Variant report

Variant	rs3788409
Chromosome Location	chr22:29198151-29198152
allele	G/T
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	MYC	chr22:29197674-29198581	K562	blood:	n/a	chr22:29198356-29198367 chr22:29198353-29198368 chr22:29198356-29198366 chr22:29198357-29198366 chr22:29198356-29198367 chr22:29198355-29198368
2	IKZF1	chr22:29198002-29198689	GM12878	blood:	n/a	chr22:29198515-29198523
3	RCOR1	chr22:29198107-29198432	HepG2	liver:	n/a	n/a
4	MYC	chr22:29197723-29198845	NB4	blood:	n/a	chr22:29198356-29198367 chr22:29198353-29198368 chr22:29198356-29198366 chr22:29198357-29198366 chr22:29198356-29198367 chr22:29198355-29198368
5	MYBL2	chr22:29197691-29198653	HepG2	liver:	n/a	n/a
6	POLR2A	chr22:29197764-29198222	MCF10A-Er-Src	breast:	n/a	n/a
7	MAX	chr22:29198005-29198656	MCF-7	breast:	n/a	chr22:29198356-29198367 chr22:29198353-29198368 chr22:29198356-29198366 chr22:29198357-29198366 chr22:29198356-29198367 chr22:29198355-29198368
8	SPI1	chr22:29198014-29198662	HL-60	blood:	n/a	chr22:29198426-29198435 chr22:29198425-29198438 chr22:29198424-29198437
9	ZNF384	chr22:29198105-29198921	K562	blood:	n/a	n/a
10	ARID3A	chr22:29197900-29199143	HepG2	liver:	n/a	n/a
11	PML	chr22:29197554-29198452	GM12878	blood:	n/a	n/a
12	POLR2A	chr22:29188106-29198866	HepG2	liver:	n/a	n/a
13	MYC	chr22:29198143-29198495	MCF10A-Er-Src	breast:	n/a	chr22:29198356-29198367 chr22:29198353-29198368 chr22:29198356-29198366 chr22:29198357-29198366 chr22:29198356-29198367 chr22:29198355-29198368
14	POLR2A	chr22:29197594-29199055	HL-60	blood:	n/a	n/a
15	RUNX3	chr22:29198150-29198538	GM12878	blood:	n/a	n/a
16	POLR2A	chr22:29194578-29198963	HepG2	liver:	n/a	n/a
17	POLR2A	chr22:29197413-29198559	HepG2	liver:	n/a	n/a
18	BHLHE40	chr22:29197871-29198544	GM12878	blood:	n/a	n/a
19	BCLAF1	chr22:29197977-29198361	GM12878	blood:	n/a	n/a
20	NFIC	chr22:29197546-29198503	GM12878	blood:	n/a	n/a
21	MYC	chr22:29197804-29198740	K562	blood:	n/a	chr22:29198356-29198367 chr22:29198353-29198368 chr22:29198356-29198366 chr22:29198357-29198366 chr22:29198356-29198367 chr22:29198355-29198368
22	POLR2A	chr22:29197557-29198903	HL-60	blood:	n/a	n/a
23	POLR2A	chr22:29197568-29198646	K562	blood:	n/a	n/a
24	POLR2A	chr22:29197885-29198492	MCF10A-Er-Src	breast:	n/a	n/a
25	SP1	chr22:29198066-29198584	HepG2	liver:	n/a	n/a
26	POLR2A	chr22:29198111-29198567	HepG2	liver:	n/a	n/a
27	POLR2A	chr22:29197602-29198190	GM12878	blood:	n/a	n/a
28	POLR2A	chr22:29198017-29198709	PBDE	blood:	n/a	n/a
29	POLR2A	chr22:29197537-29198506	GM12878	blood:	n/a	n/a
30	BHLHE40	chr22:29197983-29198864	HepG2	liver:	n/a	n/a
31	TAL1	chr22:29197843-29198626	K562	blood:	n/a	chr22:29198093-29198101
32	POLR2A	chr22:29198068-29198568	K562	blood:	n/a	n/a
33	MBD4	chr22:29197666-29198607	HepG2	liver:	n/a	n/a
34	MYC	chr22:29197921-29198578	K562	blood:	n/a	chr22:29198356-29198367 chr22:29198353-29198368 chr22:29198356-29198366 chr22:29198357-29198366 chr22:29198356-29198367 chr22:29198355-29198368
35	POLR2A	chr22:29197569-29198682	HepG2	liver:	n/a	n/a
36	POLR2A	chr22:29193840-29198990	HepG2	liver:	n/a	n/a
37	POLR2A	chr22:29186949-29198998	MCF-7	breast:	n/a	n/a
38	ELF1	chr22:29198084-29198715	MCF-7	breast:	n/a	n/a
39	MYC	chr22:29197590-29198889	K562	blood:	n/a	chr22:29198356-29198367 chr22:29198353-29198368 chr22:29198356-29198366 chr22:29198357-29198366 chr22:29198356-29198367 chr22:29198355-29198368
40	IRF1	chr22:29198075-29198533	K562	blood:	n/a	chr22:29198078-29198088
41	POLR2A	chr22:29198118-29198459	PFSK-1	brain:	n/a	n/a
42	CEBPB	chr22:29197728-29198265	GM12878	blood:	n/a	n/a
43	NR2F2	chr22:29197587-29198151	MCF-7	breast:	n/a	n/a
44	CHD1	chr22:29197966-29198316	GM12878	blood:	n/a	n/a
45	NFIC	chr22:29197848-29198551	HepG2	liver:	n/a	n/a
46	HEY1	chr22:29197601-29198517	K562	blood:	n/a	n/a
47	MAX	chr22:29197620-29198991	NB4	blood:	n/a	chr22:29198356-29198367 chr22:29198353-29198368 chr22:29198356-29198366 chr22:29198357-29198366 chr22:29198356-29198367 chr22:29198355-29198368
48	TEAD4	chr22:29197864-29198646	K562	blood:	n/a	n/a
49	TBP	chr22:29197508-29198989	HepG2	liver:	n/a	n/a
50	EP300	chr22:29197981-29198626	K562	blood:	n/a	chr22:29198426-29198435 chr22:29198179-29198193

No.	Distal block	Cell Line	Cell type
1	chr22:29137710..29139572-chr22:29196791..29200014,3	K562	blood:
2	chr20:55204332..55207187-chr22:29196441..29199381,2	MCF-7	breast:
3	chr10:15209689..15212599-chr22:29196455..29198324,2	MCF-7	breast:
4	chr11:118016321..118019019-chr22:29196202..29198424,2	MCF-7	breast:
5	chr2:191743958..191746252-chr22:29197423..29199172,2	MCF-7	breast:
6	chr22:29168270..29171327-chr22:29194850..29198169,6	MCF-7	breast:
7	chr22:29127658..29141630-chr22:29187451..29201381,67	MCF-7	breast:
8	chr12:52641358..52643792-chr22:29196072..29198510,2	MCF-7	breast:
9	chr22:29195813..29198298-chr4:36284011..36285845,2	MCF-7	breast:
10	chr20:19736824..19739326-chr22:29195217..29198180,3	MCF-7	breast:
11	chr22:29198007..29200457-chr22:29257019..29258581,2	K562	blood:
12	chr22:29165808..29174203-chr22:29186827..29200037,34	MCF-7	breast:
13	chr22:29167233..29170944-chr22:29195431..29200472,7	K562	blood:
14	chr22:29134224..29141746-chr22:29191206..29200044,27	MCF-7	breast:
15	chr22:29197206..29198818-chr3:25822984..25824967,2	MCF-7	breast:
16	chr22:29196345..29198539-chr8:144681842..144684762,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC117-1	chr22:29196562-29200517	NONHSAT084656

Variant related genes	Relation type
XBP1	TF binding region
ENSG00000152465	Chromatin interaction
ENSG00000087510	Chromatin interaction
ENSG00000177098	Chromatin interaction
ENSG00000233895	Chromatin interaction
ENSG00000271912	Chromatin interaction
ENSG00000170442	Chromatin interaction
ENSG00000135480	Chromatin interaction
ENSG00000115419	Chromatin interaction
ENSG00000151093	Chromatin interaction
ENSG00000268628	Chromatin interaction
ENSG00000100209	Chromatin interaction
ENSG00000159873	Chromatin interaction
ENSG00000183765	Chromatin interaction
ENSG00000197057	Chromatin interaction
ENSG00000151092	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs12165962	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.85[MEX][hapmap];0.97[TSI][hapmap]
rs12628211	0.96[ASN][1000 genomes]
rs132531	0.89[JPT][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap]
rs132533	0.89[JPT][hapmap]
rs132534	0.85[TSI][hapmap]
rs132536	0.83[CEU][hapmap];0.89[JPT][hapmap]
rs132539	0.83[CEU][hapmap];0.85[TSI][hapmap]
rs132548	0.89[JPT][hapmap];0.86[MEX][hapmap]
rs2064261	0.89[JPT][hapmap];0.95[MEX][hapmap];0.81[TSI][hapmap]
rs2097461	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2213645	0.84[JPT][hapmap]
rs2239815	0.96[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];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2269577	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2347447	0.94[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];0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2881635	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35259224	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs469989	0.86[CEU][hapmap]
rs469990	0.83[CEU][hapmap];0.89[JPT][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap];0.81[YRI][hapmap]
rs469991	0.83[CEU][hapmap];0.89[JPT][hapmap];0.80[YRI][hapmap]
rs4822998	0.82[JPT][hapmap]
rs5752795	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5752798	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5752801	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs5752804	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs5752807	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs5752809	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs5752812	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs5752813	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs5762784	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.86[MEX][hapmap];1.00[MKK][hapmap];0.92[TSI][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs5762788	0.94[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];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs5762795	0.96[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];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5762803	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5762815	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5762824	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs5762825	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs5762853	0.85[ASN][1000 genomes]
rs5762854	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs5762863	0.85[ASN][1000 genomes]
rs5762864	0.85[ASN][1000 genomes]
rs5762874	0.89[JPT][hapmap]
rs5762881	0.89[JPT][hapmap]
rs5762882	0.89[JPT][hapmap]
rs5762936	0.84[JPT][hapmap]
rs5997408	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6005867	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6005869	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6005872	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6005881	0.91[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.97[TSI][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6005892	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6005915	0.87[CHB][hapmap];0.95[JPT][hapmap];0.86[MEX][hapmap];0.82[TSI][hapmap]
rs6005916	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6005927	0.82[ASN][1000 genomes]
rs6005929	0.84[ASN][1000 genomes]
rs6519766	0.89[JPT][hapmap];0.95[MEX][hapmap];0.81[TSI][hapmap]
rs7287124	0.96[ASN][1000 genomes]
rs7287806	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7287918	0.89[JPT][hapmap];0.95[MEX][hapmap];0.81[TSI][hapmap]
rs763073	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8137969	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9620841	0.89[JPT][hapmap];0.95[MEX][hapmap];0.81[TSI][hapmap]
rs9625566	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9625588	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9625619	0.89[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916473	chr22:28837041-29215603	Weak transcription Bivalent Enhancer Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
2	nsv1064079	chr22:29065528-29456059	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	nsv834169	chr22:29095446-29303929	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs3788409	XBP1	cis	cerebellum	SCAN
rs3788409	MN1	cis	cerebellum	SCAN
rs3788409	XBP1	Cis_1M	lymphoblastoid	RTeQTL
rs3788409	SEZ6L	cis	cerebellum	SCAN
rs3788409	BEND4	trans	parietal	SCAN
rs3788409	CCDC117	Cis_1M	lymphoblastoid	RTeQTL
rs3788409	GAL3ST1	cis	cerebellum	SCAN

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29193200-29198800	Active TSS	Thymus	Thymus
2	chr22:29193800-29198200	Active TSS	Pancreas	Pancrea
3	chr22:29194000-29198200	Active TSS	Colonic Mucosa	Colon
4	chr22:29194000-29198400	Active TSS	Aorta	Aorta
5	chr22:29194400-29198600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr22:29195000-29198800	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr22:29195600-29198200	Active TSS	Brain Angular Gyrus	brain
8	chr22:29196600-29198400	Flanking Active TSS	Primary B cells from cord blood	blood
9	chr22:29196800-29198200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
10	chr22:29196800-29198400	Active TSS	Right Atrium	heart
11	chr22:29196800-29198800	Flanking Active TSS	Primary hematopoietic stem cells	blood
12	chr22:29196800-29199000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
13	chr22:29197000-29198600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
14	chr22:29197000-29199200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr22:29197000-29205400	Weak transcription	Spleen	Spleen
16	chr22:29197200-29198200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr22:29197200-29198400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
18	chr22:29197200-29198400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr22:29197200-29198600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
20	chr22:29197200-29198600	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr22:29197200-29202600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr22:29197200-29204000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr22:29197200-29208200	Weak transcription	Esophagus	oesophagus
24	chr22:29197200-29209800	Weak transcription	Left Ventricle	heart
25	chr22:29197200-29214200	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr22:29197200-29231600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr22:29197400-29198200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr22:29197400-29198200	Weak transcription	HSMMtube	muscle
29	chr22:29197400-29198400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr22:29197400-29198400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr22:29197400-29198400	Enhancers	Fetal Lung	lung
32	chr22:29197400-29198400	Enhancers	Lung	lung
33	chr22:29197400-29198400	Enhancers	HMEC	breast
34	chr22:29197400-29198600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
35	chr22:29197400-29198600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
36	chr22:29197400-29198600	Enhancers	Muscle Satellite Cultured Cells	--
37	chr22:29197400-29198600	Enhancers	Brain Cingulate Gyrus	brain
38	chr22:29197400-29198600	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr22:29197400-29198800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr22:29197400-29198800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr22:29197400-29198800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr22:29197400-29198800	Enhancers	Fetal Muscle Leg	muscle
43	chr22:29197400-29198800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
44	chr22:29197400-29198800	Enhancers	HUVEC	blood vessel
45	chr22:29197400-29198800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr22:29197400-29199000	Enhancers	Primary B cells from peripheral blood	blood
47	chr22:29197400-29199000	Flanking Active TSS	Fetal Thymus	thymus
48	chr22:29197400-29199000	Enhancers	Small Intestine	intestine
49	chr22:29197400-29214400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr22:29197400-29220400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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