Variant report

Variant	rs12713798
Chromosome Location	chr2:73986421-73986422
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:73985032..73987699-chr2:74002140..74003888,2	K562	blood:
2	chr2:73977687..73979772-chr2:73985866..73987487,2	K562	blood:
3	chr2:73981031..73983737-chr2:73985757..73987804,3	K562	blood:
4	chr2:73964182..73967073-chr2:73986238..73988087,2	K562	blood:
5	chr2:73985324..73987397-chr2:74002971..74004836,2	MCF-7	breast:
6	chr2:73985050..73987926-chr2:73998150..74000912,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C2orf78-3	chr2:73982148-73988270	NONHSAT071632

No data

Variant related genes	Relation type
ENSG00000273245	Chromatin interaction
ENSG00000144034	Chromatin interaction

Extended variants
information (count: 121 )
Associated
traits (count: 9 )

rSNPs within LD-proxies of this variant (count:114)

rs_ID	r²[population]
rs10172044	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10190002	0.81[TSI][hapmap]
rs10191988	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10193032	0.81[CHB][hapmap];0.81[CHD][hapmap];0.83[TSI][hapmap];0.84[ASN][1000 genomes]
rs10203740	0.88[CEU][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10208995	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1052161	0.81[TSI][hapmap]
rs11126414	0.87[CEU][hapmap];1.00[GIH][hapmap];0.87[MEX][hapmap];0.90[TSI][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11126415	0.91[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11126416	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11126417	1.00[CEU][hapmap];0.87[CHB][hapmap];0.90[GIH][hapmap];0.90[JPT][hapmap];1.00[TSI][hapmap];0.98[EUR][1000 genomes]
rs11891140	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11892172	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11894953	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12052539	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12053242	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12233112	0.87[CEU][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12233115	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12611487	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12612423	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12615807	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12618600	0.83[TSI][hapmap]
rs12619258	0.87[CEU][hapmap];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12624267	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.95[TSI][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12713788	0.84[EUR][1000 genomes]
rs12713789	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12713790	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12713791	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12713793	0.93[ASW][hapmap];1.00[CEU][hapmap];0.81[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12713794	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12713795	1.00[CEU][hapmap];0.96[YRI][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12713797	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12992607	1.00[CEU][hapmap];0.81[CHB][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12997568	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12998980	0.87[CEU][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13000788	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13003035	1.00[CEU][hapmap];0.81[CHB][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13005729	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13006448	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13006598	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13013228	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13014700	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13015885	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13017182	0.84[GIH][hapmap]
rs13020517	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13031853	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13031866	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13033744	0.91[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1320374	0.81[TSI][hapmap]
rs13383097	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17350056	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17350125	0.91[CEU][hapmap];0.88[YRI][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17350188	1.00[ASW][hapmap];1.00[CEU][hapmap];0.81[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.96[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17434634	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17434655	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1806683	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1815028	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2001436	0.92[CEU][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2001490	0.87[CEU][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2006997	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2012574	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2116367	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2272051	0.96[CEU][hapmap];0.81[CHB][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2272178	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2421557	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2421558	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2421559	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.96[MEX][hapmap];0.88[MKK][hapmap];0.95[TSI][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2421574	0.92[GIH][hapmap];0.83[MEX][hapmap];0.86[TSI][hapmap]
rs2421575	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2421586	0.83[TSI][hapmap]
rs2421668	0.83[TSI][hapmap]
rs2421672	0.96[CEU][hapmap];0.81[CHB][hapmap];0.88[YRI][hapmap];0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2421674	1.00[ASW][hapmap];1.00[CEU][hapmap];0.81[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.95[LWK][hapmap];0.96[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2421675	1.00[CEU][hapmap];0.81[CHB][hapmap];0.85[YRI][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2421676	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2421677	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2462127	0.88[CEU][hapmap];0.81[CHB][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35498419	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35767294	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35791379	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3813228	0.96[CEU][hapmap];0.81[CHB][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3980695	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4241257	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4358149	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4513320	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4530394	0.84[EUR][1000 genomes]
rs4852316	0.89[EUR][1000 genomes]
rs4852972	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4852975	0.87[CEU][hapmap];1.00[GIH][hapmap];0.88[MEX][hapmap];0.90[TSI][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4852976	0.91[CEU][hapmap];1.00[GIH][hapmap];0.92[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4852977	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4852978	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6732812	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6745560	0.82[GIH][hapmap];0.83[MEX][hapmap]
rs6748233	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6749841	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6750494	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6750515	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6750877	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6755500	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7210	1.00[ASW][hapmap];1.00[CEU][hapmap];0.81[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];0.96[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs732778	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7368570	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs7370393	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7558546	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7570683	0.83[TSI][hapmap]
rs7591112	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7597302	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7599453	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7606947	0.92[GIH][hapmap];0.91[MEX][hapmap];0.86[TSI][hapmap]
rs891695	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs891696	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9309475	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9309476	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428051	chr2:73717032-74030067	ZNF genes & repeats Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	esv2757806	chr2:73717032-74078592	Active TSS Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	esv2759060	chr2:73717032-74078592	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	nsv1013385	chr2:73822056-74041441	Strong transcription Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
5	nsv834260	chr2:73906106-74076520	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
6	nsv998315	chr2:73919185-74003998	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
7	nsv1000675	chr2:73919185-74038946	Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

mRNA abundance (count:9)

SNP	Gene	Cis/trans	Tissue	Source
rs12713798	ALMS1P	cis	parietal	SCAN
rs12713798	TPRKB	Cis_1M	lymphoblastoid	RTeQTL
rs12713798	CGI-121	cis	multi-tissue	Pritchard
rs12713798	DUSP11	cis	cerebellum	SCAN
rs12713798	DUSP11	cis	parietal	SCAN
rs12713798	ALMS1P	cis	Nerve Tibial	GTEx
rs12713798	ALMS1	cis	cerebellum	SCAN
rs12713798	ALMS1	Cis_1M	lymphoblastoid	RTeQTL
rs12713798	ALMS1	cis	parietal	SCAN

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73964600-74005400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:73965000-73993000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr2:73965400-73986600	Weak transcription	Psoas Muscle	Psoas
4	chr2:73966200-73992000	Weak transcription	Stomach Mucosa	stomach
5	chr2:73969400-73987200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr2:73971400-74002200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr2:73971600-73987000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr2:73972000-73992200	Weak transcription	Fetal Kidney	kidney
9	chr2:73973400-73987400	Weak transcription	Colonic Mucosa	Colon
10	chr2:73974000-73989000	Weak transcription	Fetal Brain Male	brain
11	chr2:73974200-73986800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr2:73974400-73987000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr2:73976600-74004400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr2:73977200-73995000	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr2:73977400-73993000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr2:73977400-74001400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr2:73977400-74004800	Strong transcription	Duodenum Mucosa	Duodenum
18	chr2:73977600-74004800	Strong transcription	Primary neutrophils fromperipheralblood	blood
19	chr2:73977800-74004000	Strong transcription	Primary B cells from peripheral blood	blood
20	chr2:73978000-74004200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr2:73978200-73998400	Strong transcription	Fetal Muscle Trunk	muscle
22	chr2:73978800-73995200	Strong transcription	Primary T helper cells PMA-I stimulated	--
23	chr2:73980000-73987200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr2:73980000-73988800	Weak transcription	K562	blood
25	chr2:73980200-73986600	Weak transcription	Brain Substantia Nigra	brain
26	chr2:73980600-73986800	Weak transcription	Brain Angular Gyrus	brain
27	chr2:73980800-73986600	Weak transcription	HSMMtube	muscle
28	chr2:73980800-73991400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr2:73981400-73994000	Strong transcription	Thymus	Thymus
30	chr2:73981600-74004800	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr2:73981800-73986600	Strong transcription	NH-A	brain
32	chr2:73981800-73986800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr2:73981800-73994000	Strong transcription	Fetal Stomach	stomach
34	chr2:73982000-74004600	Strong transcription	Primary T cells from cord blood	blood
35	chr2:73982000-74004800	Strong transcription	Primary monocytes fromperipheralblood	blood
36	chr2:73982000-74005200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:73982200-73986600	Strong transcription	HSMM	muscle
38	chr2:73982200-73988000	Strong transcription	NHEK	skin
39	chr2:73982200-73997200	Strong transcription	Primary B cells from cord blood	blood
40	chr2:73982200-73998400	Strong transcription	Fetal Intestine Large	intestine
41	chr2:73982200-74002600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr2:73982200-74004000	Strong transcription	Dnd41	blood
43	chr2:73982200-74004800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr2:73982200-74005200	Strong transcription	Primary T cells fromperipheralblood	blood
45	chr2:73982400-73986600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr2:73982400-73990400	Strong transcription	Sigmoid Colon	Sigmoid Colon
47	chr2:73982400-74002400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr2:73982400-74002600	Strong transcription	Muscle Satellite Cultured Cells	--
49	chr2:73982400-74004800	Strong transcription	Placenta	Placenta
50	chr2:73982400-74005000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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