Variant report

Variant	rs16832249
Chromosome Location	chr1:45285048-45285049
allele	A/C
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:65)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:45283976..45287622-chr1:45450715..45458034,11	K562	blood:
2	chr1:45284408..45286561-chr17:56736164..56738109,2	K562	blood:
3	chr1:45203367..45205545-chr1:45283633..45285875,3	MCF-7	breast:
4	chr1:45284059..45286396-chr1:45450000..45452623,4	MCF-7	breast:
5	chr1:45284831..45285768-chr5:33441171..33441781,2	Hela-S3	cervix:
6	chr1:44496579..44498681-chr1:45284893..45286941,2	K562	blood:
7	chr1:45246681..45259677-chr1:45281336..45290057,25	MCF-7	breast:
8	chr1:45183794..45190315-chr1:45281186..45287888,32	MCF-7	breast:
9	chr1:45190324..45200952-chr1:45272085..45288310,59	MCF-7	breast:
10	chr1:45283441..45287322-chr1:45806283..45809735,5	K562	blood:
11	chr1:45196708..45197562-chr1:45284930..45285628,2	MCF-7	breast:
12	chr1:45282334..45285552-chr1:45442428..45444971,3	K562	blood:
13	chr1:45284063..45286769-chr1:45955098..45956816,2	K562	blood:
14	chr1:45284255..45286941-chr1:46048411..46051884,4	K562	blood:
15	chr1:45283791..45286747-chr1:45955379..45957255,3	MCF-7	breast:
16	chr1:45283844..45285860-chr1:45395492..45398129,3	K562	blood:
17	chr1:45265981..45266505-chr1:45284999..45285671,2	MCF-7	breast:
18	chr1:45210546..45213904-chr1:45284220..45286382,3	K562	blood:
19	chr1:45284967..45285500-chr12:7052719..7053484,2	NB4	blood:
20	chr1:45282564..45285374-chr1:45331380..45332950,2	K562	blood:
21	chr1:45284133..45286762-chr1:226249402..226251655,2	K562	blood:
22	chr1:28903771..28904376-chr1:45284977..45285526,2	Hela-S3	cervix:
23	chr1:44439015..44440810-chr1:45284320..45286959,2	MCF-7	breast:
24	chr1:45283510..45287262-chr1:45964108..45968951,6	K562	blood:
25	chr1:45282320..45290015-chr1:45470338..45482903,45	K562	blood:
26	chr1:45284971..45286641-chr17:56707765..56709298,2	MCF-7	breast:
27	chr1:11968061..11969967-chr1:45283683..45286236,2	MCF-7	breast:
28	chr1:45285019..45285694-chr11:68038866..68039629,2	Hela-S3	cervix:
29	chr1:45238319..45262026-chr1:45262351..45301953,358	K562	blood:
30	chr1:45283995..45285689-chr1:45985443..45988306,2	K562	blood:
31	chr1:45284581..45287931-chr1:45452240..45453906,3	MCF-7	breast:
32	chr1:45284750..45285585-chr20:50806892..50807827,2	Hela-S3	cervix:
33	chr1:45284131..45287086-chr1:46150918..46155233,4	K562	blood:
34	chr1:45285026..45285612-chr4:157157120..157157640,2	HCT-116	colon:
35	chr1:45193443..45200768-chr1:45280884..45289784,25	MCF-7	breast:
36	chr1:45282917..45288387-chr1:45449365..45456835,12	K562	blood:
37	chr1:45283391..45288738-chr1:46048072..46051277,6	K562	blood:
38	chr1:45282552..45286546-chr1:45802804..45805880,5	K562	blood:
39	chr1:45138628..45142139-chr1:45284311..45287293,3	K562	blood:
40	chr1:45284350..45286561-chr17:56735518..56737664,2	K562	blood:
41	chr1:45282552..45287322-chr1:45800975..45809178,15	K562	blood:
42	chr1:45265845..45266571-chr1:45284953..45285605,2	MCF-7	breast:
43	chr1:45282724..45285089-chr1:70684930..70687197,2	K562	blood:
44	chr1:45284268..45287037-chr1:45476110..45479807,4	MCF-7	breast:
45	chr1:45096122..45099489-chr1:45284877..45287072,3	K562	blood:
46	chr1:45284891..45287044-chr6:43595732..43598640,2	K562	blood:
47	chr1:45178001..45208867-chr1:45262751..45305400,520	K562	blood:
48	chr1:45283389..45288095-chr1:45474959..45480313,6	MCF-7	breast:
49	chr1:45284392..45287262-chr1:45964108..45967526,3	K562	blood:
50	chr1:45285005..45285733-chr16:2059329..2060039,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
ENSG00000198520	Chromatin interaction
ENSG00000196517	Chromatin interaction
ENSG00000199568	Chromatin interaction
ENSG00000273247	Chromatin interaction
ENSG00000111678	Chromatin interaction
ENSG00000264294	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000253039	Chromatin interaction
ENSG00000142937	Chromatin interaction
ENSG00000132780	Chromatin interaction
ENSG00000272562	Chromatin interaction
ENSG00000202031	Chromatin interaction
ENSG00000126088	Chromatin interaction
ENSG00000117450	Chromatin interaction
ENSG00000126106	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000234093	Chromatin interaction
ENSG00000124688	Chromatin interaction
ENSG00000117410	Chromatin interaction
ENSG00000225721	Chromatin interaction
ENSG00000172007	Chromatin interaction
ENSG00000132763	Chromatin interaction
ENSG00000172432	Chromatin interaction
ENSG00000200913	Chromatin interaction
ENSG00000132773	Chromatin interaction
ENSG00000236624	Chromatin interaction
ENSG00000206737	Chromatin interaction
ENSG00000159592	Chromatin interaction
ENSG00000200169	Chromatin interaction
ENSG00000199347	Chromatin interaction
ENSG00000183971	Chromatin interaction
ENSG00000070785	Chromatin interaction
ENSG00000199377	Chromatin interaction
ENSG00000207421	Chromatin interaction
ENSG00000238923	Chromatin interaction
ENSG00000187147	Chromatin interaction
ENSG00000167962	Chromatin interaction
ENSG00000132781	Chromatin interaction
ENSG00000268949	Chromatin interaction
ENSG00000173846	Chromatin interaction
ENSG00000172638	Chromatin interaction
ENSG00000228988	Chromatin interaction
ENSG00000113407	Chromatin interaction
ENSG00000070759	Chromatin interaction
ENSG00000171067	Chromatin interaction
ENSG00000162415	Chromatin interaction
ENSG00000142959	Chromatin interaction
ENSG00000163041	Chromatin interaction
ENSG00000232369	Chromatin interaction
ENSG00000142945	Chromatin interaction
ENSG00000159596	Chromatin interaction
ENSG00000203667	Chromatin interaction
ENSG00000116754	Chromatin interaction
ENSG00000126107	Chromatin interaction

Extended variants
information (count: 155 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:143)

rs_ID	r²[population]
rs10157761	0.81[EUR][1000 genomes]
rs10159318	0.90[EUR][1000 genomes]
rs10218751	0.80[EUR][1000 genomes]
rs1022814	0.82[EUR][1000 genomes]
rs1114390	0.84[EUR][1000 genomes]
rs11211042	0.93[CHB][hapmap];0.83[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11211043	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11211052	0.88[EUR][1000 genomes]
rs114833	0.89[EUR][1000 genomes]
rs12080887	0.88[EUR][1000 genomes]
rs12093313	0.89[EUR][1000 genomes]
rs12095412	0.93[CHB][hapmap];0.82[JPT][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12404127	0.85[EUR][1000 genomes]
rs12404160	0.83[EUR][1000 genomes]
rs12404168	0.87[EUR][1000 genomes]
rs12404244	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12405110	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12405721	0.82[EUR][1000 genomes]
rs12407290	0.80[EUR][1000 genomes]
rs12407565	0.82[EUR][1000 genomes]
rs12408763	0.93[EUR][1000 genomes]
rs12410088	0.86[EUR][1000 genomes]
rs12411070	0.86[EUR][1000 genomes]
rs13374816	0.87[EUR][1000 genomes]
rs1392035	0.84[EUR][1000 genomes]
rs1572379	0.89[EUR][1000 genomes]
rs1627320	0.86[EUR][1000 genomes]
rs16832251	0.93[CHB][hapmap];0.83[JPT][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16832301	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17390300	0.92[EUR][1000 genomes]
rs17390328	0.89[EUR][1000 genomes]
rs17390356	0.88[EUR][1000 genomes]
rs17390398	0.88[EUR][1000 genomes]
rs17390824	0.87[EUR][1000 genomes]
rs17390859	0.81[EUR][1000 genomes]
rs17390900	0.81[EUR][1000 genomes]
rs17390983	0.81[EUR][1000 genomes]
rs17392632	0.90[EUR][1000 genomes]
rs174636	0.88[EUR][1000 genomes]
rs17883304	0.80[EUR][1000 genomes]
rs17885815	0.81[EUR][1000 genomes]
rs2078329	0.84[EUR][1000 genomes]
rs2133501	0.87[EUR][1000 genomes]
rs2261859	0.80[EUR][1000 genomes]
rs2295996	0.92[CHB][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs263960	0.90[EUR][1000 genomes]
rs263961	0.89[EUR][1000 genomes]
rs263967	0.88[EUR][1000 genomes]
rs263971	0.89[EUR][1000 genomes]
rs263979	0.89[EUR][1000 genomes]
rs263981	0.86[EUR][1000 genomes]
rs264002	0.80[EUR][1000 genomes]
rs264004	0.80[EUR][1000 genomes]
rs264006	0.80[EUR][1000 genomes]
rs264007	0.80[EUR][1000 genomes]
rs28700974	0.82[EUR][1000 genomes]
rs28707013	0.82[EUR][1000 genomes]
rs28819230	0.80[EUR][1000 genomes]
rs35700678	0.89[EUR][1000 genomes]
rs371098	0.80[EUR][1000 genomes]
rs3738248	0.88[EUR][1000 genomes]
rs3767490	0.88[EUR][1000 genomes]
rs3795718	0.93[CHB][hapmap];0.83[JPT][hapmap];0.88[ASN][1000 genomes]
rs3889352	0.87[EUR][1000 genomes]
rs3889822	0.86[EUR][1000 genomes]
rs3923304	0.80[EUR][1000 genomes]
rs392410	0.89[EUR][1000 genomes]
rs4073112	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4082644	0.86[EUR][1000 genomes]
rs41269085	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs427392	0.80[EUR][1000 genomes]
rs435311	0.80[EUR][1000 genomes]
rs4415616	0.86[EUR][1000 genomes]
rs441876	0.80[EUR][1000 genomes]
rs4424549	0.87[EUR][1000 genomes]
rs4472791	0.86[EUR][1000 genomes]
rs4515833	0.86[EUR][1000 genomes]
rs4520451	0.83[EUR][1000 genomes]
rs4565758	0.80[EUR][1000 genomes]
rs471564	0.80[EUR][1000 genomes]
rs539409	0.80[EUR][1000 genomes]
rs546354	0.80[EUR][1000 genomes]
rs55708712	0.88[EUR][1000 genomes]
rs55756712	0.81[EUR][1000 genomes]
rs55792507	0.87[EUR][1000 genomes]
rs55807836	0.83[EUR][1000 genomes]
rs55851444	0.81[EUR][1000 genomes]
rs55893665	0.88[EUR][1000 genomes]
rs55916129	0.86[EUR][1000 genomes]
rs55926235	0.88[EUR][1000 genomes]
rs56102504	0.86[EUR][1000 genomes]
rs57104118	0.87[EUR][1000 genomes]
rs57769237	0.87[EUR][1000 genomes]
rs58191426	0.88[EUR][1000 genomes]
rs59050077	0.88[EUR][1000 genomes]
rs59552012	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs59559455	0.86[EUR][1000 genomes]
rs59803789	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59938994	0.88[EUR][1000 genomes]
rs60082006	0.81[EUR][1000 genomes]
rs606873	0.80[EUR][1000 genomes]
rs60741033	0.88[EUR][1000 genomes]
rs60766209	0.83[ASN][1000 genomes]
rs60787198	0.90[EUR][1000 genomes]
rs608649	0.88[EUR][1000 genomes]
rs61149327	0.90[EUR][1000 genomes]
rs61673889	0.82[EUR][1000 genomes]
rs637224	0.80[EUR][1000 genomes]
rs640743	0.80[EUR][1000 genomes]
rs6657078	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6678737	0.91[ASN][1000 genomes]
rs6684417	0.86[EUR][1000 genomes]
rs67058449	0.86[EUR][1000 genomes]
rs72674049	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72674051	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72674064	0.90[EUR][1000 genomes]
rs72674081	0.90[EUR][1000 genomes]
rs72674084	0.88[EUR][1000 genomes]
rs72676504	0.88[EUR][1000 genomes]
rs72676505	0.88[EUR][1000 genomes]
rs72676509	0.88[EUR][1000 genomes]
rs72676513	0.89[EUR][1000 genomes]
rs72676525	0.86[EUR][1000 genomes]
rs72676529	0.86[EUR][1000 genomes]
rs72676536	0.85[EUR][1000 genomes]
rs72676539	0.85[EUR][1000 genomes]
rs72676542	0.86[EUR][1000 genomes]
rs72676550	0.86[EUR][1000 genomes]
rs72676553	0.81[EUR][1000 genomes]
rs72676555	0.86[EUR][1000 genomes]
rs72676557	0.85[EUR][1000 genomes]
rs72676559	0.87[EUR][1000 genomes]
rs72676561	0.86[EUR][1000 genomes]
rs72676563	0.82[EUR][1000 genomes]
rs72676581	0.81[EUR][1000 genomes]
rs72677810	0.81[EUR][1000 genomes]
rs7515226	0.81[EUR][1000 genomes]
rs7519592	0.86[EUR][1000 genomes]
rs7529213	0.80[EUR][1000 genomes]
rs7529221	0.80[EUR][1000 genomes]
rs7531391	0.86[EUR][1000 genomes]
rs7533716	0.84[EUR][1000 genomes]
rs7546853	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533037	chr1:44361728-45333408	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	469 gene(s)	inside rSNPs	diseases
2	nsv998476	chr1:45001278-45311757	Flanking Active TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	426 gene(s)	inside rSNPs	diseases
3	nsv534941	chr1:45001278-45311757	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	426 gene(s)	inside rSNPs	diseases
4	nsv1014894	chr1:45139123-45397943	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	414 gene(s)	inside rSNPs	diseases
5	nsv529677	chr1:45179509-45748571	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	424 gene(s)	inside rSNPs	diseases
6	nsv1002026	chr1:45187594-45758048	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	386 gene(s)	inside rSNPs	diseases
7	nsv461406	chr1:45218542-45293518	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	127 gene(s)	inside rSNPs	diseases
8	nsv546145	chr1:45218542-45293518	Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	127 gene(s)	inside rSNPs	diseases
9	nsv870815	chr1:45233638-45318752	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	127 gene(s)	inside rSNPs	diseases
10	nsv546146	chr1:45258141-45318752	Genic enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	109 gene(s)	inside rSNPs	diseases
11	nsv870773	chr1:45259295-45287306	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	108 gene(s)	inside rSNPs	diseases
12	nsv915644	chr1:45282802-45696079	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45279800-45285600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:45279800-45285800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:45280800-45285200	Weak transcription	Esophagus	oesophagus
4	chr1:45281800-45285600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:45282800-45285200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:45284000-45285800	Weak transcription	Gastric	stomach
7	chr1:45284400-45285600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr1:45284600-45285200	Flanking Active TSS	Primary B cells from cord blood	blood
9	chr1:45284600-45285400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
10	chr1:45284600-45285600	Enhancers	HMEC	breast
11	chr1:45284600-45286600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
12	chr1:45284600-45287000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:45284800-45285200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:45284800-45285200	Flanking Active TSS	Primary B cells from peripheral blood	blood
15	chr1:45284800-45285200	Flanking Active TSS	Primary T cells from cord blood	blood
16	chr1:45284800-45285200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
17	chr1:45284800-45285200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
18	chr1:45284800-45285200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
19	chr1:45284800-45285200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
20	chr1:45284800-45285200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
21	chr1:45284800-45285200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
22	chr1:45284800-45285200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:45284800-45285200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
24	chr1:45284800-45285200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:45284800-45285200	Flanking Active TSS	Adipose Nuclei	Adipose
26	chr1:45284800-45285200	Flanking Active TSS	Liver	Liver
27	chr1:45284800-45285200	Flanking Active TSS	Brain Hippocampus Middle	brain
28	chr1:45284800-45285200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
29	chr1:45284800-45285200	Flanking Active TSS	Fetal Intestine Large	intestine
30	chr1:45284800-45285200	Flanking Active TSS	Fetal Intestine Small	intestine
31	chr1:45284800-45285200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
32	chr1:45284800-45285200	Flanking Active TSS	Stomach Mucosa	stomach
33	chr1:45284800-45285200	Flanking Active TSS	Stomach Smooth Muscle	stomach
34	chr1:45284800-45285200	Flanking Active TSS	GM12878-XiMat	blood
35	chr1:45284800-45285200	Flanking Active TSS	K562	blood
36	chr1:45284800-45285200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr1:45284800-45285200	Flanking Active TSS	NH-A	brain
38	chr1:45284800-45285200	Flanking Active TSS	NHDF-Ad	bronchial
39	chr1:45284800-45285200	Flanking Active TSS	Osteobl	bone
40	chr1:45284800-45285400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
41	chr1:45284800-45285400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr1:45284800-45285400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr1:45284800-45285400	Flanking Active TSS	HUVEC	blood vessel
44	chr1:45284800-45285400	Flanking Active TSS	NHEK	skin
45	chr1:45284800-45285600	Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr1:45284800-45285600	Active TSS	H1 Cell Line	embryonic stem cell
47	chr1:45284800-45285600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr1:45284800-45285600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr1:45284800-45285600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
50	chr1:45284800-45285600	Bivalent/Poised TSS	Brain Germinal Matrix	brain

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