Variant report

Variant	esv20801
Chromosome Location	chr15:99644218-99646022
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	ATF3	chr15:99644815-99645555	A549	lung:	n/a	chr15:99645174-99645183 chr15:99645241-99645250
2	BACH1	chr15:99644980-99645179	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr15:99645817-99646529	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr15:99644781-99645678	A549	lung:	n/a	chr15:99645154-99645162 chr15:99645148-99645161 chr15:99645299-99645312 chr15:99645370-99645383
5	BHLHE40	chr15:99645130-99645138	K562	blood:	n/a	n/a
6	BRCA1	chr15:99645141-99645387	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr15:99645083-99645283	HepG2	liver:	n/a	n/a
8	CCNT2	chr15:99645068-99645824	K562	blood:	n/a	n/a
9	CEBPB	chr15:99645038-99645173	HepG2	liver:	n/a	n/a
10	CEBPB	chr15:99644974-99645221	Hela-S3	cervix:	n/a	chr15:99645194-99645202
11	CEBPD	chr15:99645199-99645374	HepG2	liver:	n/a	n/a
12	CEBPD	chr15:99644969-99645494	HepG2	liver:	n/a	n/a
13	CHD1	chr15:99645905-99645962	GM12878	blood:	n/a	n/a
14	CHD2	chr15:99645342-99645540	HepG2	liver:	n/a	n/a
15	CHD2	chr15:99644990-99645240	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr15:99644994-99645617	Hela-S3	cervix:	n/a	chr15:99645239-99645249
17	CHD2	chr15:99645825-99646089	Hela-S3	cervix:	n/a	n/a
18	CREB1	chr15:99644870-99646275	A549	lung:	n/a	n/a
19	CREB1	chr15:99644958-99645414	A549	lung:	n/a	n/a
20	CTBP2	chr15:99645816-99646328	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr15:99645900-99646050	HFF-Myc	foreskin:	n/a	n/a
22	CTCF	chr15:99644979-99645261	H1-hESC	embryonic stem cell:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
23	CTCF	chr15:99645960-99646110	GM12871	blood:	n/a	n/a
24	CTCF	chr15:99645040-99645190	HepG2	liver:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
25	CTCF	chr15:99644989-99645279	GM19240	blood:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
26	CTCF	chr15:99644979-99644980	GM13977	blood:	n/a	n/a
27	CTCF	chr15:99644968-99645281	GM19238	blood:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
28	CTCF	chr15:99645640-99645790	SAEC	small airway:	n/a	n/a
29	CTCF	chr15:99645080-99645230	HAc	cerebellar:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
30	CTCF	chr15:99645020-99645170	AG10803	skin:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
31	CTCF	chr15:99645060-99645210	GM12869	blood:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
32	CTCF	chr15:99645621-99645849	GM19239	blood:	n/a	n/a
33	CTCF	chr15:99644973-99645255	MCF-7	breast:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
34	CTCF	chr15:99645887-99646158	NHEK	skin:	n/a	n/a
35	CTCF	chr15:99645680-99645830	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr15:99644975-99645304	K562	blood:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
37	CTCF	chr15:99646020-99646170	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr15:99644982-99645282	Gliobla	brain:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
39	CTCF	chr15:99646020-99646170	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr15:99645900-99646050	AG09319	gingival:	n/a	n/a
41	CTCF	chr15:99645060-99645210	HUVEC	blood vessel:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
42	CTCF	chr15:99644964-99645278	A549	lung:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
43	CTCF	chr15:99645080-99645230	HMEC	breast:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
44	CTCF	chr15:99645040-99645190	GM12869	blood:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
45	CTCF	chr15:99645000-99645150	A549	lung:	n/a	chr15:99645126-99645139
46	CTCF	chr15:99645940-99646090	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr15:99644980-99645130	AG04450	lung:	n/a	n/a
48	CTCF	chr15:99645080-99645230	HA-sp	spinal cord:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
49	CTCF	chr15:99645040-99645190	Caco-2	colon:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
50	CTCF	chr15:99645940-99646090	HA-sp	spinal cord:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:99645088-99645138	HAEpiC	amniotic membrane:	n/a
2	chr15:99645088-99645138	HAEpiC	amniotic membrane:	n/a
3	chr15:99645065-99645115	HAEpiC	amniotic membrane:	n/a
4	chr15:99645227-99645277	PANC-1	pancreas:	n/a
5	chr15:99645435-99645485	HEK293	kidney:	embryo
6	chr15:99645088-99645138	BJ	skin:	n/a
7	chr15:99645065-99645115	HRPEpiC	eye:	n/a
8	chr15:99645088-99645138	HMEC	breast:	n/a
9	chr15:99645435-99645485	HPAEpiC	pulmonary alveolar:	n/a
10	chr15:99645231-99645281	HRCEpiC	kidney:	n/a
11	chr15:99645065-99645115	MCF10A-Er-Src	breast:	n/a
12	chr15:99645096-99645146	HepG2	liver:	n/a
13	chr15:99644973-99645023	Hepatocyte	liver:	n/a
14	chr15:99645435-99645485	Caco-2	colon:	n/a
15	chr15:99645435-99645485	LNCaP	prostate:	n/a
16	chr15:99645031-99645081	GM12878	blood:	n/a
17	chr15:99645435-99645485	NHDF-neo	bronchial:	n/a
18	chr15:99644973-99645023	RPTEC	kidney:	n/a
19	chr15:99645065-99645115	SK-N-SH	brain:	n/a
20	chr15:99645663-99645713	SK-N-MC	brain:	n/a
21	chr15:99645096-99645146	PrEC	prostate:	n/a
22	chr15:99644973-99645023	AG10803	skin:	n/a
23	chr15:99645031-99645081	AoSMC	blood vessel:	n/a
24	chr15:99645435-99645485	GM12878	blood:	n/a
25	chr15:99645065-99645115	AG09319	gingival:	n/a
26	chr15:99645096-99645146	HRCEpiC	kidney:	n/a
27	chr15:99645031-99645081	SK-N-SH	brain:	n/a
28	chr15:99645663-99645713	Hepatocyte	liver:	n/a
29	chr15:99645663-99645713	AG09309	skin:	n/a
30	chr15:99645663-99645713	NB4	blood:	n/a
31	chr15:99645096-99645146	CMK	blood:	n/a
32	chr15:99645065-99645115	PANC-1	pancreas:	n/a
33	chr15:99644973-99645023	HL-60	blood:	n/a
34	chr15:99645227-99645277	AG04449	skin:	fetal
35	chr15:99645231-99645281	BE2_C	brain:	n/a
36	chr15:99645065-99645115	AG04449	skin:	fetal
37	chr15:99645096-99645146	BJ	skin:	n/a
38	chr15:99645096-99645146	IMR90	lung:	fetal
39	chr15:99645227-99645277	NT2-D1	testis:	n/a
40	chr15:99645227-99645277	GM12891	blood:	n/a
41	chr15:99645065-99645115	IMR90	lung:	fetal
42	chr15:99645096-99645146	SK-N-SH_RA	brain:	n/a
43	chr15:99645088-99645138	HIPEpiC	eye:	n/a
44	chr15:99645435-99645485	HIPEpiC	eye:	n/a
45	chr15:99645435-99645485	SK-N-MC	brain:	n/a
46	chr15:99644973-99645023	AG04450	lung:	fetal
47	chr15:99645227-99645277	PrEC	prostate:	n/a
48	chr15:99645096-99645146	U87	brain:	n/a
49	chr15:99645065-99645115	NB4	blood:	n/a
50	chr15:99645088-99645138	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:99645187..99645735-chr5:79703316..79703974,2	Hela-S3	cervix:
2	chr15:99643812..99646594-chr15:99789555..99792592,4	MCF-7	breast:
3	chr15:99644709..99645388-chr15:99791744..99792284,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PGPEP1L-1	chr15:99645894-99646030	ENSG00000259475.1

Variant related genes	Relation type
SYNM	TF binding region
SYNM	CpG island
ENSG00000168904	chromatin interactions
ENSG00000039319	chromatin interactions
ENSG00000103852	chromatin interactions

Extended variants
information (count: 77 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:77 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12440983	chr15:99644259-99644260	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140244636	chr15:99644278-99644279	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs544459768	chr15:99644285-99644286	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs372182813	chr15:99644287-99644288	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs563134737	chr15:99644300-99644301	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs145535406	chr15:99644316-99644317	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs12441605	chr15:99644354-99644355	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs371328103	chr15:99644362-99644363	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs59003596	chr15:99644363-99644364	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs75343220	chr15:99644394-99644395	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs78026504	chr15:99644396-99644397	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs560363566	chr15:99644429-99644430	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs545762894	chr15:99644436-99644437	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs560478946	chr15:99644476-99644477	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs527696926	chr15:99644486-99644487	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs112390436	chr15:99644512-99644513	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs529616979	chr15:99644545-99644546	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs112666378	chr15:99644605-99644606	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
19	rs143156196	chr15:99644609-99644610	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs550486000	chr15:99644715-99644716	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs8029240	chr15:99644735-99644736	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs191385029	chr15:99644750-99644751	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs182637319	chr15:99644752-99644753	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs371486888	chr15:99644760-99644761	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs28673457	chr15:99644786-99644787	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs8028199	chr15:99644796-99644797	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs539342178	chr15:99644827-99644828	Weak transcription Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs8028233	chr15:99644844-99644845	Weak transcription Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs201786843	chr15:99644867-99644868	Weak transcription Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs112113914	chr15:99644871-99644872	Weak transcription Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs533565757	chr15:99644883-99644884	Weak transcription Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs12324621	chr15:99644930-99644931	Weak transcription Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs116586728	chr15:99644991-99644992	Weak transcription Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs537988909	chr15:99645057-99645058	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs556477841	chr15:99645103-99645104	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs578127010	chr15:99645165-99645166	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs529448439	chr15:99645205-99645206	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs371526816	chr15:99645229-99645230	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs560784668	chr15:99645241-99645242	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs572442074	chr15:99645249-99645250	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs34878632	chr15:99645262-99645263	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs368473966	chr15:99645289-99645290	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs561365359	chr15:99645304-99645305	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs147489374	chr15:99645308-99645309	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs532137659	chr15:99645311-99645312	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs139850386	chr15:99645348-99645349	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs368523854	chr15:99645361-99645362	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs369166722	chr15:99645374-99645375	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs532969217	chr15:99645382-99645383	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs551225973	chr15:99645428-99645429	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Intellectual disability	22102821	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	21147756	CNVD
Hepatocellular carcinoma	16750200	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	20811773	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Emphysema	19352772	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Prostate cancer	18632612	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:99640800-99645000	Weak transcription	Pancreas	Pancrea
2	chr15:99641000-99644800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr15:99641000-99645000	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr15:99641000-99645000	Weak transcription	Right Ventricle	heart
5	chr15:99641000-99645200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr15:99641000-99645200	Weak transcription	Gastric	stomach
7	chr15:99641200-99644800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr15:99641200-99644800	Weak transcription	Stomach Smooth Muscle	stomach
9	chr15:99641200-99645200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr15:99641200-99645200	Weak transcription	Colon Smooth Muscle	Colon
11	chr15:99641200-99645400	Weak transcription	Brain Substantia Nigra	brain
12	chr15:99643000-99645200	Weak transcription	A549	lung
13	chr15:99643400-99645000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr15:99643400-99645200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr15:99643600-99645000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr15:99643800-99645000	Weak transcription	Adipose Nuclei	Adipose
17	chr15:99643800-99645000	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr15:99643800-99645200	Weak transcription	Psoas Muscle	Psoas
19	chr15:99644000-99645200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr15:99644800-99645000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr15:99644800-99645000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr15:99644800-99645000	Bivalent/Poised TSS	Colonic Mucosa	Colon
23	chr15:99644800-99645200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr15:99644800-99645200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
25	chr15:99644800-99645200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr15:99644800-99645200	Bivalent Enhancer	Fetal Thymus	thymus
27	chr15:99644800-99645400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
28	chr15:99644800-99645600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr15:99644800-99646000	Active TSS	Stomach Smooth Muscle	stomach
30	chr15:99644800-99646000	Active TSS	HepG2	liver
31	chr15:99644800-99646200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr15:99644800-99646200	Enhancers	Liver	Liver
33	chr15:99644800-99646200	Active TSS	Hela-S3	cervix
34	chr15:99644800-99646400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr15:99644800-99646600	Active TSS	NHLF	lung
36	chr15:99644800-99646600	Active TSS	Osteobl	bone
37	chr15:99644800-99646800	Active TSS	Brain Angular Gyrus	brain
38	chr15:99644800-99647200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr15:99645000-99645200	Enhancers	Primary B cells from cord blood	blood
40	chr15:99645000-99645200	Enhancers	Primary T cells from cord blood	blood
41	chr15:99645000-99645200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
42	chr15:99645000-99645200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr15:99645000-99645200	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
44	chr15:99645000-99645200	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr15:99645000-99645200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr15:99645000-99645200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr15:99645000-99645200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr15:99645000-99645200	Flanking Bivalent TSS/Enh	Primary mononuclear cells fromperipheralblood	Blood
49	chr15:99645000-99645200	Active TSS	Adipose Nuclei	Adipose
50	chr15:99645000-99645200	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain

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