049	A549	lung:	n/a
4	chr5:178286892-178286942	SKMC	muscle:	n/a
5	chr5:178283861-178283911	A549	lung:	n/a
6	chr5:178287112-178287162	A549	lung:	n/a
7	chr5:178291250-178291300	IMR90	lung:	fetal
8	chr5:178286626-178286676	HCPEpiC	choroid plexus:	n/a
9	chr5:178286881-178286931	K562	blood:	n/a
10	chr5:178287544-178287594	GM12878	blood:	n/a
11	chr5:178287767-178287817	AG10803	skin:	n/a
12	chr5:178287445-178287495	NHBE	bronchial:	n/a
13	chr5:178288650-178288700	GM12892	blood:	n/a
14	chr5:178291250-178291300	HepG2	liver:	n/a
15	chr5:178286735-178286785	PANC-1	pancreas:	n/a
16	chr5:178286892-178286942	HEEpiC	esophagus:	n/a
17	chr5:178288625-178288675	A549	lung:	n/a
18	chr5:178287544-178287594	Hela-S3	cervix:	n/a
19	chr5:178286881-178286931	HAEpiC	amniotic membrane:	n/a
20	chr5:178283861-178283911	U87	brain:	n/a
21	chr5:178287445-178287495	HRPEpiC	eye:	n/a
22	chr5:178285999-178286049	GM06990	blood:	n/a
23	chr5:178288650-178288700	HRCEpiC	kidney:	n/a
24	chr5:178286892-178286942	SK-N-MC	brain:	n/a
25	chr5:178285999-178286049	HCF	heart:	n/a
26	chr5:178286892-178286942	HCT-116	colon:	n/a
27	chr5:178287544-178287594	AG04449	skin:	fetal
28	chr5:178288687-178288737	SK-N-SH_RA	brain:	n/a
29	chr5:178287767-178287817	U87	brain:	n/a
30	chr5:178286892-178286942	RPTEC	kidney:	n/a
31	chr5:178283861-178283911	NHDF-neo	bronchial:	n/a
32	chr5:178286735-178286785	GM12891	blood:	n/a
33	chr5:178286735-178286785	GM12892	blood:	n/a
34	chr5:178288650-178288700	HRPEpiC	eye:	n/a
35	chr5:178288359-178288409	HEEpiC	esophagus:	n/a
36	chr5:178288359-178288409	HepG2	liver:	n/a
37	chr5:178287445-178287495	AG10803	skin:	n/a
38	chr5:178286892-178286942	HUVEC	blood vessel:	n/a
39	chr5:178291250-178291300	SK-N-SH_RA	brain:	n/a
40	chr5:178288625-178288675	HIPEpiC	eye:	n/a
41	chr5:178288687-178288737	PANC-1	pancreas:	n/a
42	chr5:178286892-178286942	HNPCEpiC	eye:	n/a
43	chr5:178286735-178286785	AG09309	skin:	n/a
44	chr5:178286735-178286785	NB4	blood:	n/a
45	chr5:178288359-178288409	AG10803	skin:	n/a
46	chr5:178286892-178286942	HCPEpiC	choroid plexus:	n/a
47	chr5:178286735-178286785	MCF-7	breast:	n/a
48	chr5:178291250-178291300	T-47D	breast:	n/a
49	chr5:178286857-178286907	HMEC	breast:	n/a
50	chr5:178291250-178291300	SAEC	small airway:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:178285493..178288791-chr5:178303197..178305318,3	MCF-7	breast:
2	chr5:178264186..178266313-chr5:178270488..178273068,2	MCF-7	breast:
3	chr5:178290096..178292803-chr5:178294356..178296794,2	K562	blood:
4	chr5:178154802..178159439-chr5:178284936..178288781,7	MCF-7	breast:
5	chr5:178285911..178288443-chr5:178294689..178296630,2	K562	blood:
6	chr5:178157243..178158078-chr5:178286943..178287443,2	MCF-7	breast:
7	chr5:178152146..178155385-chr5:178293103..178294784,3	MCF-7	breast:
8	chr5:178290096..178292803-chr5:178294356..178296794,2	K562	blood:
9	chr5:178156014..178158845-chr5:178285994..178289826,5	MCF-7	breast:
10	chr5:178157230..178157844-chr5:178286636..178287441,3	MCF-7	breast:
11	chr5:178299499..178302283-chr5:178303072..178304596,2	MCF-7	breast:
12	chr13:38619641..38620162-chr5:178301644..178302146,3	MCF-7	breast:
13	chr5:178286798..178288918-chr5:178487242..178488938,2	MCF-7	breast:
14	chr5:178266086..178268148-chr5:178277968..178280958,2	MCF-7	breast:
15	chr5:178053391..178055177-chr5:178285758..178288394,2	MCF-7	breast:
16	chr5:178279881..178281408-chr5:178284466..178287127,2	MCF-7	breast:
17	chr5:178276049..178278354-chr5:178322079..178324403,2	MCF-7	breast:
18	chr5:178285646..178289279-chr5:178321547..178324884,4	MCF-7	breast:
19	chr5:178262543..178264784-chr5:178273613..178275521,2	K562	blood:
20	chr5:178157412..178158250-chr5:178286406..178286923,4	MCF-7	breast:
21	chr13:38619618..38620640-chr5:178301624..178302148,7	MCF-7	breast:
22	chr5:178306684..178308564-chr5:178323715..178325258,2	MCF-7	breast:
23	chr5:177640785..177642286-chr5:178288319..178291268,2	K562	blood:
24	chr5:178285700..178288538-chr5:178289208..178291375,4	MCF-7	breast:
25	chr5:178286202..178288333-chr5:178295235..178296864,2	MCF-7	breast:
26	chr5:178299499..178302283-chr5:178303072..178304596,2	MCF-7	breast:
27	chr5:178157446..178157947-chr5:178286420..178286940,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF354B-1	chr5:178312615-178312734	NONHSAT105559
2	lnc-ZNF354B-1	chr5:178312488-178312734	NONHSAT105561
3	lnc-ZNF354B-1	chr5:178311168-178311519	NONHSAT105559

No data

Variant related genes	Relation type
ZNF354B	TF binding region
RNU1-39P	TF binding region
ZNF354B	CpG island
RNU1-39P	CpG island
ENSG00000198939	chromatin interactions
ENSG00000177932	chromatin interactions
ENSG00000169131	chromatin interactions
ENSG00000253725	chromatin interactions
ENSG00000178338	chromatin interactions
ENSG00000113240	chromatin interactions

Extended variants
information (count: 2069 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2069 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13157175	chr5:178269682-178269683	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs13180740	chr5:178269685-178269686	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs113792103	chr5:178269692-178269693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs13180861	chr5:178269701-178269702	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs548392000	chr5:178269717-178269718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566637368	chr5:178269722-178269723	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534107903	chr5:178269737-178269738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551858475	chr5:178269744-178269745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570113627	chr5:178269789-178269790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11249596	chr5:178269812-178269813	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs555827987	chr5:178269815-178269816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35862563	chr5:178269819-178269820	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs182764440	chr5:178269862-178269863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374538070	chr5:178269863-178269864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112249524	chr5:178269883-178269884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573426626	chr5:178269898-178269899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186725822	chr5:178269903-178269904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538271547	chr5:178269948-178269949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565087733	chr5:178269953-178269954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146142773	chr5:178269984-178269985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544658915	chr5:178270016-178270017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570988001	chr5:178270044-178270045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562948991	chr5:178270111-178270112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368787380	chr5:178270193-178270194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11743503	chr5:178270194-178270195	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs191577063	chr5:178270208-178270209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568811103	chr5:178270214-178270215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201822164	chr5:178270215-178270216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373456766	chr5:178270243-178270244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552452853	chr5:178270245-178270246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375053188	chr5:178270255-178270256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11249597	chr5:178270274-178270275	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs6885385	chr5:178270311-178270312	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs184899024	chr5:178270313-178270314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549395689	chr5:178270526-178270527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6871777	chr5:178270535-178270536	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs6886989	chr5:178270558-178270559	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs554839113	chr5:178270570-178270571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567058299	chr5:178270581-178270582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11745899	chr5:178270592-178270593	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs374975384	chr5:178270601-178270602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559284450	chr5:178270614-178270615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190192975	chr5:178270679-178270680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs193262426	chr5:178270693-178270694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113959592	chr5:178270699-178270700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527964722	chr5:178270700-178270701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371763754	chr5:178270721-178270722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556613612	chr5:178270746-178270747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs142120002	chr5:178270758-178270759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534059926	chr5:178270776-178270777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1375 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178263600-178286400	Weak transcription	Right Atrium	heart
2	chr5:178266200-178269800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr5:178266400-178281600	Weak transcription	Placenta	Placenta
4	chr5:178272200-178273000	Enhancers	Stomach Smooth Muscle	stomach
5	chr5:178272600-178273200	Enhancers	Fetal Heart	heart
6	chr5:178279400-178279600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:178281400-178281600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:178281400-178281600	Bivalent Enhancer	K562	blood
9	chr5:178281400-178281800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr5:178281400-178281800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:178281600-178281800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:178281600-178281800	Enhancers	K562	blood
13	chr5:178281600-178282000	Enhancers	Placenta	Placenta
14	chr5:178281800-178282400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr5:178282000-178286400	Weak transcription	K562	blood
16	chr5:178282000-178286600	Weak transcription	Placenta	Placenta
17	chr5:178282400-178286600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr5:178284200-178286600	Weak transcription	HSMMtube	muscle
19	chr5:178285800-178286200	Enhancers	HepG2	liver
20	chr5:178285800-178286800	Flanking Active TSS	Dnd41	blood
21	chr5:178286000-178286200	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr5:178286000-178286600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr5:178286000-178287600	Active TSS	Rectal Mucosa Donor 31	rectum
24	chr5:178286000-178288400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr5:178286200-178286400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr5:178286200-178286400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr5:178286200-178286400	Enhancers	Primary T cells from cord blood	blood
28	chr5:178286200-178286400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr5:178286200-178286400	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr5:178286200-178286400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr5:178286200-178286400	Flanking Active TSS	HepG2	liver
32	chr5:178286200-178286400	Enhancers	HMEC	breast
33	chr5:178286200-178286400	Enhancers	HUVEC	blood vessel
34	chr5:178286200-178286600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr5:178286200-178286600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr5:178286200-178286600	Enhancers	Brain Cingulate Gyrus	brain
37	chr5:178286200-178286800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
38	chr5:178286200-178286800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
39	chr5:178286200-178287600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr5:178286200-178287600	Active TSS	Stomach Mucosa	stomach
41	chr5:178286200-178287600	Active TSS	A549	lung
42	chr5:178286200-178287800	Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr5:178286400-178286600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr5:178286400-178286600	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr5:178286400-178286600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr5:178286400-178286600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr5:178286400-178286600	Enhancers	Primary B cells from peripheral blood	blood
48	chr5:178286400-178286600	Active TSS	Primary T cells fromperipheralblood	blood
49	chr5:178286400-178286600	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr5:178286400-178286600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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