Variant report

Variant	nsv1048760
Chromosome Location	chr15:76334544-76496977
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3220)
CpG islands
(count:2506)
Chromatin interactive
region (count:123)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3220 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:76443358-76443550	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:76488758-76489089	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:76483064-76483427	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:76443498-76443553	K562	blood:	n/a	n/a
5	ARID3A	chr15:76478041-76478258	HepG2	liver:	n/a	n/a
6	ATF2	chr15:76473954-76474425	GM12878	blood:	n/a	n/a
7	ATF2	chr15:76483089-76483813	GM12878	blood:	n/a	n/a
8	ATF2	chr15:76473823-76474454	GM12878	blood:	n/a	n/a
9	ATF2	chr15:76349096-76349888	GM12878	blood:	n/a	n/a
10	ATF2	chr15:76443272-76443758	GM12878	blood:	n/a	n/a
11	ATF2	chr15:76443260-76443649	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr15:76461499-76461617	GM12878	blood:	n/a	n/a
13	ATF3	chr15:76461359-76461682	GM12878	blood:	n/a	n/a
14	ATF3	chr15:76461421-76461690	K562	blood:	n/a	n/a
15	ATF3	chr15:76488695-76489271	A549	lung:	n/a	n/a
16	ATF3	chr15:76461375-76461737	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr15:76483297-76483365	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr15:76351387-76352015	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr15:76443332-76443766	GM12878	blood:	n/a	chr15:76443610-76443620
20	BATF	chr15:76427859-76428253	GM12878	blood:	n/a	chr15:76428027-76428038
21	BATF	chr15:76443394-76443743	GM12878	blood:	n/a	chr15:76443610-76443620
22	BATF	chr15:76473865-76474455	GM12878	blood:	n/a	chr15:76474119-76474130
23	BATF	chr15:76349217-76349548	GM12878	blood:	n/a	n/a
24	BATF	chr15:76349194-76349522	GM12878	blood:	n/a	n/a
25	BATF	chr15:76473923-76474319	GM12878	blood:	n/a	chr15:76474119-76474130
26	BCL11A	chr15:76473914-76474363	GM12878	blood:	n/a	n/a
27	BCL11A	chr15:76474032-76474320	GM12878	blood:	n/a	n/a
28	BCL11A	chr15:76349192-76349598	GM12878	blood:	n/a	n/a
29	BCL11A	chr15:76443382-76443708	GM12878	blood:	n/a	n/a
30	BCL11A	chr15:76349275-76349561	GM12878	blood:	n/a	n/a
31	BCL11A	chr15:76443407-76443717	GM12878	blood:	n/a	n/a
32	BCL3	chr15:76488403-76489359	A549	lung:	n/a	n/a
33	BCL3	chr15:76352581-76352897	GM12878	blood:	n/a	chr15:76352840-76352849 chr15:76352720-76352729
34	BCL3	chr15:76349148-76349592	GM12878	blood:	n/a	n/a
35	BCL3	chr15:76351245-76351974	A549	lung:	n/a	n/a
36	BCL3	chr15:76482892-76483810	A549	lung:	n/a	n/a
37	BCLAF1	chr15:76473788-76474517	GM12878	blood:	n/a	n/a
38	BCLAF1	chr15:76473905-76474445	GM12878	blood:	n/a	n/a
39	BCLAF1	chr15:76349196-76350030	GM12878	blood:	n/a	chr15:76349744-76349753
40	BCLAF1	chr15:76443247-76443763	GM12878	blood:	n/a	n/a
41	BHLHE40	chr15:76440299-76440592	GM12878	blood:	n/a	n/a
42	BHLHE40	chr15:76443337-76443588	K562	blood:	n/a	n/a
43	BHLHE40	chr15:76473924-76474330	GM12878	blood:	n/a	n/a
44	BHLHE40	chr15:76486297-76486653	K562	blood:	n/a	n/a
45	BHLHE40	chr15:76488854-76489227	K562	blood:	n/a	n/a
46	BHLHE40	chr15:76443352-76443674	GM12878	blood:	n/a	n/a
47	BHLHE40	chr15:76352447-76353014	GM12878	blood:	n/a	n/a
48	BHLHE40	chr15:76483122-76483431	K562	blood:	n/a	n/a
49	BHLHE40	chr15:76483088-76483437	GM12878	blood:	n/a	n/a
50	BHLHE40	chr15:76375354-76375693	K562	blood:	n/a	chr15:76375519-76375528 chr15:76375519-76375528 chr15:76375518-76375527 chr15:76375517-76375530

(count:2506 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76408398-76408448	U87	brain:	n/a
2	chr15:76440405-76440455	HRCEpiC	kidney:	n/a
3	chr15:76440443-76440493	HUVEC	blood vessel:	n/a
4	chr15:76458372-76458422	AG09319	gingival:	n/a
5	chr15:76496741-76496791	PFSK-1	brain:	n/a
6	chr15:76408398-76408448	U87	brain:	n/a
7	chr15:76440405-76440455	HRCEpiC	kidney:	n/a
8	chr15:76440443-76440493	HUVEC	blood vessel:	n/a
9	chr15:76458372-76458422	AG09319	gingival:	n/a
10	chr15:76496741-76496791	PFSK-1	brain:	n/a
11	chr15:76442477-76442527	SKMC	muscle:	n/a
12	chr15:76483201-76483251	ECC-1	luminal epithelium:	n/a
13	chr15:76408398-76408448	H1-hESC	embryonic stem cell:	embryo
14	chr15:76458279-76458329	HIPEpiC	eye:	n/a
15	chr15:76347846-76347896	MCF10A-Er-Src	breast:	n/a
16	chr15:76461960-76462010	HepG2	liver:	n/a
17	chr15:76461960-76462010	AG10803	skin:	n/a
18	chr15:76351548-76351598	HNPCEpiC	eye:	n/a
19	chr15:76458372-76458422	HIPEpiC	eye:	n/a
20	chr15:76348437-76348487	HCPEpiC	choroid plexus:	n/a
21	chr15:76484379-76484429	HRPEpiC	eye:	n/a
22	chr15:76480434-76480484	HL-60	blood:	n/a
23	chr15:76455848-76455898	K562	blood:	n/a
24	chr15:76429151-76429201	GM12891	blood:	n/a
25	chr15:76408398-76408448	BE2_C	brain:	n/a
26	chr15:76462821-76462871	ProgFib	skin:	n/a
27	chr15:76442477-76442527	AoSMC	blood vessel:	n/a
28	chr15:76484625-76484675	AG09319	gingival:	n/a
29	chr15:76484625-76484675	SK-N-SH_RA	brain:	n/a
30	chr15:76483281-76483331	ovcar-3	ovarian:	n/a
31	chr15:76352047-76352097	SAEC	small airway:	n/a
32	chr15:76458365-76458415	BE2_C	brain:	n/a
33	chr15:76470979-76471029	SK-N-SH	brain:	n/a
34	chr15:76440448-76440498	HCF	heart:	n/a
35	chr15:76352489-76352539	AG04450	lung:	fetal
36	chr15:76352619-76352669	MCF10A-Er-Src	breast:	n/a
37	chr15:76440405-76440455	SK-N-MC	brain:	n/a
38	chr15:76483281-76483331	K562	blood:	n/a
39	chr15:76461960-76462010	IMR90	lung:	fetal
40	chr15:76483344-76483394	T-47D	breast:	n/a
41	chr15:76484473-76484523	MCF10A-Er-Src	breast:	n/a
42	chr15:76442477-76442527	HUVEC	blood vessel:	n/a
43	chr15:76352619-76352669	HUVEC	blood vessel:	n/a
44	chr15:76352619-76352669	PANC-1	pancreas:	n/a
45	chr15:76352532-76352582	GM19239	blood:	n/a
46	chr15:76484379-76484429	AG10803	skin:	n/a
47	chr15:76351442-76351492	NH-A	brain:	n/a
48	chr15:76458279-76458329	Jurkat	blood:	n/a
49	chr15:76480434-76480484	AoSMC	blood vessel:	n/a
50	chr15:76475969-76476019	AG04449	skin:	fetal

(count:123 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:76490388..76492553-chr15:76494551..76496076,2	MCF-7	breast:
2	chr15:76478115..76478633-chr15:76622409..76623267,2	MCF-7	breast:
3	chr15:76435308..76438673-chr15:76443082..76445810,3	K562	blood:
4	chr15:76495383..76497308-chr15:76500785..76502809,2	K562	blood:
5	chr15:76431477..76432448-chr15:76439936..76440516,2	K562	blood:
6	chr15:76355984..76360191-chr15:76360720..76364307,4	K562	blood:
7	chr15:76482924..76483751-chr15:76625816..76626899,5	MCF-7	breast:
8	chr15:76486525..76491130-chr15:76491292..76495169,6	MCF-7	breast:
9	chr15:76472338..76474227-chr15:76482406..76484297,2	K562	blood:
10	chr15:76487953..76490483-chr15:76500123..76503783,3	K562	blood:
11	chr15:76350898..76351807-chr15:76431306..76432503,7	MCF-7	breast:
12	chr15:76484853..76487491-chr15:76488798..76492049,5	K562	blood:
13	chr15:76453448..76455028-chr15:76460465..76463377,2	K562	blood:
14	chr15:76349917..76350459-chr15:76440383..76440942,2	K562	blood:
15	chr15:76455415..76457030-chr15:76460537..76462743,2	K562	blood:
16	chr15:76482840..76483720-chr15:77132911..77133894,4	MCF-7	breast:
17	chr15:76489752..76492594-chr15:76628754..76630476,2	K562	blood:
18	chr15:76349477..76350031-chr15:76443009..76443529,2	K562	blood:
19	chr15:76405575..76406307-chr15:76431978..76432508,2	MCF-7	breast:
20	chr15:76452837..76455028-chr15:76460465..76463193,2	K562	blood:
21	chr15:76398403..76402316-chr15:76403065..76406299,3	K562	blood:
22	chr15:76453204..76454747-chr15:76459797..76461438,2	MCF-7	breast:
23	chr15:76493299..76496201-chr15:76496917..76499323,4	K562	blood:
24	chr15:76341281..76343239-chr15:76349906..76351616,2	MCF-7	breast:
25	chr15:76455415..76457030-chr15:76460537..76462743,2	K562	blood:
26	chr15:76481529..76484202-chr15:76633877..76636476,2	K562	blood:
27	chr15:76483246..76483790-chr15:77158830..77159724,2	K562	blood:
28	chr15:76442105..76446396-chr15:76447199..76450761,5	MCF-7	breast:
29	chr15:76407136..76408714-chr15:76418253..76420251,2	MCF-7	breast:
30	chr15:76460184..76462752-chr15:76465404..76467904,2	K562	blood:
31	chr15:76436435..76439411-chr15:76454805..76456724,2	K562	blood:
32	chr15:76220909..76222483-chr15:76431367..76432547,6	MCF-7	breast:
33	chr15:76452837..76455028-chr15:76460465..76463193,2	K562	blood:
34	chr15:76482740..76483457-chr15:76626133..76626814,2	MCF-7	breast:
35	chr15:76350898..76351807-chr15:76431306..76432503,7	MCF-7	breast:
36	chr15:76353368..76355352-chr15:76428756..76430779,3	MCF-7	breast:
37	chr15:76487373..76491413-chr15:76492592..76495149,4	K562	blood:
38	chr15:76355984..76360191-chr15:76360720..76364307,4	K562	blood:
39	chr15:76460184..76462752-chr15:76465404..76467904,2	K562	blood:
40	chr15:76435308..76437788-chr15:76443138..76445810,3	K562	blood:
41	chr15:76352672..76355541-chr15:76370449..76373002,2	MCF-7	breast:
42	chr15:76348835..76350888-chr15:76431511..76432728,13	MCF-7	breast:
43	chr15:76351996..76354672-chr15:76359589..76362407,2	K562	blood:
44	chr15:76482689..76486583-chr15:76628039..76631365,3	K562	blood:
45	chr15:76483216..76483808-chr15:76625887..76626857,3	K562	blood:
46	chr15:76482420..76485297-chr15:76485451..76488299,2	K562	blood:
47	chr15:76431446..76432246-chr15:76440422..76441109,2	MCF-7	breast:
48	chr15:76461088..76462629-chr15:76483253..76485151,2	K562	blood:
49	chr15:76476723..76478991-chr15:76480313..76482582,2	K562	blood:
50	chr15:76441645..76443484-chr15:76650484..76652153,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXO22-5	chr15:76401374-76401524	NONHSAT047392
2	lnc-FBXO22-5	chr15:76404887-76406544	NONHSAT047392
3	lnc-ETFA-2	chr15:76345279-76345324	NONHSAT047391
4	lnc-ETFA-3	chr15:76336914-76337140	l_1192_chr15:76333969-76337140_testes
5	lnc-ETFA-2	chr15:76349295-76349595	NONHSAT047391
6	lnc-ETFA-2	chr15:76345580-76345710	NONHSAT047391
7	lnc-FBXO22-5	chr15:76404359-76404449	NONHSAT047392
8	lnc-ETFA-2	chr15:76344439-76344518	NONHSAT047391
9	lnc-FBXO22-5	chr15:76352326-76352357	NONHSAT047392

No data

Variant related genes	Relation type
ENSG00000259422	TF binding region
NRG4	TF binding region
C15orf27	TF binding region
ENSG00000259422	CpG island
NRG4	CpG island
C15orf27	CpG island
ENSG00000140367	chromatin interactions
ENSG00000259422	chromatin interactions
ENSG00000270036	chromatin interactions
ENSG00000169758	chromatin interactions
ENSG00000167196	chromatin interactions
ENSG00000114331	chromatin interactions
ENSG00000259514	chromatin interactions
ENSG00000159556	chromatin interactions
ENSG00000140374	chromatin interactions
ENSG00000169752	chromatin interactions

Extended variants
information (count: 5500 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:5500 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551010045	chr15:76334637-76334638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569521074	chr15:76334654-76334655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550196239	chr15:76334714-76334715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191390	chr15:76334718-76334719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs334924	chr15:76334851-76334852	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs539675639	chr15:76334861-76334862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549338923	chr15:76334863-76334864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189038680	chr15:76334875-76334876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115383687	chr15:76334900-76334901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192737640	chr15:76334905-76334906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536331639	chr15:76334974-76334975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559572710	chr15:76334992-76334993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143235082	chr15:76335030-76335031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs334925	chr15:76335031-76335032	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs184735127	chr15:76335041-76335042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577989373	chr15:76335097-76335098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538761041	chr15:76335143-76335144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112925175	chr15:76335183-76335184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147105453	chr15:76335190-76335191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572232641	chr15:76335194-76335195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542706971	chr15:76335217-76335218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138579643	chr15:76335220-76335221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561567986	chr15:76335279-76335280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531769637	chr15:76335290-76335291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143396413	chr15:76335296-76335297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565410692	chr15:76335315-76335316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113003167	chr15:76335343-76335344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34741213	chr15:76335376-76335377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189640468	chr15:76335531-76335532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529864014	chr15:76335551-76335552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs168029	chr15:76336942-76336943	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs190320951	chr15:76336992-76336993	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs571949445	chr15:76336993-76336994	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs530569787	chr15:76337004-76337005	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs545877502	chr15:76337009-76337010	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs540785343	chr15:76337033-76337034	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs557394024	chr15:76345302-76345303	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs114139605	chr15:76345600-76345601	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs547000239	chr15:76345601-76345602	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs528068563	chr15:76345677-76345678	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs190260221	chr15:76346258-76346259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548410628	chr15:76346279-76346280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191463033	chr15:76346287-76346288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570190633	chr15:76346318-76346319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150310175	chr15:76346319-76346320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552844313	chr15:76346379-76346380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571016407	chr15:76346391-76346392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs137932312	chr15:76346453-76346454	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs369089679	chr15:76346521-76346522	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs185368963	chr15:76346576-76346577	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Intellectual disability	22102821	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
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21611746	CNVD

Chromatin state (count:2809 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76331600-76335600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr15:76346200-76346400	Enhancers	Hela-S3	cervix
3	chr15:76346400-76346600	Flanking Active TSS	Hela-S3	cervix
4	chr15:76346600-76347000	Active TSS	Hela-S3	cervix
5	chr15:76347000-76349000	Weak transcription	Hela-S3	cervix
6	chr15:76348400-76350000	Enhancers	Primary B cells from peripheral blood	blood
7	chr15:76348800-76349000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr15:76348800-76349000	Enhancers	GM12878-XiMat	blood
9	chr15:76348800-76349000	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr15:76348800-76349200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr15:76348800-76349600	Enhancers	Primary B cells from cord blood	blood
12	chr15:76348800-76349600	Enhancers	Primary hematopoietic stem cells	blood
13	chr15:76349000-76349200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr15:76349000-76349400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr15:76349000-76349400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr15:76349000-76349400	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr15:76349000-76349400	Enhancers	Hela-S3	cervix
18	chr15:76349000-76349600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr15:76349000-76349600	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr15:76349000-76349600	Enhancers	HMEC	breast
21	chr15:76349000-76349600	Enhancers	NHEK	skin
22	chr15:76349000-76349800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr15:76349000-76349800	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr15:76349000-76350000	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr15:76349000-76350000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr15:76349000-76350000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr15:76349000-76350000	Flanking Active TSS	GM12878-XiMat	blood
28	chr15:76349000-76350000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr15:76349200-76349400	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr15:76349200-76349400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr15:76349200-76349600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr15:76349200-76349600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr15:76349200-76349600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr15:76349200-76349600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr15:76349200-76349600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr15:76349200-76349600	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr15:76349200-76349600	Enhancers	Brain Anterior Caudate	brain
38	chr15:76349200-76349600	Enhancers	Placenta Amnion	Placenta Amnion
39	chr15:76349200-76349600	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr15:76349200-76349600	Enhancers	Stomach Mucosa	stomach
41	chr15:76349200-76349600	Bivalent Enhancer	A549	lung
42	chr15:76349200-76349800	Enhancers	H1 Cell Line	embryonic stem cell
43	chr15:76349200-76349800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr15:76349200-76350000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr15:76349200-76350000	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr15:76349200-76350000	Enhancers	Primary T cells from cord blood	blood
47	chr15:76349200-76350000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
48	chr15:76349200-76350000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr15:76349400-76349600	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
50	chr15:76349400-76349600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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