Variant report

Variant	rs2108978
Chromosome Location	chr17:19861458-19861459
allele	A/G
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	GATA3	chr17:19861293-19861946	MCF-7	breast:	n/a	n/a
2	JUND	chr17:19861246-19862105	SK-N-SH	brain:	n/a	chr17:19861545-19861556
3	EP300	chr17:19861123-19861945	SK-N-SH	brain:	n/a	chr17:19861278-19861292
4	FOSL2	chr17:19861234-19861810	MCF-7	breast:	n/a	chr17:19861544-19861555
5	USF2	chr17:19861389-19861835	Hela-S3	cervix:	n/a	n/a
6	FOSL2	chr17:19861329-19861740	SK-N-SH	brain:	n/a	chr17:19861544-19861555
7	PBX3	chr17:19861169-19862077	SK-N-SH	brain:	n/a	chr17:19861933-19861942
8	SP1	chr17:19861179-19861988	A549	lung:	n/a	n/a
9	FOS	chr17:19861300-19861933	HUVEC	blood vessel:	n/a	chr17:19861545-19861556
10	GATA2	chr17:19861434-19861921	SH-SY5Y	brain:	n/a	n/a
11	SIN3AK20	chr17:19861302-19861879	A549	lung:	n/a	n/a
12	MYC	chr17:19861408-19861608	MCF10A-Er-Src	breast:	n/a	n/a
13	GATA3	chr17:19861381-19861909	MCF-7	breast:	n/a	n/a
14	GATA3	chr17:19861180-19862222	SK-N-SH	brain:	n/a	n/a
15	NR3C1	chr17:19861386-19861691	A549	lung:	n/a	n/a
16	JUN	chr17:19861358-19861751	K562	blood:	n/a	n/a
17	JUND	chr17:19861284-19861863	A549	lung:	n/a	chr17:19861545-19861556
18	HDAC2	chr17:19861335-19861844	MCF-7	breast:	n/a	n/a
19	TEAD4	chr17:19861109-19861826	A549	lung:	n/a	n/a
20	GATA3	chr17:19861052-19862148	A549	lung:	n/a	n/a
21	HDAC2	chr17:19861310-19861836	MCF-7	breast:	n/a	n/a
22	FOSL1	chr17:19861251-19861801	HCT-116	colon:	n/a	n/a
23	MAX	chr17:19861365-19861705	Hela-S3	cervix:	n/a	n/a
24	TEAD4	chr17:19861334-19861723	H1-hESC	embryonic stem cell:	n/a	n/a
25	MXI1	chr17:19861277-19861718	Hela-S3	cervix:	n/a	n/a
26	TCF12	chr17:19861169-19862015	SK-N-SH	brain:	n/a	n/a
27	NFIC	chr17:19861281-19861926	SK-N-SH	brain:	n/a	n/a
28	FOSL2	chr17:19861324-19861827	MCF-7	breast:	n/a	chr17:19861544-19861555
29	TEAD4	chr17:19861296-19861582	H1-hESC	embryonic stem cell:	n/a	n/a
30	MAFK	chr17:19861378-19861916	IMR90	lung:	n/a	n/a
31	EP300	chr17:19861308-19861677	SK-N-SH_RA	brain:	n/a	n/a
32	MYC	chr17:19861328-19861632	MCF10A-Er-Src	breast:	n/a	n/a
33	JUND	chr17:19861198-19861916	SK-N-SH	brain:	n/a	chr17:19861545-19861556
34	FOSL2	chr17:19861367-19861736	HepG2	liver:	n/a	chr17:19861544-19861555
35	SP1	chr17:19861241-19861898	A549	lung:	n/a	n/a
36	GATA3	chr17:19861340-19861897	A549	lung:	n/a	n/a
37	FOS	chr17:19861384-19861727	MCF10A-Er-Src	breast:	n/a	chr17:19861545-19861556
38	GATA3	chr17:19861323-19861830	T-47D	breast:	n/a	n/a
39	KAP1	chr17:19861294-19861875	U2OS	brain:	n/a	n/a
40	JUND	chr17:19861368-19861825	K562	blood:	n/a	chr17:19861545-19861556
41	CHD1	chr17:19861076-19862294	IMR90	lung:	n/a	n/a
42	JUN	chr17:19861298-19861789	Hela-S3	cervix:	n/a	n/a
43	GATA3	chr17:19861198-19862045	MCF-7	breast:	n/a	n/a
44	EP300	chr17:19861244-19861708	Hela-S3	cervix:	n/a	chr17:19861278-19861292
45	SIN3AK20	chr17:19861279-19861767	SK-N-SH	brain:	n/a	n/a
46	FOS	chr17:19861343-19861725	Hela-S3	cervix:	n/a	chr17:19861545-19861556
47	MAX	chr17:19861264-19861818	SK-N-SH	brain:	n/a	n/a
48	FOS	chr17:19861382-19861734	MCF10A-Er-Src	breast:	n/a	chr17:19861545-19861556
49	JUND	chr17:19861279-19861855	MCF-7	breast:	n/a	chr17:19861545-19861556
50	SIN3AK20	chr17:19861257-19861922	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:19861091..19865827-chr17:19879221..19882528,6	MCF-7	breast:

Variant related genes	Relation type
AKAP10	TF binding region
ENSG00000108599	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs11204419	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11204420	0.97[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11204421	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs119672	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[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];0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1479129	1.00[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];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1638525	1.00[CEU][hapmap];0.93[CHB][hapmap];0.81[YRI][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs166840	0.81[EUR][1000 genomes]
rs169412	1.00[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];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs169414	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs175921	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs175922	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1860302	0.94[CHB][hapmap];0.85[JPT][hapmap]
rs191865	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2013443	0.82[YRI][hapmap]
rs203450	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs203451	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs203452	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs203455	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs203456	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs203457	1.00[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];0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs203458	1.00[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];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs203459	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs203460	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs203461	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs203462	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs203465	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs203466	1.00[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];0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs203469	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs203470	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs203477	1.00[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];0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs203479	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs203481	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[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];0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs203482	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35003563	0.94[CHB][hapmap];0.86[CHD][hapmap];0.85[JPT][hapmap]
rs397969	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs427798	0.83[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs4479308	0.82[ASN][1000 genomes]
rs4924803	0.94[CHB][hapmap];0.86[CHD][hapmap];0.85[JPT][hapmap]
rs4925060	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4925065	0.94[CHB][hapmap];0.84[JPT][hapmap]
rs4925072	0.88[CHB][hapmap];0.86[CHD][hapmap];0.85[JPT][hapmap]
rs4925077	0.94[CHB][hapmap];0.86[CHD][hapmap];0.85[JPT][hapmap]
rs4925081	0.94[CHB][hapmap];0.86[CHD][hapmap];0.85[JPT][hapmap]
rs56153261	0.86[ASN][1000 genomes]
rs6587206	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7207625	0.87[CHB][hapmap];0.86[CHD][hapmap];0.85[JPT][hapmap]
rs7208025	0.94[CHB][hapmap];0.86[CHD][hapmap];0.85[JPT][hapmap]
rs7208365	0.94[CHB][hapmap];0.86[CHD][hapmap];0.85[JPT][hapmap]
rs7209734	0.94[CHB][hapmap];0.86[CHD][hapmap];0.85[JPT][hapmap]
rs7222403	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8066150	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs850623	1.00[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];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs860335	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs888423	0.94[CHB][hapmap];0.86[CHD][hapmap]
rs918227	0.87[CHB][hapmap];0.85[JPT][hapmap]
rs9899357	0.84[CEU][hapmap];0.80[GIH][hapmap];0.90[TSI][hapmap]
rs9907752	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9914273	1.00[CEU][hapmap];0.96[YRI][hapmap];0.84[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs9914304	0.85[EUR][1000 genomes]
rs9916675	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]

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	nsv1062853	chr17:19547912-20206601	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	nsv907868	chr17:19768924-20217122	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv907869	chr17:19795774-19926836	Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv833394	chr17:19827714-19999577	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv1060337	chr17:19828636-20204872	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv543257	chr17:19828636-20204872	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs2108978	AKAP10	cis	uninvolved skin	skin_eQTL
rs2108978	AKAP10	cis	multi-tissue	Pritchard
rs2108978	CYTSB	cis	cerebellum	SCAN
rs2108978	SNORD49B	cis	parietal	SCAN
rs2108978	AKAP10	cis	Lymphoblastoid	GTEx
rs2108978	AKAP10	cis	normal skin	skin_eQTL
rs2108978	AKAP10	cis	lesional skin	skin_eQTL
rs2108978	ALDH3A1	cis	parietal	SCAN
rs2108978	AKAP10	cis	lymphoblastoid	seeQTL
rs2108978	TMEM11	cis	cerebellum	SCAN

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:19840000-19879200	Weak transcription	Fetal Brain Male	brain
2	chr17:19846800-19875600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr17:19850600-19861600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr17:19850600-19879200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr17:19850600-19880200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr17:19850600-19880200	Weak transcription	Aorta	Aorta
7	chr17:19851600-19871600	Weak transcription	Colonic Mucosa	Colon
8	chr17:19852000-19871000	Weak transcription	Small Intestine	intestine
9	chr17:19852200-19862200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr17:19852200-19865000	Weak transcription	Ovary	ovary
11	chr17:19852200-19866000	Weak transcription	Spleen	Spleen
12	chr17:19852200-19879400	Weak transcription	Esophagus	oesophagus
13	chr17:19852200-19879600	Weak transcription	Right Ventricle	heart
14	chr17:19852200-19880000	Weak transcription	Psoas Muscle	Psoas
15	chr17:19852800-19869800	Weak transcription	Fetal Heart	heart
16	chr17:19854400-19864000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr17:19856600-19861800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
18	chr17:19857000-19868800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr17:19857200-19866400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr17:19857200-19867000	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr17:19857200-19875000	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr17:19857400-19873800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr17:19857400-19880400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr17:19857600-19866600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr17:19857600-19874000	Strong transcription	Dnd41	blood
26	chr17:19857600-19874400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr17:19857600-19875200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
28	chr17:19857600-19880200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr17:19857800-19866600	Strong transcription	Fetal Intestine Large	intestine
30	chr17:19858000-19866400	Strong transcription	Fetal Stomach	stomach
31	chr17:19858200-19867200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr17:19858400-19865600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr17:19858400-19873600	Strong transcription	Duodenum Mucosa	Duodenum
34	chr17:19858600-19865800	Strong transcription	Adipose Nuclei	Adipose
35	chr17:19858600-19874400	Strong transcription	Primary monocytes fromperipheralblood	blood
36	chr17:19858600-19875800	Strong transcription	Primary B cells from cord blood	blood
37	chr17:19858800-19861600	Strong transcription	HUES48 Cell Line	embryonic stem cell
38	chr17:19859000-19862000	Genic enhancers	Primary T cells from cord blood	blood
39	chr17:19859000-19877200	Strong transcription	Fetal Thymus	thymus
40	chr17:19859200-19861600	Strong transcription	H1 Cell Line	embryonic stem cell
41	chr17:19859200-19861600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
42	chr17:19859200-19862000	Strong transcription	Brain Germinal Matrix	brain
43	chr17:19859200-19866600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr17:19859200-19870800	Strong transcription	Primary T cells fromperipheralblood	blood
45	chr17:19859200-19874400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr17:19859200-19875600	Strong transcription	Placenta	Placenta
47	chr17:19859200-19878600	Strong transcription	Primary B cells from peripheral blood	blood
48	chr17:19859400-19861800	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
49	chr17:19859400-19862000	Strong transcription	Fetal Muscle Trunk	muscle
50	chr17:19859400-19862200	Strong transcription	Fetal Muscle Leg	muscle

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