Variant report

Variant	rs57378308
Chromosome Location	chr2:39348346-39348347
allele	A/G
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	HNF4A	chr2:39348033-39348828	HepG2	liver:	n/a	chr2:39348491-39348506 chr2:39348491-39348506 chr2:39348492-39348506
2	RAD21	chr2:39348057-39348365	SK-N-SH_RA	brain:	n/a	chr2:39348318-39348331
3	PML	chr2:39347885-39348558	MCF-7	breast:	n/a	n/a
4	SMARCB1	chr2:39346909-39348600	Hela-S3	cervix:	n/a	n/a
5	NR3C1	chr2:39347236-39348676	A549	lung:	n/a	chr2:39347716-39347729 chr2:39347607-39347620
6	CHD2	chr2:39347961-39348995	GM12878	blood:	n/a	n/a
7	ZMIZ1	chr2:39348057-39349288	K562	blood:	n/a	n/a
8	POLR2A	chr2:39347899-39348539	GM12892	blood:	n/a	n/a
9	YY1	chr2:39348007-39348397	GM12891	blood:	n/a	n/a
10	POLR2A	chr2:39347894-39348568	GM12892	blood:	n/a	n/a
11	MAX	chr2:39347901-39348760	A549	lung:	n/a	n/a
12	POLR2A	chr2:39347930-39348934	U87	brain:	n/a	n/a
13	HDAC2	chr2:39347973-39348748	HepG2	liver:	n/a	n/a
14	NR3C1	chr2:39348140-39348680	A549	lung:	n/a	n/a
15	MTA3	chr2:39347950-39349144	GM12878	blood:	n/a	n/a
16	POLR2A	chr2:39347884-39348688	SK-N-SH	brain:	n/a	n/a
17	NRF1	chr2:39348017-39348691	GM12878	blood:	n/a	chr2:39348192-39348203 chr2:39348189-39348203
18	FOXA2	chr2:39348153-39348868	HepG2	liver:	n/a	n/a
19	TAF1	chr2:39347218-39348728	HepG2	liver:	n/a	n/a
20	POLR2A	chr2:39347653-39348571	HEK293	kidney:	n/a	n/a
21	POLR2A	chr2:39347850-39348719	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr2:39346888-39348631	GM18951	blood:	n/a	n/a
23	FOXA1	chr2:39348058-39349040	HepG2	liver:	n/a	chr2:39348985-39348997
24	POLR2A	chr2:39347862-39348603	HUVEC	blood vessel:	n/a	n/a
25	POLR2A	chr2:39346877-39349041	Hela-S3	cervix:	n/a	n/a
26	YY1	chr2:39347868-39348480	H1-hESC	embryonic stem cell:	n/a	chr2:39347981-39347995 chr2:39347978-39347987 chr2:39347978-39347992
27	POLR2A	chr2:39347697-39348730	PFSK-1	brain:	n/a	n/a
28	POLR2A	chr2:39347951-39348459	GM12891	blood:	n/a	n/a
29	MAX	chr2:39346863-39348827	K562	blood:	n/a	chr2:39347262-39347272 chr2:39346924-39346934
30	POLR2A	chr2:39347925-39348686	GM12892	blood:	n/a	n/a
31	SIN3AK20	chr2:39347944-39348410	H1-hESC	embryonic stem cell:	n/a	n/a
32	FOXA1	chr2:39348086-39349141	HepG2	liver:	n/a	chr2:39348985-39348997
33	E2F4	chr2:39347423-39348548	K562	blood:	n/a	chr2:39347598-39347608 chr2:39347595-39347605 chr2:39347982-39347992
34	TAF1	chr2:39347845-39348560	H1-hESC	embryonic stem cell:	n/a	n/a
35	USF1	chr2:39347985-39348462	A549	lung:	n/a	chr2:39348021-39348037 chr2:39348027-39348043
36	POLR2A	chr2:39347902-39349025	SK-N-MC	brain:	n/a	n/a
37	TCF12	chr2:39348057-39348690	HepG2	liver:	n/a	chr2:39348324-39348334
38	POLR2A	chr2:39346749-39349066	H1-hESC	embryonic stem cell:	n/a	n/a
39	SIN3AK20	chr2:39346786-39348861	MCF-7	breast:	n/a	n/a
40	RCOR1	chr2:39347926-39348653	Hela-S3	cervix:	n/a	n/a
41	BCLAF1	chr2:39347949-39348528	GM12878	blood:	n/a	chr2:39348043-39348052 chr2:39347974-39347987 chr2:39348032-39348041
42	CREB1	chr2:39347844-39348560	A549	lung:	n/a	n/a
43	TAF1	chr2:39347998-39348383	PFSK-1	brain:	n/a	n/a
44	NFIC	chr2:39347925-39349284	HepG2	liver:	n/a	n/a
45	TEAD4	chr2:39348030-39348729	K562	blood:	n/a	n/a
46	REST	chr2:39347852-39348544	HL-60	blood:	n/a	chr2:39348312-39348332
47	POLR2A	chr2:39347852-39348542	A549	lung:	n/a	n/a
48	POLR2A	chr2:39347868-39348505	PANC-1	pancreas:	n/a	n/a
49	EP300	chr2:39348080-39348710	HepG2	liver:	n/a	chr2:39348491-39348501 chr2:39348327-39348343
50	TAF1	chr2:39347923-39348492	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:39346582..39349686-chr2:39454756..39458494,4	MCF-7	breast:
2	chr2:39319265..39325749-chr2:39345590..39349573,11	MCF-7	breast:
3	chr2:39346435..39348442-chr2:39355964..39358856,3	MCF-7	breast:
4	chr1:32109810..32110741-chr2:39347829..39348632,2	HCT-116	colon:
5	chr2:38975187..38978600-chr2:39347007..39351369,4	K562	blood:
6	chr2:38976457..38978515-chr2:39347011..39349138,2	K562	blood:
7	chr2:39233167..39234800-chr2:39347893..39350126,2	MCF-7	breast:
8	chr2:39347545..39348470-chr22:41842928..41843743,2	Hela-S3	cervix:
9	chr12:107349137..107350080-chr2:39347881..39348568,2	Hela-S3	cervix:
10	chr2:39348043..39352382-chr2:39450241..39456710,6	K562	blood:
11	chr15:91498077..91499009-chr2:39347881..39348578,2	Hela-S3	cervix:
12	chr11:43380983..43381940-chr2:39348218..39349084,2	NB4	blood:

Variant related genes	Relation type
SOS1	TF binding region
ENSG00000166965	Chromatin interaction
ENSG00000205111	Chromatin interaction
ENSG00000162517	Chromatin interaction
ENSG00000225900	Chromatin interaction
ENSG00000183864	Chromatin interaction
ENSG00000260329	Chromatin interaction
ENSG00000115904	Chromatin interaction
ENSG00000258384	Chromatin interaction
ENSG00000264078	Chromatin interaction
ENSG00000235790	Chromatin interaction
ENSG00000202309	Chromatin interaction
ENSG00000115875	Chromatin interaction
ENSG00000151135	Chromatin interaction

Extended variants
information (count: 117 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs10153761	0.95[EUR][1000 genomes]
rs10165968	0.89[EUR][1000 genomes]
rs10166801	0.93[EUR][1000 genomes]
rs10172085	0.93[EUR][1000 genomes]
rs10177250	0.84[EUR][1000 genomes]
rs10190377	0.84[EUR][1000 genomes]
rs10194374	0.93[EUR][1000 genomes]
rs10200058	0.83[EUR][1000 genomes]
rs10439459	0.95[EUR][1000 genomes]
rs11124659	0.95[EUR][1000 genomes]
rs11124660	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11692687	0.95[EUR][1000 genomes]
rs12620003	0.89[EUR][1000 genomes]
rs12620071	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12622969	0.87[EUR][1000 genomes]
rs12712630	0.81[EUR][1000 genomes]
rs13033392	0.84[EUR][1000 genomes]
rs1377860	0.98[EUR][1000 genomes]
rs1377861	0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1377863	0.95[EUR][1000 genomes]
rs1454220	0.81[EUR][1000 genomes]
rs1454226	0.95[EUR][1000 genomes]
rs1454227	0.82[EUR][1000 genomes]
rs1454228	0.89[EUR][1000 genomes]
rs1470914	0.82[EUR][1000 genomes]
rs1470915	0.95[EUR][1000 genomes]
rs1840281	0.89[EUR][1000 genomes]
rs2060989	0.98[EUR][1000 genomes]
rs2123876	0.91[EUR][1000 genomes]
rs2123879	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2123881	0.95[EUR][1000 genomes]
rs2123882	0.81[EUR][1000 genomes]
rs2168042	0.81[EUR][1000 genomes]
rs2373474	0.93[EUR][1000 genomes]
rs2373495	0.91[EUR][1000 genomes]
rs2373496	0.91[EUR][1000 genomes]
rs2888585	0.95[EUR][1000 genomes]
rs2924714	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2969763	0.98[EUR][1000 genomes]
rs297120	0.83[EUR][1000 genomes]
rs297121	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs297122	0.82[ASN][1000 genomes]
rs297124	0.84[EUR][1000 genomes]
rs297125	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs297127	0.81[EUR][1000 genomes]
rs297128	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs297129	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs297130	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs297131	0.86[EUR][1000 genomes]
rs297132	0.87[EUR][1000 genomes]
rs297133	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs297134	0.87[EUR][1000 genomes]
rs297135	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs297136	0.87[EUR][1000 genomes]
rs297137	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs297139	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs297140	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs297141	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs297142	0.87[EUR][1000 genomes]
rs297143	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs297144	0.84[EUR][1000 genomes]
rs297145	0.87[EUR][1000 genomes]
rs297147	0.87[EUR][1000 genomes]
rs297148	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs297149	0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs297150	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs297151	0.85[EUR][1000 genomes]
rs297152	0.85[EUR][1000 genomes]
rs297153	0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs297155	0.82[EUR][1000 genomes]
rs297156	0.85[EUR][1000 genomes]
rs297157	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs297158	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs297159	0.98[EUR][1000 genomes]
rs297161	0.84[EUR][1000 genomes]
rs366840	0.87[EUR][1000 genomes]
rs378698	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3796038	0.82[EUR][1000 genomes]
rs388958	0.87[EUR][1000 genomes]
rs4670272	0.91[EUR][1000 genomes]
rs4670905	0.98[EUR][1000 genomes]
rs58645871	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59732351	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61405040	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6419600	0.87[EUR][1000 genomes]
rs6544191	0.98[EUR][1000 genomes]
rs6544194	0.85[EUR][1000 genomes]
rs6544195	0.85[EUR][1000 genomes]
rs6544197	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6713281	0.95[EUR][1000 genomes]
rs6725356	0.93[EUR][1000 genomes]
rs6725644	0.93[EUR][1000 genomes]
rs6726833	0.84[EUR][1000 genomes]
rs6739568	0.81[EUR][1000 genomes]
rs6756184	0.91[EUR][1000 genomes]
rs72909662	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7568552	0.89[EUR][1000 genomes]
rs9309031	0.89[EUR][1000 genomes]
rs970409	0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs997344	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2755359	chr2:39169049-39417849	Strong transcription Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv873885	chr2:39200198-39573521	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv1010874	chr2:39255376-39604535	Strong transcription Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
4	nsv535649	chr2:39255376-39604535	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
5	nsv531346	chr2:39263225-39606367	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Genic 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	36 gene(s)	inside rSNPs	diseases
6	nsv533348	chr2:39264345-39596169	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
7	nsv1014520	chr2:39270598-39596299	Enhancers Active TSS Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
8	nsv535650	chr2:39270598-39596299	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
9	nsv1008198	chr2:39271472-39364035	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
10	nsv1009379	chr2:39271472-39604535	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
11	nsv581493	chr2:39277851-39547575	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
12	nsv581494	chr2:39277851-39626388	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
13	nsv533456	chr2:39281834-39596298	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
14	nsv581495	chr2:39282079-39475205	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
15	esv3495561	chr2:39346298-39349296	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
16	esv3495562	chr2:39346298-39349296	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	16 gene(s)	inside rSNPs	diseases
17	esv3326921	chr2:39346473-39349321	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs57378308	SOS1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:39344400-39348600	Active TSS	GM12878-XiMat	blood
2	chr2:39345200-39348800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr2:39345400-39348800	Active TSS	Ovary	ovary
4	chr2:39345400-39349200	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr2:39345600-39348400	Active TSS	HUES48 Cell Line	embryonic stem cell
6	chr2:39345600-39348600	Active TSS	Aorta	Aorta
7	chr2:39345800-39348600	Active TSS	Left Ventricle	heart
8	chr2:39345800-39348600	Active TSS	K562	blood
9	chr2:39345800-39348800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:39345800-39348800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
11	chr2:39345800-39348800	Active TSS	Colonic Mucosa	Colon
12	chr2:39346000-39348400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr2:39346000-39348400	Active TSS	Stomach Smooth Muscle	stomach
14	chr2:39346000-39348400	Active TSS	NHDF-Ad	bronchial
15	chr2:39346000-39348600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr2:39346000-39348600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr2:39346000-39348600	Active TSS	Sigmoid Colon	Sigmoid Colon
18	chr2:39346000-39348600	Active TSS	Small Intestine	intestine
19	chr2:39346000-39348600	Bivalent/Poised TSS	HepG2	liver
20	chr2:39346000-39348600	Active TSS	HMEC	breast
21	chr2:39346000-39348800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr2:39346000-39348800	Active TSS	HSMMtube	muscle
23	chr2:39346000-39349000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr2:39346000-39349000	Active TSS	Fetal Muscle Trunk	muscle
25	chr2:39346200-39348400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr2:39346200-39348400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:39346200-39348400	Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr2:39346200-39348400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
29	chr2:39346200-39348400	Active TSS	Primary T helper naive cells from peripheral blood	blood
30	chr2:39346200-39348400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr2:39346200-39348400	Active TSS	Primary T killer memory cells from peripheral blood	blood
32	chr2:39346200-39348400	Active TSS	Muscle Satellite Cultured Cells	--
33	chr2:39346200-39348400	Active TSS	Fetal Lung	lung
34	chr2:39346200-39348400	Active TSS	Placenta	Placenta
35	chr2:39346200-39348400	Active TSS	Rectal Mucosa Donor 29	rectum
36	chr2:39346200-39348400	Active TSS	Rectal Mucosa Donor 31	rectum
37	chr2:39346200-39348400	Active TSS	Thymus	Thymus
38	chr2:39346200-39348400	Active TSS	NHEK	skin
39	chr2:39346200-39348400	Active TSS	NHLF	lung
40	chr2:39346200-39348600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr2:39346200-39348600	Active TSS	Brain Cingulate Gyrus	brain
42	chr2:39346200-39348600	Active TSS	Duodenum Mucosa	Duodenum
43	chr2:39346200-39348600	Active TSS	Fetal Intestine Small	intestine
44	chr2:39346200-39348600	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr2:39346200-39348600	Active TSS	Fetal Muscle Leg	muscle
46	chr2:39346200-39348600	Active TSS	Stomach Mucosa	stomach
47	chr2:39346200-39348600	Active TSS	Hela-S3	cervix
48	chr2:39346200-39348600	Active TSS	Osteobl	bone
49	chr2:39346200-39348800	Active TSS	H9 Cell Line	embryonic stem cell
50	chr2:39346200-39348800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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