Variant report

Variant	rs1365610
Chromosome Location	chr15:45694610-45694611
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:473)
CpG islands
(count:122)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:473 , 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	POLR2A	chr15:45693792-45695227	GM12878	blood:	n/a	n/a
2	SIX5	chr15:45694335-45694717	A549	lung:	n/a	n/a
3	TAF1	chr15:45694226-45694749	GM12892	blood:	n/a	n/a
4	CEBPB	chr15:45694050-45695135	IMR90	lung:	n/a	n/a
5	POLR2A	chr15:45693983-45695356	Hela-S3	cervix:	n/a	n/a
6	POLR2A	chr15:45694204-45695771	GM12878	blood:	n/a	n/a
7	TBP	chr15:45694207-45694978	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr15:45694025-45694878	PFSK-1	brain:	n/a	n/a
9	HDAC2	chr15:45694306-45694780	MCF-7	breast:	n/a	chr15:45694523-45694532
10	GABPA	chr15:45694316-45695154	GM12878	blood:	n/a	chr15:45694521-45694535 chr15:45694523-45694532 chr15:45694562-45694569 chr15:45694521-45694530 chr15:45694521-45694532
11	YY1	chr15:45694328-45695871	HepG2	liver:	n/a	n/a
12	MAX	chr15:45693878-45695301	ECC-1	luminal epithelium:	n/a	n/a
13	NRF1	chr15:45694327-45694697	HepG2	liver:	n/a	chr15:45694521-45694535 chr15:45694523-45694532 chr15:45694562-45694569 chr15:45694521-45694530 chr15:45694521-45694532 chr15:45694521-45694532
14	GTF2F1	chr15:45694214-45694820	K562	blood:	n/a	n/a
15	TAF1	chr15:45694183-45695250	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr15:45694009-45695355	GM18526	blood:	n/a	n/a
17	GABPA	chr15:45694354-45694969	H1-hESC	embryonic stem cell:	n/a	chr15:45694521-45694535 chr15:45694523-45694532 chr15:45694562-45694569 chr15:45694521-45694530 chr15:45694521-45694532
18	E2F6	chr15:45694456-45694654	K562	blood:	n/a	chr15:45694522-45694531
19	POLR2A	chr15:45693992-45694956	HUVEC	blood vessel:	n/a	n/a
20	BRCA1	chr15:45694159-45694701	HepG2	liver:	n/a	n/a
21	POLR2A	chr15:45694272-45695176	A549	lung:	n/a	n/a
22	FOXP2	chr15:45694306-45694624	SK-N-MC	brain:	n/a	n/a
23	RAD21	chr15:45694337-45694732	H1-hESC	embryonic stem cell:	n/a	n/a
24	MAZ	chr15:45693871-45695868	K562	blood:	n/a	n/a
25	GABPA	chr15:45694218-45694787	K562	blood:	n/a	chr15:45694521-45694535 chr15:45694523-45694532 chr15:45694562-45694569 chr15:45694521-45694530 chr15:45694521-45694532
26	GTF2B	chr15:45694244-45694679	K562	blood:	n/a	n/a
27	TEAD4	chr15:45693921-45694804	K562	blood:	n/a	n/a
28	REST	chr15:45694292-45694764	PANC-1	pancreas:	n/a	n/a
29	CEBPD	chr15:45694222-45694722	HepG2	liver:	n/a	n/a
30	POLR2A	chr15:45693764-45695111	K562	blood:	n/a	n/a
31	POLR2A	chr15:45694215-45695179	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr15:45694160-45695038	MCF-7	breast:	n/a	n/a
33	GTF2F1	chr15:45693910-45694725	Hela-S3	cervix:	n/a	n/a
34	SPI1	chr15:45694433-45694651	GM12878	blood:	n/a	chr15:45694559-45694572
35	POLR2A	chr15:45694069-45694880	HCT-116	colon:	n/a	n/a
36	POLR2A	chr15:45694147-45695015	HCT-116	colon:	n/a	n/a
37	POLR2A	chr15:45693891-45695837	HepG2	liver:	n/a	n/a
38	HMGN3	chr15:45694371-45696019	K562	blood:	n/a	n/a
39	MAX	chr15:45694427-45695347	H1-hESC	embryonic stem cell:	n/a	n/a
40	NFYA	chr15:45694023-45694757	Hela-S3	cervix:	n/a	chr15:45694463-45694481
41	MAX	chr15:45693960-45696081	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr15:45694175-45694812	HepG2	liver:	n/a	n/a
43	PBX3	chr15:45694194-45694772	A549	lung:	n/a	n/a
44	BCL3	chr15:45694218-45694679	A549	lung:	n/a	n/a
45	MTA3	chr15:45693666-45695134	GM12878	blood:	n/a	n/a
46	SP1	chr15:45694187-45694711	HepG2	liver:	n/a	n/a
47	BHLHE40	chr15:45694311-45694710	GM12878	blood:	n/a	n/a
48	SP4	chr15:45694361-45694751	H1-hESC	embryonic stem cell:	n/a	n/a
49	E2F6	chr15:45694297-45695251	H1-hESC	embryonic stem cell:	n/a	chr15:45694522-45694531
50	TRIM28	chr15:45694063-45694776	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:45694565-45694615	GM12891	blood:	n/a
2	chr15:45694565-45694615	HEK293	kidney:	embryo
3	chr15:45694579-45694629	HCT-116	colon:	n/a
4	chr15:45694579-45694629	Jurkat	blood:	n/a
5	chr15:45694565-45694615	NB4	blood:	n/a
6	chr15:45694565-45694615	HCF	heart:	n/a
7	chr15:45694565-45694615	BE2_C	brain:	n/a
8	chr15:45694565-45694615	ProgFib	skin:	n/a
9	chr15:45694565-45694615	AG10803	skin:	n/a
10	chr15:45694579-45694629	HCF	heart:	n/a
11	chr15:45694579-45694629	SK-N-SH_RA	brain:	n/a
12	chr15:45694579-45694629	AoSMC	blood vessel:	n/a
13	chr15:45694565-45694615	SK-N-SH	brain:	n/a
14	chr15:45694565-45694615	NHBE	bronchial:	n/a
15	chr15:45694579-45694629	SAEC	small airway:	n/a
16	chr15:45694579-45694629	SK-N-MC	brain:	n/a
17	chr15:45694579-45694629	U87	brain:	n/a
18	chr15:45694579-45694629	A549	lung:	n/a
19	chr15:45694579-45694629	NHDF-neo	bronchial:	n/a
20	chr15:45694565-45694615	GM06990	blood:	n/a
21	chr15:45694579-45694629	GM12878	blood:	n/a
22	chr15:45694565-45694615	GM12892	blood:	n/a
23	chr15:45694579-45694629	GM06990	blood:	n/a
24	chr15:45694565-45694615	HAEpiC	amniotic membrane:	n/a
25	chr15:45694579-45694629	HEK293	kidney:	embryo
26	chr15:45694579-45694629	CMK	blood:	n/a
27	chr15:45694565-45694615	K562	blood:	n/a
28	chr15:45694579-45694629	IMR90	lung:	fetal
29	chr15:45694565-45694615	RPTEC	kidney:	n/a
30	chr15:45694565-45694615	HRCEpiC	kidney:	n/a
31	chr15:45694565-45694615	AG04449	skin:	fetal
32	chr15:45694579-45694629	AG09319	gingival:	n/a
33	chr15:45694579-45694629	GM12891	blood:	n/a
34	chr15:45694579-45694629	HepG2	liver:	n/a
35	chr15:45694579-45694629	PrEC	prostate:	n/a
36	chr15:45694579-45694629	HL-60	blood:	n/a
37	chr15:45694579-45694629	Hepatocyte	liver:	n/a
38	chr15:45694579-45694629	LNCaP	prostate:	n/a
39	chr15:45694579-45694629	GM12892	blood:	n/a
40	chr15:45694579-45694629	K562	blood:	n/a
41	chr15:45694565-45694615	PANC-1	pancreas:	n/a
42	chr15:45694565-45694615	GM19239	blood:	n/a
43	chr15:45694579-45694629	HNPCEpiC	eye:	n/a
44	chr15:45694565-45694615	H1-hESC	embryonic stem cell:	embryo
45	chr15:45694579-45694629	HRCEpiC	kidney:	n/a
46	chr15:45694579-45694629	ovcar-3	ovarian:	n/a
47	chr15:45694565-45694615	Hela-S3	cervix:	n/a
48	chr15:45694579-45694629	NB4	blood:	n/a
49	chr15:45694565-45694615	HRPEpiC	eye:	n/a
50	chr15:45694565-45694615	T-47D	breast:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:45471561..45475350-chr15:45693833..45697444,3	MCF-7	breast:
2	chr12:44199711..44200638-chr15:45694089..45695040,2	NB4	blood:
3	chr15:45443245..45445612-chr15:45693741..45696247,2	K562	blood:
4	chr15:45491292..45493253-chr15:45693461..45696308,4	K562	blood:
5	chr15:45694437..45696115-chr8:101962201..101965108,2	MCF-7	breast:
6	chr15:45459071..45462844-chr15:45693635..45696532,4	K562	blood:
7	chr15:45693902..45696245-chr15:45709725..45712520,2	K562	blood:
8	chr15:45570708..45573284-chr15:45693152..45695793,2	MCF-7	breast:
9	chr15:45693976..45694707-chrX:48957687..48958360,2	HCT-116	colon:
10	chr15:45694071..45694958-chr7:104653061..104653666,2	Hela-S3	cervix:
11	chr15:45458882..45460694-chr15:45692968..45695992,3	MCF-7	breast:
12	chr15:45694132..45694822-chr5:68665207..68665996,2	HCT-116	colon:
13	chr15:45693513..45696404-chr15:45876472..45881031,4	MCF-7	breast:
14	chr15:45489573..45492565-chr15:45693942..45696435,3	MCF-7	breast:
15	chr15:44955315..44955922-chr15:45694323..45695000,2	NB4	blood:
16	chr15:45693986..45696362-chr15:45736299..45740535,4	MCF-7	breast:
17	chr15:45497455..45498005-chr15:45694577..45695511,2	K562	blood:
18	chr15:45490733..45493253-chr15:45692978..45696308,3	K562	blood:
19	chr15:45694563..45696942-chr15:45878361..45881039,2	K562	blood:
20	chr15:45693917..45694984-chr6:160210614..160211334,3	Hela-S3	cervix:
21	chr15:45459427..45462384-chr15:45693635..45696116,3	K562	blood:
22	chr15:45693029..45695760-chr15:45741637..45746369,4	MCF-7	breast:
23	chr15:45694529..45695513-chr17:27046875..27047495,2	Hela-S3	cervix:
24	chr15:45694225..45694845-chr7:100025841..100026828,2	Hela-S3	cervix:
25	chr15:45694198..45696265-chr15:45878361..45881505,3	K562	blood:
26	chr10:74033457..74033981-chr15:45693872..45694794,2	NB4	blood:
27	chr15:45693316..45695933-chr15:45878534..45881095,2	MCF-7	breast:
28	chr15:45493253..45495607-chr15:45694426..45696533,2	K562	blood:
29	chr1:28975072..28975687-chr15:45694096..45694823,2	HCT-116	colon:
30	chr15:45694376..45695055-chr3:128444885..128445547,3	Hela-S3	cervix:
31	chr15:45694469..45695046-chr5:43483496..43484152,3	Hela-S3	cervix:

No data

Variant related genes	Relation type
GATM	TF binding region
SPATA5L1	TF binding region
SPATA5L1	CpG island
GATM	CpG island
ENSG00000171763	Chromatin interaction
ENSG00000112110	Chromatin interaction
ENSG00000259519	Chromatin interaction
ENSG00000260035	Chromatin interaction
ENSG00000151239	Chromatin interaction
ENSG00000196998	Chromatin interaction
ENSG00000138606	Chromatin interaction
ENSG00000260170	Chromatin interaction
ENSG00000085231	Chromatin interaction
ENSG00000259520	Chromatin interaction
ENSG00000270103	Chromatin interaction
ENSG00000259539	Chromatin interaction
ENSG00000137857	Chromatin interaction
ENSG00000152942	Chromatin interaction
ENSG00000249492	Chromatin interaction
ENSG00000228393	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000198242	Chromatin interaction
ENSG00000146834	Chromatin interaction
ENSG00000164924	Chromatin interaction
ENSG00000168209	Chromatin interaction
ENSG00000120438	Chromatin interaction
ENSG00000075785	Chromatin interaction
ENSG00000259932	Chromatin interaction
ENSG00000259354	Chromatin interaction
ENSG00000151881	Chromatin interaction
ENSG00000104133	Chromatin interaction
ENSG00000104164	Chromatin interaction
ENSG00000252285	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 22 )

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10444821	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1049508	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap]
rs10519022	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap]
rs1145076	0.83[MEX][hapmap]
rs1145077	0.83[MEX][hapmap]
rs1145091	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap]
rs1153849	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap]
rs1153858	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap]
rs11632920	0.83[MEX][hapmap]
rs11639420	0.83[MEX][hapmap]
rs12437840	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap]
rs12437887	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap]
rs12440038	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];0.95[YRI][hapmap]
rs12593370	0.93[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap]
rs12593402	0.81[CEU][hapmap];0.84[JPT][hapmap]
rs1288775	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12908818	0.83[MEX][hapmap]
rs12909158	0.93[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap]
rs12913645	0.93[JPT][hapmap];0.92[MEX][hapmap]
rs1346266	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs1346267	0.83[MEX][hapmap]
rs1346268	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap]
rs1554521	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap]
rs16941017	0.86[JPT][hapmap]
rs16943246	1.00[CEU][hapmap]
rs1706824	0.93[JPT][hapmap];0.92[MEX][hapmap]
rs1719231	0.85[CEU][hapmap]
rs1719247	0.93[CEU][hapmap];0.92[CHB][hapmap];0.90[CHD][hapmap];0.93[JPT][hapmap];1.00[MEX][hapmap];0.84[TSI][hapmap]
rs1719250	0.87[MEX][hapmap]
rs1820518	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs1980288	0.93[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap];0.88[YRI][hapmap]
rs2056493	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap]
rs2066090	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2413768	0.83[MEX][hapmap]
rs2413769	0.93[JPT][hapmap];0.92[MEX][hapmap]
rs2413775	0.85[JPT][hapmap]
rs2433228	0.86[JPT][hapmap]
rs2433229	0.85[JPT][hapmap]
rs2461702	1.00[CEU][hapmap]
rs2461705	0.83[MEX][hapmap]
rs2467858	0.93[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs2668747	0.93[CEU][hapmap]
rs3759895	0.86[JPT][hapmap]
rs3759899	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap]
rs3809472	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs4395020	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap]
rs4627277	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4774550	0.86[JPT][hapmap]
rs4774580	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs4775911	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];0.88[TSI][hapmap];1.00[YRI][hapmap]
rs6493144	0.83[MEX][hapmap]
rs7164602	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap]
rs7167146	0.83[MEX][hapmap]
rs7171577	1.00[CEU][hapmap];0.81[YRI][hapmap]
rs8024620	0.83[MEX][hapmap]
rs8032904	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs872192	0.83[MEX][hapmap]
rs9806699	0.81[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916374	chr15:45058112-45769052	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv932147	chr15:45319178-45872076	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv869616	chr15:45401411-45736209	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	nsv569315	chr15:45446156-45772448	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
5	nsv469721	chr15:45608881-45788002	Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
6	nsv482380	chr15:45608881-45788002	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases

mRNA abundance (count:22)

SNP	Gene	Cis/trans	Tissue	Source
rs1365610	GATM	cis	cerebellum	SCAN
rs1365610	CTD-2651B20.4	cis	Artery Tibial	GTEx
rs1365610	SPTBN5	cis	parietal	SCAN
rs1365610	SHF	cis	parietal	SCAN
rs1365610	BMF	cis	parietal	SCAN
rs1365610	CTD-2651B20.4	cis	Nerve Tibial	GTEx
rs1365610	SP4	trans	parietal	SCAN
rs1365610	GATM	cis	Muscle Skeletal	GTEx
rs1365610	CTD-2651B20.3	cis	Nerve Tibial	GTEx
rs1365610	SPATA5L1	cis	lung	GTEx
rs1365610	SPATA5L1	cis	Thyroid	GTEx
rs1365610	SPATA5L1	cis	Nerve Tibial	GTEx
rs1365610	CTD-2651B20.3	cis	Esophagus Muscularis	GTEx
rs1365610	CTD-2651B20.3	cis	Artery Tibial	GTEx
rs1365610	CTD-2651B20.3	cis	Thyroid	GTEx
rs1365610	SPATA5L1	cis	cerebellum	SCAN
rs1365610	SPATA5L1	cis	Esophagus Muscularis	GTEx
rs1365610	CTD-2651B20.3	cis	lung	GTEx
rs1365610	CTD-2651B20.3	cis	Muscle Skeletal	GTEx
rs1365610	SPATA5L1	cis	Whole Blood	GTEx
rs1365610	CTD-2651B20.3	cis	Adipose Subcutaneous	GTEx
rs1365610	SPATA5L1	cis	parietal	SCAN

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45693200-45695000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr15:45693200-45696000	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr15:45693200-45696400	Active TSS	Aorta	Aorta
4	chr15:45693200-45696800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr15:45693400-45695600	Active TSS	Brain Anterior Caudate	brain
6	chr15:45693400-45696000	Active TSS	iPS-18 Cell Line	embryonic stem cell
7	chr15:45693400-45696000	Active TSS	Duodenum Smooth Muscle	Duodenum
8	chr15:45693400-45696200	Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr15:45693400-45696600	Active TSS	H1 Cell Line	embryonic stem cell
10	chr15:45693400-45697000	Active TSS	Fetal Intestine Large	intestine
11	chr15:45693400-45697600	Active TSS	GM12878-XiMat	blood
12	chr15:45693600-45694800	Active TSS	Breast Myoepithelial Primary Cells	Breast
13	chr15:45693600-45694800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr15:45693600-45694800	Active TSS	Colonic Mucosa	Colon
15	chr15:45693600-45695400	Active TSS	Right Ventricle	heart
16	chr15:45693600-45695600	Active TSS	Fetal Thymus	thymus
17	chr15:45693600-45695800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
18	chr15:45693600-45695800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr15:45693600-45695800	Active TSS	Fetal Brain Male	brain
20	chr15:45693600-45695800	Active TSS	K562	blood
21	chr15:45693600-45696000	Active TSS	HUES64 Cell Line	embryonic stem cell
22	chr15:45693600-45696000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr15:45693600-45696000	Active TSS	Muscle Satellite Cultured Cells	--
24	chr15:45693600-45696000	Active TSS	Fetal Intestine Small	intestine
25	chr15:45693600-45696000	Active TSS	Fetal Stomach	stomach
26	chr15:45693600-45696200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr15:45693600-45696200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr15:45693600-45696200	Active TSS	NHDF-Ad	bronchial
29	chr15:45693600-45696200	Active TSS	NHLF	lung
30	chr15:45693600-45696400	Active TSS	A549	lung
31	chr15:45693600-45696600	Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr15:45693600-45696600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr15:45693600-45696600	Active TSS	Psoas Muscle	Psoas
34	chr15:45693600-45697000	Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr15:45693600-45697200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr15:45693800-45694800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr15:45693800-45695000	Active TSS	Stomach Smooth Muscle	stomach
38	chr15:45693800-45695400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr15:45693800-45695600	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
40	chr15:45693800-45695600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr15:45693800-45695600	Active TSS	Placenta	Placenta
42	chr15:45693800-45695800	Active TSS	Brain Substantia Nigra	brain
43	chr15:45693800-45695800	Active TSS	Fetal Muscle Leg	muscle
44	chr15:45693800-45695800	Active TSS	Sigmoid Colon	Sigmoid Colon
45	chr15:45693800-45696000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr15:45693800-45696000	Active TSS	iPS-15b Cell Line	embryonic stem cell
47	chr15:45693800-45696000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr15:45693800-45696000	Active TSS	Colon Smooth Muscle	Colon
49	chr15:45693800-45696000	Active TSS	Esophagus	oesophagus
50	chr15:45693800-45696000	Active TSS	Gastric	stomach

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