Variant report

Variant	esv1845471
Chromosome Location	chr15:54556063-54685463
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:478)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr15:54590571-54590953	GM12878	blood:	n/a	n/a
2	ATF2	chr15:54581644-54582480	GM12878	blood:	n/a	chr15:54582279-54582286
3	ATF2	chr15:54639602-54640105	GM12878	blood:	n/a	n/a
4	ATF2	chr15:54599289-54599751	GM12878	blood:	n/a	n/a
5	ATF2	chr15:54581634-54582493	GM12878	blood:	n/a	chr15:54582279-54582286
6	ATF2	chr15:54599386-54599772	GM12878	blood:	n/a	n/a
7	ATF2	chr15:54639572-54640054	GM12878	blood:	n/a	n/a
8	ATF2	chr15:54580208-54580569	GM12878	blood:	n/a	n/a
9	BACH1	chr15:54588100-54588108	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr15:54581823-54582317	GM12878	blood:	n/a	n/a
11	BATF	chr15:54580237-54580630	GM12878	blood:	n/a	n/a
12	BATF	chr15:54599821-54600121	GM12878	blood:	n/a	n/a
13	BATF	chr15:54599372-54599768	GM12878	blood:	n/a	n/a
14	BATF	chr15:54600209-54600425	GM12878	blood:	n/a	chr15:54600321-54600330
15	BATF	chr15:54590632-54591001	GM12878	blood:	n/a	n/a
16	BATF	chr15:54639665-54640035	GM12878	blood:	n/a	chr15:54639830-54639839
17	BATF	chr15:54639669-54639952	GM12878	blood:	n/a	chr15:54639830-54639839
18	BATF	chr15:54581748-54582453	GM12878	blood:	n/a	n/a
19	BCL11A	chr15:54581857-54582369	GM12878	blood:	n/a	n/a
20	BCL11A	chr15:54599485-54599711	GM12878	blood:	n/a	n/a
21	BCL11A	chr15:54639707-54639892	GM12878	blood:	n/a	n/a
22	BCL11A	chr15:54590664-54590952	GM12878	blood:	n/a	n/a
23	BCL11A	chr15:54599364-54599814	GM12878	blood:	n/a	n/a
24	BCL11A	chr15:54581737-54582398	GM12878	blood:	n/a	n/a
25	BCL11A	chr15:54590590-54590994	GM12878	blood:	n/a	n/a
26	BCL11A	chr15:54639645-54639975	GM12878	blood:	n/a	n/a
27	BCL11A	chr15:54600164-54600441	GM12878	blood:	n/a	n/a
28	BCL11A	chr15:54580252-54580540	GM12878	blood:	n/a	n/a
29	BCL3	chr15:54581775-54582362	GM12878	blood:	n/a	n/a
30	BCL3	chr15:54639618-54640100	GM12878	blood:	n/a	chr15:54640025-54640034
31	BCLAF1	chr15:54639648-54640034	GM12878	blood:	n/a	chr15:54640025-54640034
32	BCLAF1	chr15:54590619-54590970	GM12878	blood:	n/a	n/a
33	BHLHE40	chr15:54600053-54600525	GM12878	blood:	n/a	n/a
34	BHLHE40	chr15:54590309-54591338	GM12878	blood:	n/a	n/a
35	BHLHE40	chr15:54638217-54638393	GM12878	blood:	n/a	n/a
36	BHLHE40	chr15:54599536-54599786	GM12878	blood:	n/a	n/a
37	BHLHE40	chr15:54639443-54640056	GM12878	blood:	n/a	n/a
38	BHLHE40	chr15:54581809-54582435	GM12878	blood:	n/a	n/a
39	CEBPB	chr15:54570799-54571094	HepG2	liver:	n/a	n/a
40	CEBPB	chr15:54581889-54582413	GM12878	blood:	n/a	n/a
41	CEBPB	chr15:54599420-54599863	GM12878	blood:	n/a	n/a
42	CEBPB	chr15:54558308-54558550	HepG2	liver:	n/a	n/a
43	CEBPB	chr15:54582243-54582443	HepG2	liver:	n/a	n/a
44	CHD1	chr15:54639830-54639977	GM12878	blood:	n/a	n/a
45	CHD1	chr15:54590445-54590920	GM12878	blood:	n/a	n/a
46	CHD1	chr15:54580510-54580866	GM12878	blood:	n/a	n/a
47	CHD2	chr15:54599559-54599774	GM12878	blood:	n/a	n/a
48	CHD2	chr15:54683226-54683274	GM12878	blood:	n/a	n/a
49	CHD2	chr15:54638152-54638373	GM12878	blood:	n/a	n/a
50	CHD2	chr15:54590662-54591020	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:54638342-54638392	NHDF-neo	bronchial:	n/a
2	chr15:54582445-54582495	GM12892	blood:	n/a
3	chr15:54582445-54582495	K562	blood:	n/a
4	chr15:54582445-54582495	PFSK-1	brain:	n/a
5	chr15:54638342-54638392	SKMC	muscle:	n/a
6	chr15:54582445-54582495	SAEC	small airway:	n/a
7	chr15:54638342-54638392	LNCaP	prostate:	n/a
8	chr15:54638342-54638392	T-47D	breast:	n/a
9	chr15:54582445-54582495	CMK	blood:	n/a
10	chr15:54582445-54582495	HL-60	blood:	n/a
11	chr15:54582445-54582495	AG09309	skin:	n/a
12	chr15:54638342-54638392	AG10803	skin:	n/a
13	chr15:54582445-54582495	MCF10A-Er-Src	breast:	n/a
14	chr15:54638342-54638392	HEEpiC	esophagus:	n/a
15	chr15:54638342-54638392	U87	brain:	n/a
16	chr15:54582445-54582495	HUVEC	blood vessel:	n/a
17	chr15:54582445-54582495	AG04450	lung:	fetal
18	chr15:54638342-54638392	PANC-1	pancreas:	n/a
19	chr15:54638342-54638392	Hela-S3	cervix:	n/a
20	chr15:54638342-54638392	BE2_C	brain:	n/a
21	chr15:54638342-54638392	IMR90	lung:	fetal
22	chr15:54638342-54638392	Caco-2	colon:	n/a
23	chr15:54638342-54638392	ovcar-3	ovarian:	n/a
24	chr15:54582445-54582495	IMR90	lung:	fetal
25	chr15:54582445-54582495	HCF	heart:	n/a
26	chr15:54582445-54582495	NB4	blood:	n/a
27	chr15:54582445-54582495	SK-N-SH	brain:	n/a
28	chr15:54582445-54582495	HEEpiC	esophagus:	n/a
29	chr15:54582445-54582495	HCT-116	colon:	n/a
30	chr15:54582445-54582495	H1-hESC	embryonic stem cell:	embryo
31	chr15:54582445-54582495	HepG2	liver:	n/a
32	chr15:54582445-54582495	LNCaP	prostate:	n/a
33	chr15:54638342-54638392	BJ	skin:	n/a
34	chr15:54582445-54582495	PrEC	prostate:	n/a
35	chr15:54638342-54638392	MCF-7	breast:	n/a
36	chr15:54582445-54582495	AG10803	skin:	n/a
37	chr15:54582445-54582495	HRE	kidney:	n/a
38	chr15:54638342-54638392	Hepatocyte	liver:	n/a
39	chr15:54638342-54638392	A549	lung:	n/a
40	chr15:54638342-54638392	HEK293	kidney:	embryo
41	chr15:54582445-54582495	AG04449	skin:	fetal
42	chr15:54582445-54582495	SK-N-MC	brain:	n/a
43	chr15:54638342-54638392	GM12878	blood:	n/a
44	chr15:54638342-54638392	NT2-D1	testis:	n/a
45	chr15:54582445-54582495	AG09319	gingival:	n/a
46	chr15:54638342-54638392	AoSMC	blood vessel:	n/a
47	chr15:54582445-54582495	Hela-S3	cervix:	n/a
48	chr15:54638342-54638392	HPAEpiC	pulmonary alveolar:	n/a
49	chr15:54582445-54582495	NHDF-neo	bronchial:	n/a
50	chr15:54582445-54582495	NT2-D1	testis:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:54593390..54595491-chr15:54595837..54597539,2	MCF-7	breast:
2	chr15:54468684..54471121-chr15:54610190..54612096,2	K562	blood:
3	chr10:66995726..66996297-chr15:54670543..54671043,2	NB4	blood:
4	chr15:54593390..54595491-chr15:54595837..54597539,2	MCF-7	breast:
5	chr15:54685449..54687612-chr15:54692436..54693986,2	K562	blood:
6	chr15:54627743..54629757-chr15:54746231..54748915,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR72-6	chr15:54684866-54684973	ucscGeneNc_uc002ads_2
2	lnc-WDR72-6	chr15:54623049-54623302	ucscGeneNc_uc002ads_2
3	lnc-WDR72-6	chr15:54628647-54629000	ucscGeneNc_uc002ads_2
4	lnc-WDR72-6	chr15:54627937-54628091	ucscGeneNc_uc002ads_2
5	lnc-WDR72-6	chr15:54627350-54627497	ucscGeneNc_uc002ads_2
6	lnc-WDR72-6	chr15:54672210-54672342	ucscGeneNc_uc002ads_2
7	lnc-WDR72-5	chr15:54612929-54613763	NONHSAT043975
8	lnc-WDR72-6	chr15:54622446-54622586	ucscGeneNc_uc002ads_2
9	lnc-WDR72-6	chr15:54683330-54683361	ucscGeneNc_uc002ads_2

No data

Variant related genes	Relation type
HNRNPA1P74	TF binding region
UNC13C	TF binding region
HNRNPA1P74	CpG island
UNC13C	CpG island

Extended variants
information (count: 4758 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4758 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12917198	chr15:54556063-54556064	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185737893	chr15:54556080-54556081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189867439	chr15:54556124-54556125	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs74670077	chr15:54556133-54556134	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs377673320	chr15:54556139-54556140	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs369128305	chr15:54556143-54556144	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs539597364	chr15:54556166-54556167	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs74013568	chr15:54556189-54556190	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs114566070	chr15:54556244-54556245	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs12917364	chr15:54556259-54556260	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs117178466	chr15:54556270-54556271	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs138053712	chr15:54556292-54556293	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs368687026	chr15:54556298-54556299	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs76795278	chr15:54556332-54556333	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs557176265	chr15:54556370-54556371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577123144	chr15:54556388-54556389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201440683	chr15:54556398-54556399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565769380	chr15:54556439-54556440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376965914	chr15:54556455-54556456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536522542	chr15:54556542-54556543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192038263	chr15:54556630-54556631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535441398	chr15:54556673-54556674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545520801	chr15:54556674-54556675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7164366	chr15:54556718-54556719	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs138753964	chr15:54556742-54556743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542274793	chr15:54556794-54556795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575759880	chr15:54556822-54556823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200173884	chr15:54556824-54556825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557731335	chr15:54556834-54556835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561953492	chr15:54556852-54556853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530906026	chr15:54556878-54556879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577493157	chr15:54556881-54556882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564759333	chr15:54556913-54556914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533395730	chr15:54556941-54556942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555467373	chr15:54556981-54556982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142541996	chr15:54556985-54556986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541692291	chr15:54556992-54556993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs5025252	chr15:54557102-54557103	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs530250639	chr15:54557239-54557240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534555494	chr15:54557258-54557259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184488010	chr15:54557260-54557261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74397078	chr15:54557267-54557268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35133346	chr15:54557276-54557277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537012749	chr15:54557382-54557383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs117235401	chr15:54557442-54557443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577205554	chr15:54557456-54557457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539670210	chr15:54557465-54557466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34610472	chr15:54557490-54557491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs79567943	chr15:54557517-54557518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs117555253	chr15:54557520-54557521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	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
Colorectal cancer	16774939	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
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:54547000-54652600	Weak transcription	Fetal Lung	lung
2	chr15:54556200-54556400	Enhancers	Aorta	Aorta
3	chr15:54569400-54571400	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr15:54570200-54570800	Enhancers	Aorta	Aorta
5	chr15:54570800-54571200	Weak transcription	Aorta	Aorta
6	chr15:54570800-54571600	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr15:54571200-54571800	Enhancers	Aorta	Aorta
8	chr15:54571400-54571800	Enhancers	Adipose Nuclei	Adipose
9	chr15:54580200-54580800	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr15:54580200-54581200	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr15:54592600-54593000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr15:54593000-54596600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr15:54596200-54598000	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr15:54596600-54598400	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr15:54602600-54602800	Enhancers	Aorta	Aorta
16	chr15:54602800-54638000	Weak transcription	Aorta	Aorta
17	chr15:54604600-54605200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr15:54604600-54605400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr15:54604800-54605200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr15:54604800-54605200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr15:54604800-54605400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr15:54604800-54605600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr15:54609600-54610600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr15:54611600-54614400	Enhancers	Fetal Brain Female	brain
25	chr15:54612800-54613400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr15:54613200-54614000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr15:54613200-54614800	Enhancers	Brain Germinal Matrix	brain
28	chr15:54613400-54616000	Enhancers	Fetal Brain Male	brain
29	chr15:54614400-54615600	Weak transcription	Fetal Brain Female	brain
30	chr15:54614600-54614800	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr15:54614800-54617400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr15:54615800-54616000	Enhancers	Fetal Brain Female	brain
33	chr15:54616000-54619400	Weak transcription	Fetal Brain Male	brain
34	chr15:54617000-54618200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr15:54617200-54617400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr15:54617200-54617400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr15:54617400-54617600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr15:54617400-54618000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr15:54617400-54618200	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr15:54617400-54618200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr15:54617400-54620200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr15:54617600-54618200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr15:54618000-54618800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr15:54618000-54619000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr15:54618000-54619000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr15:54618200-54618400	Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr15:54618200-54618400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
48	chr15:54618200-54618400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr15:54618200-54618600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr15:54618200-54618600	Active TSS	iPS-20b Cell Line	embryonic stem cell

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