Variant report

Variant	nsv904112
Chromosome Location	chr15:41806658-41836234
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:514)
CpG islands
(count:244)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:514 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:41810295-41810629	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:41827866-41828096	K562	blood:	n/a	n/a
3	ARID3A	chr15:41836215-41836598	HepG2	liver:	n/a	n/a
4	ATF2	chr15:41836140-41836632	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr15:41836011-41836700	K562	blood:	n/a	n/a
6	BRCA1	chr15:41836153-41836511	HepG2	liver:	n/a	n/a
7	CBX3	chr15:41836188-41836759	K562	blood:	n/a	n/a
8	CCNT2	chr15:41836164-41836665	K562	blood:	n/a	n/a
9	CEBPB	chr15:41829444-41829466	HepG2	liver:	n/a	chr15:41829451-41829462
10	CEBPB	chr15:41836111-41837158	Hela-S3	cervix:	n/a	n/a
11	CEBPD	chr15:41836115-41836704	HepG2	liver:	n/a	n/a
12	CEBPD	chr15:41836204-41836798	K562	blood:	n/a	chr15:41836703-41836714
13	CHD2	chr15:41836211-41836574	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr15:41810343-41810521	HepG2	liver:	n/a	n/a
15	CHD2	chr15:41836060-41836612	GM12878	blood:	n/a	n/a
16	CREB1	chr15:41810116-41810666	HepG2	liver:	n/a	n/a
17	CREB1	chr15:41836140-41836648	A549	lung:	n/a	n/a
18	CTCF	chr15:41814064-41814075	Spleen_OC	spleen:	n/a	n/a
19	CTCF	chr15:41822740-41822890	BE2_C	brain:	n/a	n/a
20	CTCF	chr15:41836160-41836310	SK-N-SH_RA	brain:	n/a	n/a
21	CUX1	chr15:41806439-41806784	K562	blood:	n/a	chr15:41806648-41806657 chr15:41806648-41806657
22	ELF1	chr15:41836103-41836720	GM12878	blood:	n/a	chr15:41836470-41836479
23	ELF1	chr15:41836135-41836622	HepG2	liver:	n/a	chr15:41836470-41836479
24	ELF1	chr15:41836126-41836693	HepG2	liver:	n/a	chr15:41836470-41836479
25	ELF1	chr15:41836214-41836720	MCF-7	breast:	n/a	chr15:41836470-41836479
26	ELF1	chr15:41836049-41836716	GM12878	blood:	n/a	chr15:41836470-41836479
27	ELF1	chr15:41836060-41836716	K562	blood:	n/a	chr15:41836470-41836479
28	ELF1	chr15:41836227-41836693	K562	blood:	n/a	chr15:41836470-41836479
29	ELF1	chr15:41836217-41836656	MCF-7	breast:	n/a	chr15:41836470-41836479
30	ELF1	chr15:41836150-41836736	SK-N-SH	brain:	n/a	chr15:41836470-41836479
31	ELK1	chr15:41836181-41836627	Hela-S3	cervix:	n/a	n/a
32	ELK4	chr15:41836012-41836576	Hela-S3	cervix:	n/a	n/a
33	EP300	chr15:41836212-41836417	HepG2	liver:	n/a	n/a
34	EP300	chr15:41827861-41828055	K562	blood:	n/a	n/a
35	EP300	chr15:41836180-41836629	ECC-1	luminal epithelium:	n/a	n/a
36	EP300	chr15:41810358-41810509	HepG2	liver:	n/a	n/a
37	EP300	chr15:41822080-41823482	SK-N-SH	brain:	n/a	n/a
38	EP300	chr15:41836081-41836747	ECC-1	luminal epithelium:	n/a	n/a
39	EP300	chr15:41822448-41823266	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr15:41835248-41835312	K562	blood:	n/a	n/a
41	EP300	chr15:41822492-41823250	SK-N-SH_RA	brain:	n/a	n/a
42	ETS1	chr15:41836027-41836689	GM12878	blood:	n/a	chr15:41836507-41836520 chr15:41836470-41836481
43	ETS1	chr15:41836072-41836612	K562	blood:	n/a	chr15:41836507-41836520 chr15:41836470-41836481
44	ETS1	chr15:41836186-41836626	K562	blood:	n/a	chr15:41836507-41836520 chr15:41836470-41836481
45	ETS1	chr15:41836160-41836639	GM12878	blood:	n/a	chr15:41836507-41836520 chr15:41836470-41836481
46	ETS1	chr15:41836200-41836695	A549	lung:	n/a	chr15:41836507-41836520 chr15:41836470-41836481
47	FOS	chr15:41836109-41836219	MCF10A-Er-Src	breast:	n/a	n/a
48	FOXA1	chr15:41810196-41810583	HepG2	liver:	n/a	n/a
49	FOXA1	chr15:41810174-41810662	HepG2	liver:	n/a	n/a
50	FOXA1	chr15:41810174-41810643	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:41806867-41806917	HCF	heart:	n/a
2	chr15:41832778-41832828	GM06990	blood:	n/a
3	chr15:41820721-41820771	K562	blood:	n/a
4	chr15:41836038-41836088	MCF10A-Er-Src	breast:	n/a
5	chr15:41820721-41820771	HEK293	kidney:	embryo
6	chr15:41836038-41836088	ProgFib	skin:	n/a
7	chr15:41832778-41832828	HIPEpiC	eye:	n/a
8	chr15:41806867-41806917	SK-N-SH_RA	brain:	n/a
9	chr15:41832778-41832828	HCF	heart:	n/a
10	chr15:41836038-41836088	HNPCEpiC	eye:	n/a
11	chr15:41836038-41836088	MCF-7	breast:	n/a
12	chr15:41836038-41836088	T-47D	breast:	n/a
13	chr15:41836038-41836088	SK-N-SH_RA	brain:	n/a
14	chr15:41820721-41820771	HepG2	liver:	n/a
15	chr15:41806867-41806917	RPTEC	kidney:	n/a
16	chr15:41806867-41806917	PrEC	prostate:	n/a
17	chr15:41836038-41836088	HRCEpiC	kidney:	n/a
18	chr15:41820721-41820771	Caco-2	colon:	n/a
19	chr15:41806867-41806917	PANC-1	pancreas:	n/a
20	chr15:41832778-41832828	HEEpiC	esophagus:	n/a
21	chr15:41806867-41806917	NB4	blood:	n/a
22	chr15:41820721-41820771	PrEC	prostate:	n/a
23	chr15:41806867-41806917	BJ	skin:	n/a
24	chr15:41836038-41836088	AG09309	skin:	n/a
25	chr15:41836038-41836088	Hepatocyte	liver:	n/a
26	chr15:41806867-41806917	Hepatocyte	liver:	n/a
27	chr15:41820721-41820771	HIPEpiC	eye:	n/a
28	chr15:41836038-41836088	AG10803	skin:	n/a
29	chr15:41832778-41832828	PANC-1	pancreas:	n/a
30	chr15:41820721-41820771	GM19239	blood:	n/a
31	chr15:41820721-41820771	Jurkat	blood:	n/a
32	chr15:41806867-41806917	HUVEC	blood vessel:	n/a
33	chr15:41836038-41836088	CMK	blood:	n/a
34	chr15:41820721-41820771	BE2_C	brain:	n/a
35	chr15:41806867-41806917	HAEpiC	amniotic membrane:	n/a
36	chr15:41820721-41820771	U87	brain:	n/a
37	chr15:41832778-41832828	AoSMC	blood vessel:	n/a
38	chr15:41806867-41806917	AG09319	gingival:	n/a
39	chr15:41820721-41820771	CMK	blood:	n/a
40	chr15:41832778-41832828	AG04450	lung:	fetal
41	chr15:41820721-41820771	NHBE	bronchial:	n/a
42	chr15:41832778-41832828	SKMC	muscle:	n/a
43	chr15:41806867-41806917	LNCaP	prostate:	n/a
44	chr15:41832778-41832828	U87	brain:	n/a
45	chr15:41806867-41806917	ECC-1	luminal epithelium:	n/a
46	chr15:41832778-41832828	ProgFib	skin:	n/a
47	chr15:41806867-41806917	HNPCEpiC	eye:	n/a
48	chr15:41832778-41832828	GM19239	blood:	n/a
49	chr15:41820721-41820771	A549	lung:	n/a
50	chr15:41832778-41832828	GM12891	blood:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:41835700..41837704-chr15:42118864..42120391,2	K562	blood:
2	chr11:62609094..62609648-chr15:41836152..41836752,2	Hela-S3	cervix:
3	chr15:41823818..41827123-chr15:41828175..41831276,4	K562	blood:
4	chr15:41821217..41823173-chr15:41825451..41828342,2	K562	blood:
5	chr15:41814934..41817190-chr15:41828140..41829699,2	MCF-7	breast:
6	chr15:41784591..41787497-chr15:41813598..41816388,3	K562	blood:
7	chr15:41784244..41787186-chr15:41835793..41838130,2	MCF-7	breast:
8	chr15:41822152..41826086-chr15:41831755..41835975,4	K562	blood:
9	chr15:41811420..41814118-chr15:41817482..41820204,2	K562	blood:
10	chr15:41836090..41836866-chr19:17905832..17906456,2	Hela-S3	cervix:
11	chr15:41823818..41827123-chr15:41828175..41831276,4	K562	blood:
12	chr15:41813214..41815867-chr15:41821195..41823790,3	K562	blood:
13	chr15:41813214..41815755-chr15:41821195..41823682,2	K562	blood:
14	chr15:41827594..41830988-chr15:41833491..41835867,5	K562	blood:
15	chr15:41835948..41836538-chr8:17941062..17941618,2	NB4	blood:
16	chr15:41785172..41787151-chr15:41835585..41837884,2	MCF-7	breast:
17	chr15:41832281..41834359-chr15:41835096..41837787,3	K562	blood:
18	chr15:41812182..41819156-chr15:41830894..41838104,9	K562	blood:
19	chr15:41814934..41817190-chr15:41828140..41829699,2	MCF-7	breast:
20	chr15:41407191..41409421-chr15:41835564..41837898,2	MCF-7	breast:
21	chr15:41834571..41836708-chr15:41849262..41851156,2	K562	blood:
22	chr15:41766272..41768220-chr15:41833499..41835975,2	K562	blood:
23	chr15:41785345..41788204-chr15:41808714..41810718,3	K562	blood:
24	chr15:41807609..41810088-chr15:41818864..41820649,2	K562	blood:
25	chr15:41784287..41786620-chr15:41827580..41829440,3	K562	blood:
26	chr15:41805856..41809445-chr15:41809960..41813355,6	K562	blood:
27	chr15:41835713..41840265-chr15:41851401..41853463,4	K562	blood:
28	chr15:41812182..41819156-chr15:41830894..41838104,9	K562	blood:
29	chr15:41794324..41796894-chr15:41811831..41813969,3	K562	blood:
30	chr15:41812182..41814825-chr15:41833135..41836029,3	K562	blood:
31	chr15:41791755..41794361-chr15:41822033..41824334,2	K562	blood:
32	chr15:41785345..41788204-chr15:41809016..41810718,2	K562	blood:
33	chr15:41805856..41809445-chr15:41811162..41813355,3	K562	blood:
34	chr15:41811420..41814118-chr15:41817482..41820204,2	K562	blood:
35	chr15:41827251..41831779-chr15:41832424..41837409,12	K562	blood:
36	chr15:41819746..41824231-chr15:41825451..41829235,5	K562	blood:
37	chr15:41827251..41831779-chr15:41832424..41837409,12	K562	blood:
38	chr15:41783980..41786928-chr15:41835398..41839034,5	K562	blood:
39	chr15:41836113..41836929-chr9:140135486..140135990,2	HCT-116	colon:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RPAP1	hsa-miR-155-5p	chr15:41809400-41809422

Variant related genes	Relation type
LTK	TF binding region
RPAP1	TF binding region
LTK	CpG island
RPAP1	CpG island
ENSG00000128908	chromatin interactions
ENSG00000062524	chromatin interactions
ENSG00000250379	chromatin interactions
ENSG00000103932	chromatin interactions
ENSG00000137825	chromatin interactions
ENSG00000168970	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000243789	chromatin interactions
ENSG00000104763	chromatin interactions
ENSG00000137815	chromatin interactions
ENSG00000179913	chromatin interactions
ENSG00000092445	chromatin interactions
ENSG00000188229	chromatin interactions

Extended variants
information (count: 1357 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1357 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3759794	chr15:41806658-41806659	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs373840943	chr15:41806695-41806696	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs3759793	chr15:41806726-41806727	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs189398398	chr15:41806752-41806753	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs566707764	chr15:41806834-41806835	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs78288023	chr15:41806868-41806869	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs141100387	chr15:41806870-41806871	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs569178920	chr15:41806931-41806932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538106067	chr15:41806938-41806939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548384906	chr15:41806994-41806995	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs8035575	chr15:41807000-41807001	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs574350959	chr15:41807006-41807007	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs575648157	chr15:41807007-41807008	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs182135748	chr15:41807008-41807009	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs538836829	chr15:41807009-41807010	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs61306419	chr15:41807049-41807050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542972926	chr15:41807085-41807086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548005283	chr15:41807092-41807093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566208923	chr15:41807096-41807097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs8035331	chr15:41807127-41807128	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs28679582	chr15:41807135-41807136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs576704434	chr15:41807159-41807160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542506692	chr15:41807192-41807193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs117183246	chr15:41807200-41807201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185149283	chr15:41807206-41807207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547779662	chr15:41807217-41807218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs66616178	chr15:41807243-41807244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371871733	chr15:41807244-41807245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs113060711	chr15:41807248-41807249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541111631	chr15:41807255-41807256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564594703	chr15:41807275-41807276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114883056	chr15:41807289-41807290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146939917	chr15:41807304-41807305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs148057931	chr15:41807305-41807306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140907859	chr15:41807325-41807326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150128376	chr15:41807352-41807353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs71431817	chr15:41807365-41807366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs568228298	chr15:41807417-41807418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533802564	chr15:41807419-41807420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553303219	chr15:41807433-41807434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375169308	chr15:41807446-41807447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372190219	chr15:41807447-41807448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138595184	chr15:41807450-41807451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576558466	chr15:41807451-41807452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542194244	chr15:41807479-41807480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564643433	chr15:41807502-41807503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572624656	chr15:41807537-41807538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs142829751	chr15:41807612-41807613	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs564434962	chr15:41807613-41807614	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs533509775	chr15:41807614-41807615	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
Renal cell carcinoma	21215367	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1107 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41801800-41819000	Weak transcription	Hela-S3	cervix
2	chr15:41805200-41809200	Weak transcription	A549	lung
3	chr15:41806000-41806800	Flanking Active TSS	K562	blood
4	chr15:41806000-41809400	Weak transcription	Brain Angular Gyrus	brain
5	chr15:41806200-41806800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr15:41806200-41806800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
7	chr15:41806200-41806800	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr15:41806200-41806800	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr15:41806200-41806800	Enhancers	Stomach Mucosa	stomach
10	chr15:41806200-41808600	Weak transcription	Brain Cingulate Gyrus	brain
11	chr15:41806200-41809000	Weak transcription	Ovary	ovary
12	chr15:41806200-41809200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr15:41806200-41809200	Weak transcription	Left Ventricle	heart
14	chr15:41806200-41809600	Weak transcription	Colon Smooth Muscle	Colon
15	chr15:41806200-41809600	Weak transcription	Pancreas	Pancrea
16	chr15:41806200-41809600	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr15:41806200-41809600	Weak transcription	HMEC	breast
18	chr15:41806200-41815400	Weak transcription	NHDF-Ad	bronchial
19	chr15:41806200-41820400	Weak transcription	HSMM	muscle
20	chr15:41806200-41822600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr15:41806400-41806800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr15:41806400-41806800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr15:41806400-41806800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr15:41806400-41806800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr15:41806400-41806800	Strong transcription	Brain Substantia Nigra	brain
26	chr15:41806400-41807200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
27	chr15:41806400-41808200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr15:41806400-41808600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr15:41806400-41808600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr15:41806400-41808800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr15:41806400-41808800	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr15:41806400-41808800	Weak transcription	Fetal Intestine Small	intestine
33	chr15:41806400-41809000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr15:41806400-41809000	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr15:41806400-41809000	Weak transcription	Placenta	Placenta
36	chr15:41806400-41809000	Weak transcription	NHEK	skin
37	chr15:41806400-41809200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr15:41806400-41809200	Weak transcription	NHLF	lung
39	chr15:41806400-41809400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr15:41806400-41809400	Weak transcription	Adipose Nuclei	Adipose
41	chr15:41806400-41809400	Weak transcription	Brain Anterior Caudate	brain
42	chr15:41806400-41809400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr15:41806400-41809400	Weak transcription	Fetal Intestine Large	intestine
44	chr15:41806400-41809400	Weak transcription	Fetal Muscle Trunk	muscle
45	chr15:41806400-41809400	Weak transcription	Psoas Muscle	Psoas
46	chr15:41806400-41809400	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr15:41806400-41809400	Weak transcription	HSMMtube	muscle
48	chr15:41806400-41809600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr15:41806400-41809600	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr15:41806400-41809600	Weak transcription	Esophagus	oesophagus

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