Variant report

Variant	rs7561616
Chromosome Location	chr2:99907232-99907233
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:99905599..99909122-chr2:99945751..99948599,3	MCF-7	breast:
2	chr2:99906899..99908404-chr2:99910442..99912055,2	K562	blood:

Extended variants
information (count: 145 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:119)

rs_ID	r²[population]
rs1000409	0.82[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap]
rs1011633	0.84[JPT][hapmap]
rs10172068	0.91[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs10172752	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs10187843	0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs10207981	0.90[JPT][hapmap]
rs1053544	0.84[JPT][hapmap]
rs10779902	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11123775	0.87[CHB][hapmap];0.85[JPT][hapmap];0.88[ASN][1000 genomes]
rs11123777	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11123779	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11123782	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11123786	0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs11674219	0.80[ASN][1000 genomes]
rs11676581	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11683651	0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs11685870	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11686535	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11687328	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11687870	0.82[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.81[ASN][1000 genomes]
rs11884686	0.85[JPT][hapmap]
rs11892441	0.85[JPT][hapmap]
rs11892472	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11895206	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11897443	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11899745	0.84[JPT][hapmap]
rs11902994	0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs12464785	0.84[JPT][hapmap]
rs12615519	0.96[CEU][hapmap];0.82[EUR][1000 genomes]
rs12621141	0.84[ASN][1000 genomes]
rs12623540	0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs13004376	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13007100	0.85[EUR][1000 genomes]
rs13008948	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13009863	0.81[AMR][1000 genomes]
rs13009884	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13010416	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13011240	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13014360	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.88[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs13016182	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13017871	0.83[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs13018274	0.82[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs13019192	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13026997	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13033740	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1451243	0.82[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs1584647	0.85[JPT][hapmap]
rs1584648	0.85[JPT][hapmap]
rs17022433	0.86[CHB][hapmap];0.84[JPT][hapmap];0.88[ASN][1000 genomes]
rs17022629	0.85[JPT][hapmap]
rs1825770	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1955393	0.88[ASN][1000 genomes]
rs2242037	0.82[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap]
rs2290255	0.84[JPT][hapmap]
rs2290256	0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap]
rs2290257	0.85[JPT][hapmap]
rs2290261	0.84[JPT][hapmap]
rs2305354	0.82[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs2309585	0.91[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs2309617	0.85[JPT][hapmap]
rs3087386	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs3749087	0.85[JPT][hapmap]
rs3791212	0.85[JPT][hapmap]
rs3792134	0.91[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap]
rs3792137	0.89[JPT][hapmap]
rs3792142	0.84[JPT][hapmap]
rs3792146	0.90[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs3792149	0.91[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs3792152	0.95[CHB][hapmap];0.94[JPT][hapmap];0.85[YRI][hapmap]
rs3811555	0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.81[ASN][1000 genomes]
rs3828316	0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs4143760	0.85[JPT][hapmap]
rs4535093	0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs4850899	0.85[AFR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4850901	0.86[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.81[ASN][1000 genomes]
rs4851200	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4851205	0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs4851206	0.84[JPT][hapmap]
rs55867742	0.82[ASN][1000 genomes]
rs55991925	0.86[ASN][1000 genomes]
rs59816625	0.88[ASN][1000 genomes]
rs60294863	0.80[ASN][1000 genomes]
rs6542879	0.91[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs6542880	0.91[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs6542882	0.91[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs6708861	0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.81[ASN][1000 genomes]
rs6709240	0.81[ASN][1000 genomes]
rs6711977	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6714244	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs6721297	0.95[CHB][hapmap];0.84[YRI][hapmap]
rs6722617	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs6732397	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6734290	0.82[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.88[YRI][hapmap];0.82[ASN][1000 genomes]
rs6735381	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6753588	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs717454	0.84[JPT][hapmap]
rs7421284	0.87[ASN][1000 genomes]
rs7561079	0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs7563462	0.85[JPT][hapmap]
rs7567674	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs7570978	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7571202	0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.82[ASN][1000 genomes]
rs7574135	0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs7579403	0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs7580448	0.91[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs7585019	0.84[JPT][hapmap]
rs7585721	0.91[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs7587419	0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs7593274	0.85[JPT][hapmap]
rs7594838	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs7597141	0.85[JPT][hapmap]
rs7601470	0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs7601730	0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs7609108	0.82[ASN][1000 genomes]
rs769105	0.84[JPT][hapmap]
rs896248	0.82[JPT][hapmap]
rs896249	0.85[JPT][hapmap]
rs901596	0.88[ASN][1000 genomes]
rs959929	0.91[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431424	chr2:99652682-100494682	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv515702	chr2:99827733-99922967	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
3	nsv458685	chr2:99827733-99922967	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
4	nsv582519	chr2:99827733-99922967	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
5	nsv874698	chr2:99827733-99924918	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
6	nsv1001784	chr2:99838079-99910328	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
7	nsv535840	chr2:99838079-99910328	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
8	nsv458696	chr2:99838203-99922967	ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
9	nsv582520	chr2:99838203-99922967	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
10	nsv997436	chr2:99840131-99916886	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
11	nsv1009872	chr2:99840131-99924543	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
12	nsv1001194	chr2:99840131-99928323	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
13	esv2762746	chr2:99840143-99916898	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
14	nsv1005118	chr2:99841951-99924543	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
15	nsv1001736	chr2:99846306-99916886	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
16	nsv1009459	chr2:99846306-99918895	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
17	nsv1002169	chr2:99846306-99924543	Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
18	esv2751904	chr2:99847882-99913998	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
19	nsv1001235	chr2:99847890-99913998	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
20	nsv582521	chr2:99847890-99922967	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
21	nsv1007566	chr2:99847890-99924543	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
22	nsv999059	chr2:99847890-99926934	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
23	nsv1007249	chr2:99855978-99916886	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
24	nsv1004291	chr2:99855978-99919999	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
25	nsv1003262	chr2:99858556-99924543	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
26	nsv874699	chr2:99898998-100010044	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs7561616	REV1	Cis_1M	lymphoblastoid	RTeQTL
rs7561616	LIPT1	Cis_1M	lymphoblastoid	RTeQTL
rs7561616	REV1	cis	Thyroid	GTEx

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99879000-99933600	Weak transcription	Brain Cingulate Gyrus	brain
2	chr2:99880400-99907400	Weak transcription	Right Ventricle	heart
3	chr2:99892400-99918600	Weak transcription	Brain Anterior Caudate	brain
4	chr2:99892400-99935000	Weak transcription	Brain Angular Gyrus	brain
5	chr2:99894200-99934800	Weak transcription	Gastric	stomach
6	chr2:99895400-99935000	Weak transcription	Pancreas	Pancrea
7	chr2:99895800-99914400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr2:99895800-99921000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr2:99895800-99933600	Weak transcription	HSMM	muscle
10	chr2:99895800-99933600	Weak transcription	HSMMtube	muscle
11	chr2:99896800-99933400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr2:99897000-99918400	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr2:99897000-99933600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr2:99897200-99914600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr2:99897200-99918400	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr2:99897200-99933800	Weak transcription	Fetal Intestine Small	intestine
17	chr2:99897400-99933800	Weak transcription	HepG2	liver
18	chr2:99897600-99918800	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr2:99897800-99907400	Weak transcription	Adipose Nuclei	Adipose
20	chr2:99898200-99918800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr2:99898200-99934000	Weak transcription	Small Intestine	intestine
22	chr2:99898400-99938600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr2:99898600-99933800	Weak transcription	Colon Smooth Muscle	Colon
24	chr2:99899200-99918400	Weak transcription	Spleen	Spleen
25	chr2:99899400-99918600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr2:99899400-99933800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr2:99899600-99918600	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr2:99899600-99933000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr2:99899800-99935000	Weak transcription	Esophagus	oesophagus
30	chr2:99900000-99933600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr2:99900400-99933800	Weak transcription	Colonic Mucosa	Colon
32	chr2:99901000-99918600	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr2:99901200-99933400	Weak transcription	Primary B cells from cord blood	blood
34	chr2:99901200-99936600	Weak transcription	Fetal Brain Male	brain
35	chr2:99901400-99914400	Weak transcription	Thymus	Thymus
36	chr2:99901400-99918400	Weak transcription	Brain Germinal Matrix	brain
37	chr2:99901400-99918800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr2:99901400-99922800	Weak transcription	Ovary	ovary
39	chr2:99901600-99907600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr2:99901600-99907600	Weak transcription	Brain Substantia Nigra	brain
41	chr2:99901600-99907800	Weak transcription	Fetal Brain Female	brain
42	chr2:99901600-99918400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr2:99901600-99918600	Weak transcription	Primary T helper cells PMA-I stimulated	--
44	chr2:99901600-99918600	Weak transcription	Psoas Muscle	Psoas
45	chr2:99901600-99918600	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr2:99901600-99919800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr2:99901600-99933400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr2:99901600-99933600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr2:99901600-99933600	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr2:99901600-99933800	Weak transcription	Primary T cells fromperipheralblood	blood

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