Variant report

Variant	rs3759114
Chromosome Location	chr12:123757144-123757145
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:0)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:21 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr12:123756555-123757187	PANC-1	pancreas:	n/a	n/a
2	CTCF	chr12:123755537-123757196	SK-N-SH	brain:	n/a	chr12:123755750-123755763 chr12:123756337-123756350
3	ZKSCAN1	chr12:123756645-123757194	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr12:123756273-123757175	HepG2	liver:	n/a	n/a
5	REST	chr12:123756388-123757200	H1-neurons	neurons:	n/a	n/a
6	CHD1	chr12:123756638-123757278	H1-hESC	embryonic stem cell:	n/a	n/a
7	MXI1	chr12:123751836-123757238	SK-N-SH	brain:	n/a	chr12:123755352-123755361
8	MYBL2	chr12:123756507-123757148	HepG2	liver:	n/a	n/a
9	POLR2A	chr12:123756194-123757178	PANC-1	pancreas:	n/a	n/a
10	POLR2A	chr12:123754822-123757189	K562	blood:	n/a	n/a
11	MAZ	chr12:123753736-123757280	IMR90	lung:	n/a	chr12:123756093-123756102 chr12:123754155-123754164 chr12:123755815-123755825 chr12:123755367-123755376 chr12:123754240-123754250
12	POLR2A	chr12:123756069-123757201	HUVEC	blood vessel:	n/a	n/a
13	FOSL2	chr12:123756764-123757277	A549	lung:	n/a	n/a
14	REST	chr12:123756474-123757252	A549	lung:	n/a	n/a
15	POLR2A	chr12:123752762-123757235	H1-hESC	embryonic stem cell:	n/a	n/a
16	MTA3	chr12:123756552-123757232	GM12878	blood:	n/a	n/a
17	SP1	chr12:123756389-123757150	A549	lung:	n/a	chr12:123757094-123757106 chr12:123757095-123757105 chr12:123756678-123756692 chr12:123757095-123757109 chr12:123757096-123757105 chr12:123756683-123756692 chr12:123756917-123756926 chr12:123757094-123757106
18	POLR2A	chr12:123756220-123757198	SK-N-SH	brain:	n/a	n/a
19	TCF12	chr12:123756563-123757298	A549	lung:	n/a	n/a
20	POLR2A	chr12:123752165-123757291	H1-hESC	embryonic stem cell:	n/a	n/a
21	SIN3A	chr12:123756506-123757172	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:123755184..123757288-chr12:123772860..123774485,3	K562	blood:
2	chr12:123715831..123718104-chr12:123754466..123757204,4	MCF-7	breast:
3	chr12:123755747..123757789-chr12:123941373..123943090,2	K562	blood:
4	chr12:123717014..123719935-chr12:123753310..123757333,7	K562	blood:
5	chr1:115299292..115301809-chr12:123754705..123757686,2	MCF-7	breast:
6	chr12:123755058..123757440-chr12:124084744..124087456,3	K562	blood:
7	chr12:123753478..123757222-chr12:123871925..123875006,5	K562	blood:
8	chr12:123755222..123757665-chr12:123766639..123768783,2	MCF-7	breast:
9	chr12:123754759..123757395-chr12:123866766..123872450,7	MCF-7	breast:
10	chr12:123449665..123451282-chr12:123753748..123757462,3	MCF-7	breast:
11	chr12:123755164..123758333-chr12:123868507..123873426,5	K562	blood:
12	chr12:123753451..123758032-chr12:123846651..123850459,6	MCF-7	breast:
13	chr12:123756249..123757789-chr12:123941373..123944326,2	K562	blood:
14	chr12:123753293..123757508-chr12:124015727..124020202,5	K562	blood:
15	chr12:123755830..123757417-chr12:124116609..124118455,2	MCF-7	breast:
16	chr12:123756475..123758463-chr12:123849452..123851589,2	K562	blood:
17	chr12:123755285..123757528-chr12:124068793..124071301,3	MCF-7	breast:
18	chr12:123716353..123719935-chr12:123753594..123757800,6	K562	blood:
19	chr12:123718175..123719849-chr12:123755538..123757797,2	MCF-7	breast:
20	chr12:123737049..123739965-chr12:123755070..123757447,2	K562	blood:
21	chr12:123749757..123758492-chr12:123844437..123851411,15	MCF-7	breast:
22	chr12:123755389..123758333-chr12:123866833..123870129,4	K562	blood:

No data

Variant related genes	Relation type
CDK2AP1	TF binding region
ENSG00000270113	Chromatin interaction
ENSG00000111358	Chromatin interaction
ENSG00000130921	Chromatin interaction
ENSG00000199845	Chromatin interaction
ENSG00000139697	Chromatin interaction
ENSG00000184209	Chromatin interaction
ENSG00000150967	Chromatin interaction
ENSG00000247373	Chromatin interaction
ENSG00000188026	Chromatin interaction
ENSG00000256092	Chromatin interaction
ENSG00000111364	Chromatin interaction
ENSG00000111361	Chromatin interaction
ENSG00000009307	Chromatin interaction
ENSG00000051825	Chromatin interaction
ENSG00000086598	Chromatin interaction
ENSG00000183955	Chromatin interaction

Extended variants
information (count: 96 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs10444439	0.82[JPT][hapmap]
rs10732573	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs10734901	0.97[ASN][1000 genomes]
rs10744150	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs10744151	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10744152	1.00[CEU][hapmap];0.94[JPT][hapmap]
rs10772997	0.95[CHB][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs10772999	0.87[ASN][1000 genomes]
rs10773000	0.85[CHD][hapmap];0.84[JPT][hapmap]
rs10773002	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10846489	0.94[CHD][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs10846516	1.00[YRI][hapmap]
rs10846517	1.00[ASW][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];0.86[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap]
rs10846519	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap]
rs10846520	1.00[CEU][hapmap];0.88[JPT][hapmap]
rs10846523	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap]
rs11057202	0.83[ASN][1000 genomes]
rs11057205	0.87[ASN][1000 genomes]
rs11057207	0.87[ASN][1000 genomes]
rs11057209	0.88[ASN][1000 genomes]
rs11057219	0.80[ASN][1000 genomes]
rs11057223	0.83[CHB][hapmap];0.94[CHD][hapmap];0.84[JPT][hapmap]
rs11057224	0.82[ASN][1000 genomes]
rs11057239	1.00[YRI][hapmap]
rs11057265	1.00[YRI][hapmap]
rs11057278	1.00[YRI][hapmap]
rs11057287	1.00[CEU][hapmap];0.94[JPT][hapmap]
rs1109559	0.94[CHD][hapmap];0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs1109560	0.83[JPT][hapmap];0.83[ASN][1000 genomes]
rs11554169	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1568427	0.95[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs1568428	0.88[CHD][hapmap];0.84[JPT][hapmap]
rs1609520	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs1660	0.88[JPT][hapmap]
rs1727331	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs1879379	0.82[CHD][hapmap];0.84[JPT][hapmap]
rs1969355	0.96[ASN][1000 genomes]
rs1980251	0.97[ASN][1000 genomes]
rs2030401	0.81[ASN][1000 genomes]
rs2090764	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2271976	0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs2280424	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[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];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28362669	0.84[AFR][1000 genomes]
rs28414347	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap]
rs28501453	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap]
rs28587386	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap]
rs28595660	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs28613486	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap]
rs28698461	1.00[YRI][hapmap]
rs36121382	0.89[AFR][1000 genomes]
rs3759111	1.00[ASW][hapmap];0.91[CHB][hapmap];0.89[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes]
rs3759113	0.91[CHB][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap]
rs3803001	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap]
rs3825141	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap]
rs4148864	1.00[ASW][hapmap];1.00[YRI][hapmap]
rs4148865	1.00[YRI][hapmap]
rs4460848	0.91[CHB][hapmap];0.89[JPT][hapmap]
rs4474478	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4474479	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4553407	0.82[ASN][1000 genomes]
rs4594040	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4759367	0.90[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes]
rs4759372	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4759406	0.89[AFR][1000 genomes]
rs4759407	1.00[ASW][hapmap];0.91[CHB][hapmap];0.89[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes]
rs4759408	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs4759411	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4759413	1.00[CEU][hapmap];0.91[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4759414	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4759418	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57676984	0.89[AFR][1000 genomes]
rs60077920	0.89[AFR][1000 genomes]
rs60254089	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs60296110	0.89[AFR][1000 genomes]
rs61187102	0.83[AFR][1000 genomes]
rs61231969	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61519741	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61953394	0.82[ASN][1000 genomes]
rs6488869	1.00[CEU][hapmap]
rs6488870	1.00[CEU][hapmap]
rs7137286	0.87[ASN][1000 genomes]
rs7139321	0.84[JPT][hapmap]
rs7297649	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap]
rs7304782	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7486723	0.85[EUR][1000 genomes]
rs7959415	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap]
rs9284166	1.00[CEU][hapmap]
rs9795593	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1825473	chr12:123582855-123822503	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	esv1803368	chr12:123640853-123822503	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
3	esv1830566	chr12:123640853-123822503	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
4	esv1836043	chr12:123709409-123822503	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
5	esv3371786	chr12:123753799-123757997	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	20 gene(s)	inside rSNPs	diseases
6	esv3506414	chr12:123754849-123757572	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	20 gene(s)	inside rSNPs	diseases
7	esv3506415	chr12:123754849-123757572	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	20 gene(s)	inside rSNPs	diseases
8	esv3441214	chr12:123755024-123757572	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123753600-123757200	Active TSS	H9 Cell Line	embryonic stem cell
2	chr12:123754000-123757200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:123754000-123757200	Active TSS	Ovary	ovary
4	chr12:123754000-123757400	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr12:123754000-123757600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr12:123754200-123757200	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr12:123754200-123757200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr12:123754200-123757200	Active TSS	Aorta	Aorta
9	chr12:123754200-123757200	Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr12:123754200-123757200	Active TSS	HSMM	muscle
11	chr12:123754200-123757400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr12:123754200-123757400	Active TSS	HUES6 Cell Line	embryonic stem cell
13	chr12:123754800-123757200	Active TSS	Lung	lung
14	chr12:123755000-123757200	Active TSS	Breast Myoepithelial Primary Cells	Breast
15	chr12:123755000-123757200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:123755000-123757200	Active TSS	Brain Inferior Temporal Lobe	brain
17	chr12:123755000-123757200	Active TSS	Fetal Brain Female	brain
18	chr12:123755000-123757200	Active TSS	Psoas Muscle	Psoas
19	chr12:123755200-123757200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr12:123755200-123757200	Active TSS	Left Ventricle	heart
21	chr12:123755200-123757200	Active TSS	Right Ventricle	heart
22	chr12:123755200-123757200	Active TSS	K562	blood
23	chr12:123755400-123757200	Active TSS	Fetal Muscle Trunk	muscle
24	chr12:123755400-123757200	Active TSS	Skeletal Muscle Female	skeletal muscle
25	chr12:123755600-123757200	Active TSS	Skeletal Muscle Male	skeletal muscle
26	chr12:123756000-123757200	Active TSS	Right Atrium	heart
27	chr12:123756600-123757200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr12:123756600-123757200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr12:123756600-123757200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
30	chr12:123756600-123757200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
31	chr12:123756600-123757200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
32	chr12:123756600-123757200	Flanking Active TSS	Fetal Thymus	thymus
33	chr12:123756600-123757200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
34	chr12:123756600-123757200	Flanking Active TSS	Dnd41	blood
35	chr12:123756600-123757200	Flanking Active TSS	HMEC	breast
36	chr12:123756600-123757400	Active TSS	Fetal Kidney	kidney
37	chr12:123756600-123757600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr12:123756800-123757200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
39	chr12:123756800-123757200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr12:123756800-123757200	Enhancers	Primary B cells from peripheral blood	blood
41	chr12:123756800-123757200	Flanking Active TSS	Primary hematopoietic stem cells	blood
42	chr12:123756800-123757200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
43	chr12:123756800-123757200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
44	chr12:123756800-123757200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr12:123756800-123757200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
46	chr12:123756800-123757200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr12:123756800-123757200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr12:123756800-123757200	Flanking Active TSS	Brain Anterior Caudate	brain
49	chr12:123756800-123757200	Flanking Active TSS	Brain Cingulate Gyrus	brain
50	chr12:123756800-123757200	Flanking Active TSS	Brain Hippocampus Middle	brain

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