Variant report

Variant	rs4530394
Chromosome Location	chr2:73929650-73929651
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:9 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RXRA	chr2:73929060-73930010	HepG2	liver:	n/a	n/a
2	FOSL2	chr2:73929536-73930191	HepG2	liver:	n/a	n/a
3	FOXA1	chr2:73929135-73929934	HepG2	liver:	n/a	n/a
4	FOXA1	chr2:73929062-73929918	HepG2	liver:	n/a	n/a
5	MYBL2	chr2:73928966-73930330	HepG2	liver:	n/a	n/a
6	MYBL2	chr2:73929072-73930016	HepG2	liver:	n/a	n/a
7	RXRA	chr2:73929632-73929903	HepG2	liver:	n/a	n/a
8	FOXA1	chr2:73929470-73929800	HepG2	liver:	n/a	n/a
9	SP1	chr2:73929021-73929987	HepG2	liver:	n/a	chr2:73929669-73929683

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:73929634-73929684	PFSK-1	brain:	n/a
2	chr2:73929634-73929684	HL-60	blood:	n/a
3	chr2:73929634-73929684	HCM	heart:	n/a
4	chr2:73929634-73929684	GM19239	blood:	n/a
5	chr2:73929634-73929684	NB4	blood:	n/a
6	chr2:73929634-73929684	NHBE	bronchial:	n/a
7	chr2:73929634-73929684	HCPEpiC	choroid plexus:	n/a
8	chr2:73929634-73929684	LNCaP	prostate:	n/a
9	chr2:73929634-73929684	T-47D	breast:	n/a
10	chr2:73929634-73929684	Caco-2	colon:	n/a
11	chr2:73929634-73929684	ProgFib	skin:	n/a
12	chr2:73929634-73929684	A549	lung:	n/a
13	chr2:73929634-73929684	HCF	heart:	n/a
14	chr2:73929634-73929684	HPAEpiC	pulmonary alveolar:	n/a
15	chr2:73929634-73929684	HEEpiC	esophagus:	n/a
16	chr2:73929634-73929684	Hela-S3	cervix:	n/a
17	chr2:73929634-73929684	GM12892	blood:	n/a
18	chr2:73929634-73929684	SAEC	small airway:	n/a
19	chr2:73929634-73929684	AoSMC	blood vessel:	n/a
20	chr2:73929634-73929684	Jurkat	blood:	n/a
21	chr2:73929634-73929684	GM12891	blood:	n/a
22	chr2:73929634-73929684	Hepatocyte	liver:	n/a
23	chr2:73929634-73929684	AG04450	lung:	fetal
24	chr2:73929634-73929684	MCF-7	breast:	n/a
25	chr2:73929634-73929684	ECC-1	luminal epithelium:	n/a
26	chr2:73929634-73929684	PrEC	prostate:	n/a
27	chr2:73929634-73929684	SK-N-SH_RA	brain:	n/a
28	chr2:73929634-73929684	U87	brain:	n/a
29	chr2:73929634-73929684	HNPCEpiC	eye:	n/a
30	chr2:73929634-73929684	AG09309	skin:	n/a
31	chr2:73929634-73929684	RPTEC	kidney:	n/a
32	chr2:73929634-73929684	IMR90	lung:	fetal
33	chr2:73929634-73929684	SK-N-MC	brain:	n/a
34	chr2:73929634-73929684	SK-N-SH	brain:	n/a
35	chr2:73929634-73929684	NT2-D1	testis:	n/a
36	chr2:73929634-73929684	SKMC	muscle:	n/a
37	chr2:73929634-73929684	H1-hESC	embryonic stem cell:	embryo
38	chr2:73929634-73929684	NHDF-neo	bronchial:	n/a
39	chr2:73929634-73929684	NH-A	brain:	n/a
40	chr2:73929634-73929684	HAEpiC	amniotic membrane:	n/a
41	chr2:73929634-73929684	K562	blood:	n/a
42	chr2:73929634-73929684	HEK293	kidney:	embryo
43	chr2:73929634-73929684	HCT-116	colon:	n/a
44	chr2:73929634-73929684	HepG2	liver:	n/a
45	chr2:73929634-73929684	PANC-1	pancreas:	n/a
46	chr2:73929634-73929684	HMEC	breast:	n/a
47	chr2:73929634-73929684	BE2_C	brain:	n/a
48	chr2:73929634-73929684	BJ	skin:	n/a
49	chr2:73929634-73929684	CMK	blood:	n/a
50	chr2:73929634-73929684	GM12878	blood:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:73868945..73872912-chr2:73927731..73932752,4	MCF-7	breast:
2	chr2:73920861..73923082-chr2:73929614..73932212,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000204872	TF binding region
ENSG00000204872	CpG island
ENSG00000163016	Chromatin interaction
ENSG00000144035	Chromatin interaction

Extended variants
information (count: 119 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs10172044	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10191988	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10200762	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10208995	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11126414	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11126415	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11126416	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11126417	0.83[EUR][1000 genomes]
rs11891140	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11892172	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11894953	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12052539	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12053242	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12233112	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12233115	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12611487	0.98[EUR][1000 genomes]
rs12615807	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12619258	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12624267	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12713788	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12713789	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12713790	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12713791	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12713793	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12713794	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12713795	0.86[EUR][1000 genomes]
rs12713797	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12713798	0.84[EUR][1000 genomes]
rs12992607	0.86[EUR][1000 genomes]
rs12997018	0.84[EUR][1000 genomes]
rs12997568	0.81[EUR][1000 genomes]
rs12998980	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13000788	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13003035	0.88[EUR][1000 genomes]
rs13005729	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13006448	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13013228	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13014700	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13015885	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13020517	0.83[EUR][1000 genomes]
rs13022837	0.84[EUR][1000 genomes]
rs13026192	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13031853	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13031866	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17350056	1.00[EUR][1000 genomes]
rs17350125	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17350188	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17434634	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17434655	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1806683	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1815028	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2001436	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2001490	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2006997	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2012574	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2116367	0.83[AMR][1000 genomes]
rs2272178	0.84[EUR][1000 genomes]
rs2421557	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2421558	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2421574	0.89[EUR][1000 genomes]
rs2421575	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2421672	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2421674	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2421675	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2421676	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2421677	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35421685	0.90[EUR][1000 genomes]
rs35498419	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35767294	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35791379	0.83[EUR][1000 genomes]
rs3980695	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4241257	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4358149	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4513320	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4852316	0.91[EUR][1000 genomes]
rs4852966	0.88[EUR][1000 genomes]
rs4852967	0.86[EUR][1000 genomes]
rs4852972	0.98[EUR][1000 genomes]
rs4852975	1.00[EUR][1000 genomes]
rs4852976	0.93[EUR][1000 genomes]
rs4852977	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4852978	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6732812	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6748233	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6749841	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6750494	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6750515	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6750877	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6755500	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7210	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7370393	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7558546	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7591112	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7599453	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7606947	0.90[EUR][1000 genomes]
rs7608328	0.84[EUR][1000 genomes]
rs891695	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9309475	0.83[EUR][1000 genomes]
rs9309476	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 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	nsv874275	chr2:73847024-73931971	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv874276	chr2:73847024-73964214	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
7	nsv874277	chr2:73870010-73931971	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv874278	chr2:73870010-73931971	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	esv3340115	chr2:73870416-73930142	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	esv3426494	chr2:73876125-73939153	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	esv3460808	chr2:73877074-73940302	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
12	esv3460809	chr2:73877074-73940302	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv829461	chr2:73877427-73931225	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	esv2753082	chr2:73891045-73955545	Weak transcription Bivalent Enhancer Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
15	nsv979022	chr2:73897805-73932073	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
16	esv34157	chr2:73901718-73949151	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
17	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
18	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
19	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
20	nsv1003153	chr2:73927235-73975416	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs4530394	ALMS1	Cis_1M	lymphoblastoid	RTeQTL
rs4530394	TPRKB	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73900600-73954800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr2:73902200-73931400	Weak transcription	Brain Anterior Caudate	brain
3	chr2:73926000-73931000	Enhancers	Fetal Intestine Small	intestine
4	chr2:73926200-73930600	Enhancers	Fetal Lung	lung
5	chr2:73926600-73929800	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr2:73926800-73929800	Enhancers	Stomach Mucosa	stomach
7	chr2:73927000-73930000	Enhancers	Ovary	ovary
8	chr2:73927000-73931400	Enhancers	Placenta	Placenta
9	chr2:73927200-73932600	Enhancers	Primary hematopoietic stem cells	blood
10	chr2:73927200-73932600	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr2:73927200-73932800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr2:73927600-73929800	Enhancers	Colonic Mucosa	Colon
13	chr2:73927600-73929800	Enhancers	Pancreas	Pancrea
14	chr2:73927800-73929800	Enhancers	Fetal Muscle Trunk	muscle
15	chr2:73927800-73930000	Enhancers	Lung	lung
16	chr2:73927800-73954800	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr2:73928000-73930200	Enhancers	Fetal Kidney	kidney
18	chr2:73928000-73930600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr2:73928200-73929800	Bivalent Enhancer	HUVEC	blood vessel
20	chr2:73928400-73929800	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr2:73928400-73929800	Enhancers	K562	blood
22	chr2:73928400-73930600	Weak transcription	Right Atrium	heart
23	chr2:73928400-73936200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr2:73928800-73929800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
25	chr2:73928800-73930000	Flanking Active TSS	Duodenum Mucosa	Duodenum
26	chr2:73929000-73929800	Enhancers	Esophagus	oesophagus
27	chr2:73929200-73929800	Enhancers	Spleen	Spleen
28	chr2:73929200-73930000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr2:73929200-73930800	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr2:73929200-73936400	Enhancers	Fetal Intestine Large	intestine
31	chr2:73929400-73929800	Flanking Active TSS	Liver	Liver
32	chr2:73929400-73929800	Bivalent Enhancer	Fetal Muscle Leg	muscle
33	chr2:73929400-73929800	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr2:73929400-73929800	Flanking Bivalent TSS/Enh	HepG2	liver
35	chr2:73929400-73930000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr2:73929400-73930200	Enhancers	Fetal Heart	heart
37	chr2:73929400-73931000	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr2:73929600-73929800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr2:73929600-73929800	Enhancers	Left Ventricle	heart
40	chr2:73929600-73930600	Weak transcription	Gastric	stomach
41	chr2:73929600-73930800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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