Variant report

Variant	rs10127448
Chromosome Location	chr1:45187511-45187512
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:567)
CpG islands
(count:0)
Chromatin interactive
region (count:160)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr1:45187215-45187672	H1-hESC	embryonic stem cell:	n/a	n/a
2	MYC	chr1:45187181-45187578	K562	blood:	n/a	n/a
3	SP1	chr1:45187042-45187817	K562	blood:	n/a	chr1:45187420-45187430
4	JUND	chr1:45187229-45187608	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr1:45187194-45187685	A549	lung:	n/a	n/a
6	POLR2A	chr1:45186525-45188188	GM12892	blood:	n/a	n/a
7	POLR2A	chr1:45186948-45187813	HUVEC	blood vessel:	n/a	n/a
8	ATF2	chr1:45187078-45187833	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr1:45186727-45187975	PANC-1	pancreas:	n/a	n/a
10	MYC	chr1:45186982-45188082	K562	blood:	n/a	chr1:45187887-45187897 chr1:45187921-45187931
11	ELF1	chr1:45187201-45187791	HepG2	liver:	n/a	n/a
12	STAT1	chr1:45187192-45188105	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr1:45186718-45188030	HepG2	liver:	n/a	n/a
14	CEBPD	chr1:45186690-45188067	K562	blood:	n/a	n/a
15	POLR2A	chr1:45187196-45187553	MCF-7	breast:	n/a	n/a
16	POLR2A	chr1:45186560-45188010	Hela-S3	cervix:	n/a	n/a
17	ZNF384	chr1:45186833-45187954	K562	blood:	n/a	n/a
18	SETDB1	chr1:45187217-45188077	U2OS	brain:	n/a	n/a
19	SIX5	chr1:45187199-45187655	K562	blood:	n/a	n/a
20	ETS1	chr1:45186710-45188052	K562	blood:	n/a	n/a
21	KAP1	chr1:45186979-45188054	U2OS	brain:	n/a	n/a
22	HDAC2	chr1:45187173-45187568	HepG2	liver:	n/a	n/a
23	SPI1	chr1:45187173-45187647	GM12891	blood:	n/a	n/a
24	TCF12	chr1:45187208-45187531	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr1:45187255-45187895	H1-hESC	embryonic stem cell:	n/a	n/a
26	REST	chr1:45187135-45187661	SK-N-SH	brain:	n/a	n/a
27	RELA	chr1:45186896-45188050	GM18951	blood:	n/a	n/a
28	TCF7L2	chr1:45187166-45187726	HCT-116	colon:	n/a	n/a
29	GATA3	chr1:45187144-45187748	MCF-7	breast:	n/a	n/a
30	CHD2	chr1:45186643-45187947	K562	blood:	n/a	n/a
31	MEF2A	chr1:45186955-45187704	K562	blood:	n/a	n/a
32	KAP1	chr1:45186744-45188041	HEK293	kidney:	n/a	n/a
33	POLR2A	chr1:45186579-45188023	K562	blood:	n/a	n/a
34	TCF12	chr1:45187180-45187703	HepG2	liver:	n/a	n/a
35	ZEB1	chr1:45187104-45187578	GM12878	blood:	n/a	n/a
36	USF1	chr1:45187180-45187754	A549	lung:	n/a	n/a
37	BACH1	chr1:45186691-45187799	K562	blood:	n/a	n/a
38	ZNF143	chr1:45187159-45187970	Hela-S3	cervix:	n/a	chr1:45187780-45187795
39	IRF1	chr1:45186886-45187917	K562	blood:	n/a	n/a
40	TAF1	chr1:45187190-45187634	GM12892	blood:	n/a	n/a
41	POLR2A	chr1:45186628-45188091	GM12891	blood:	n/a	n/a
42	REST	chr1:45187154-45187758	HepG2	liver:	n/a	n/a
43	PBX3	chr1:45187018-45187666	GM12878	blood:	n/a	n/a
44	USF1	chr1:45187158-45187683	A549	lung:	n/a	n/a
45	ZBTB33	chr1:45187024-45187701	K562	blood:	n/a	n/a
46	BCLAF1	chr1:45186672-45188044	GM12878	blood:	n/a	n/a
47	POLR2A	chr1:45187082-45187729	H1-hESC	embryonic stem cell:	n/a	n/a
48	KAT2A	chr1:45186906-45187742	Hela-S3	cervix:	n/a	n/a
49	EP300	chr1:45186873-45188097	K562	blood:	n/a	n/a
50	GTF2B	chr1:45186893-45188014	K562	blood:	n/a	n/a

No data

(count:160 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:45187216..45187887-chr1:45195575..45196869,4	MCF-7	breast:
2	chr1:45186750..45187594-chr3:51975747..51976594,2	HCT-116	colon:
3	chr1:45186606..45187940-chr16:82044607..82045675,4	HCT-116	colon:
4	chr1:45185360..45189158-chr1:210547543..210549064,10	K562	blood:
5	chr1:45187047..45187987-chr1:45196397..45197130,5	NB4	blood:
6	chr1:45185377..45188266-chr12:102512254..102513821,2	MCF-7	breast:
7	chr1:45186948..45187822-chr19:47249173..47249949,2	HCT-116	colon:
8	chr1:45186900..45187762-chr1:45265179..45266129,2	HCT-116	colon:
9	chr1:45186179..45189158-chr1:210547543..210549064,6	K562	blood:
10	chr1:45187059..45187775-chr15:78556309..78556823,2	Hela-S3	cervix:
11	chr1:45187257..45187784-chr1:150533689..150534335,2	Hela-S3	cervix:
12	chr1:45187087..45187940-chr7:100183318..100183872,2	Hela-S3	cervix:
13	chr1:45186902..45187591-chr8:71580726..71581504,2	Hela-S3	cervix:
14	chr1:45187081..45187830-chr9:140082854..140083677,2	HCT-116	colon:
15	chr1:45184334..45189303-chr1:45475138..45480545,18	K562	blood:
16	chr1:45185746..45188870-chr1:45307191..45310438,4	K562	blood:
17	chr1:45187494..45188388-chr12:57039227..57039857,2	HCT-116	colon:
18	chr1:45184712..45189957-chr1:45986029..45989344,7	K562	blood:
19	chr1:45095364..45099259-chr1:45185766..45189852,13	K562	blood:
20	chr1:45186891..45187821-chr4:10117955..10118566,2	NB4	blood:
21	chr1:45187283..45187917-chr1:45265572..45266144,2	Hela-S3	cervix:
22	chr1:45186864..45187549-chr16:74734613..74735470,2	Hela-S3	cervix:
23	chr1:45186671..45187949-chr1:45196091..45197272,8	Hela-S3	cervix:
24	chr1:45187055..45187570-chr2:9346941..9347890,2	Hela-S3	cervix:
25	chr1:45186988..45187776-chr12:125399953..125400850,2	Hela-S3	cervix:
26	chr1:45185419..45187569-chr19:13261567..13264440,2	K562	blood:
27	chr1:45185969..45188598-chr1:45964540..45967567,4	K562	blood:
28	chr1:11967939..11968694-chr1:45187030..45187930,3	HCT-116	colon:
29	chr1:45186675..45188755-chr1:45476881..45478812,3	MCF-7	breast:
30	chr1:45187068..45187795-chr11:82783098..82783818,2	Hela-S3	cervix:
31	chr1:45187410..45187928-chr17:48944824..48945523,2	Hela-S3	cervix:
32	chr1:45187018..45187769-chr1:160990629..160991569,2	NB4	blood:
33	chr1:45187006..45187713-chr19:39881563..39882073,2	Hela-S3	cervix:
34	chr1:45186798..45187678-chr17:43502939..43503458,2	HCT-116	colon:
35	chr1:45185754..45187905-chr1:46712528..46714563,2	K562	blood:
36	chr1:45186107..45187653-chr6:43737914..43739450,2	MCF-7	breast:
37	chr1:45186749..45187541-chr19:2475996..2476626,2	Hela-S3	cervix:
38	chr1:44479434..44482255-chr1:45185204..45188924,4	K562	blood:
39	chr1:45186971..45187547-chr16:87425850..87426376,2	Hela-S3	cervix:
40	chr1:45187108..45188095-chr2:74756333..74756877,2	NB4	blood:
41	chr1:45187271..45188987-chr1:144532926..144535604,2	K562	blood:
42	chr1:45186115..45188704-chr1:45270219..45273209,3	MCF-7	breast:
43	chr1:45187039..45187660-chr1:210547544..210548063,2	Hela-S3	cervix:
44	chr1:45186978..45187954-chr10:17659003..17659998,2	HCT-116	colon:
45	chr1:45186930..45187740-chr6:13814433..13814972,2	Hela-S3	cervix:
46	chr1:45187198..45188904-chr8:144688968..144691875,2	K562	blood:
47	chr1:45179633..45191596-chr1:45283435..45288613,20	MCF-7	breast:
48	chr1:45187196..45188979-chr1:148240047..148241581,2	MCF-7	breast:
49	chr1:45185285..45189072-chr1:45803209..45809453,10	K562	blood:
50	chr1:45187386..45188268-chr20:2632986..2633808,2	NB4	blood:

No data

Variant related genes	Relation type
C1orf228	TF binding region
ENSG00000181027	Chromatin interaction
ENSG00000151093	Chromatin interaction
ENSG00000230615	Chromatin interaction
ENSG00000117450	Chromatin interaction
ENSG00000187147	Chromatin interaction
ENSG00000071127	Chromatin interaction
ENSG00000168175	Chromatin interaction
ENSG00000033030	Chromatin interaction
ENSG00000142945	Chromatin interaction
ENSG00000232369	Chromatin interaction
ENSG00000116793	Chromatin interaction
ENSG00000161847	Chromatin interaction
ENSG00000204839	Chromatin interaction
ENSG00000198858	Chromatin interaction
ENSG00000168404	Chromatin interaction
ENSG00000143033	Chromatin interaction
ENSG00000139131	Chromatin interaction
ENSG00000168439	Chromatin interaction
ENSG00000255717	Chromatin interaction
ENSG00000176101	Chromatin interaction
ENSG00000101361	Chromatin interaction
ENSG00000237950	Chromatin interaction
ENSG00000132780	Chromatin interaction
ENSG00000199347	Chromatin interaction
ENSG00000259802	Chromatin interaction
ENSG00000163636	Chromatin interaction
ENSG00000257815	Chromatin interaction
ENSG00000110321	Chromatin interaction
ENSG00000114767	Chromatin interaction
ENSG00000151092	Chromatin interaction
ENSG00000126107	Chromatin interaction
ENSG00000253719	Chromatin interaction
ENSG00000184860	Chromatin interaction
ENSG00000197409	Chromatin interaction
ENSG00000090372	Chromatin interaction
ENSG00000201699	Chromatin interaction
ENSG00000041880	Chromatin interaction
ENSG00000137880	Chromatin interaction
ENSG00000147592	Chromatin interaction
ENSG00000135469	Chromatin interaction
ENSG00000105373	Chromatin interaction
ENSG00000160447	Chromatin interaction
ENSG00000196866	Chromatin interaction
ENSG00000050393	Chromatin interaction
ENSG00000126088	Chromatin interaction
ENSG00000200972	Chromatin interaction
ENSG00000116747	Chromatin interaction
ENSG00000233396	Chromatin interaction
ENSG00000175197	Chromatin interaction
ENSG00000164414	Chromatin interaction
ENSG00000077454	Chromatin interaction
ENSG00000188739	Chromatin interaction
ENSG00000125977	Chromatin interaction
ENSG00000110955	Chromatin interaction
ENSG00000188396	Chromatin interaction
ENSG00000152942	Chromatin interaction
ENSG00000064102	Chromatin interaction
ENSG00000166987	Chromatin interaction
ENSG00000200913	Chromatin interaction
ENSG00000145293	Chromatin interaction
ENSG00000159596	Chromatin interaction
ENSG00000129535	Chromatin interaction
ENSG00000246067	Chromatin interaction
ENSG00000049656	Chromatin interaction
ENSG00000140403	Chromatin interaction
ENSG00000116016	Chromatin interaction
ENSG00000201801	Chromatin interaction
ENSG00000132773	Chromatin interaction
ENSG00000197846	Chromatin interaction
ENSG00000105298	Chromatin interaction
ENSG00000226499	Chromatin interaction
ENSG00000183309	Chromatin interaction
ENSG00000116809	Chromatin interaction
ENSG00000224531	Chromatin interaction
ENSG00000107829	Chromatin interaction
ENSG00000159314	Chromatin interaction
ENSG00000104524	Chromatin interaction
ENSG00000160888	Chromatin interaction
ENSG00000111596	Chromatin interaction
ENSG00000258947	Chromatin interaction
ENSG00000225721	Chromatin interaction
ENSG00000196532	Chromatin interaction
ENSG00000198612	Chromatin interaction
ENSG00000169925	Chromatin interaction
ENSG00000204186	Chromatin interaction
ENSG00000138642	Chromatin interaction
ENSG00000110880	Chromatin interaction
ENSG00000266290	Chromatin interaction
ENSG00000246331	Chromatin interaction
ENSG00000270103	Chromatin interaction
ENSG00000112715	Chromatin interaction
ENSG00000265345	Chromatin interaction
ENSG00000198900	Chromatin interaction
ENSG00000129473	Chromatin interaction
ENSG00000178966	Chromatin interaction
ENSG00000176248	Chromatin interaction
ENSG00000127948	Chromatin interaction
ENSG00000222009	Chromatin interaction
ENSG00000116649	Chromatin interaction
ENSG00000110888	Chromatin interaction
ENSG00000075188	Chromatin interaction
ENSG00000006712	Chromatin interaction
ENSG00000196517	Chromatin interaction
ENSG00000272114	Chromatin interaction
ENSG00000173166	Chromatin interaction
ENSG00000259708	Chromatin interaction
ENSG00000163961	Chromatin interaction
ENSG00000177971	Chromatin interaction
ENSG00000132781	Chromatin interaction
ENSG00000165119	Chromatin interaction
ENSG00000116830	Chromatin interaction
ENSG00000132763	Chromatin interaction
ENSG00000070785	Chromatin interaction
ENSG00000085231	Chromatin interaction
ENSG00000117425	Chromatin interaction
ENSG00000207501	Chromatin interaction
ENSG00000221062	Chromatin interaction
ENSG00000158769	Chromatin interaction
ENSG00000201558	Chromatin interaction
ENSG00000099331	Chromatin interaction
ENSG00000198520	Chromatin interaction
ENSG00000099622	Chromatin interaction
ENSG00000200169	Chromatin interaction
ENSG00000116750	Chromatin interaction
ENSG00000117408	Chromatin interaction
ENSG00000265020	Chromatin interaction
ENSG00000101608	Chromatin interaction
ENSG00000168003	Chromatin interaction
ENSG00000158467	Chromatin interaction
ENSG00000063322	Chromatin interaction
ENSG00000111790	Chromatin interaction
ENSG00000203804	Chromatin interaction
ENSG00000165996	Chromatin interaction
ENSG00000006652	Chromatin interaction
ENSG00000260342	Chromatin interaction
ENSG00000264364	Chromatin interaction
ENSG00000264294	Chromatin interaction
ENSG00000115317	Chromatin interaction
ENSG00000142937	Chromatin interaction
ENSG00000140941	Chromatin interaction
ENSG00000236624	Chromatin interaction
ENSG00000095066	Chromatin interaction
ENSG00000172262	Chromatin interaction
ENSG00000102921	Chromatin interaction
ENSG00000257285	Chromatin interaction
ENSG00000100897	Chromatin interaction
ENSG00000255946	Chromatin interaction
ENSG00000258643	Chromatin interaction
ENSG00000124228	Chromatin interaction
ENSG00000166441	Chromatin interaction
ENSG00000159592	Chromatin interaction
ENSG00000170540	Chromatin interaction
ENSG00000085999	Chromatin interaction
ENSG00000236137	Chromatin interaction
ENSG00000137504	Chromatin interaction
ENSG00000159131	Chromatin interaction
ENSG00000196235	Chromatin interaction
ENSG00000141232	Chromatin interaction
ENSG00000173846	Chromatin interaction
ENSG00000152795	Chromatin interaction
ENSG00000111652	Chromatin interaction
ENSG00000182871	Chromatin interaction
ENSG00000246308	Chromatin interaction
ENSG00000117448	Chromatin interaction
ENSG00000131351	Chromatin interaction
ENSG00000115307	Chromatin interaction
ENSG00000202444	Chromatin interaction
ENSG00000099860	Chromatin interaction
ENSG00000143933	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10465818	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10890314	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11211027	0.93[AMR][1000 genomes]
rs11211030	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11211031	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11211034	0.83[ASN][1000 genomes]
rs11801067	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11808189	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11808852	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12094028	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12136048	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12136099	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12410588	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12742914	0.84[ASN][1000 genomes]
rs16832228	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4529751	0.80[ASN][1000 genomes]
rs4542248	0.87[EUR][1000 genomes]
rs6429548	0.88[EUR][1000 genomes]
rs6656337	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6658470	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6666987	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6671255	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6678729	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6685176	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6688710	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6693615	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7512710	0.90[ASN][1000 genomes]
rs7518836	0.86[ASN][1000 genomes]
rs7524446	0.90[EUR][1000 genomes]
rs7536146	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7550170	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7555065	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9988580	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[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	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	nsv1004861	chr1:44843654-45210176	Flanking Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	346 gene(s)	inside rSNPs	diseases
3	nsv534940	chr1:44843654-45210176	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	346 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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
7	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

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45174400-45190400	Weak transcription	Lung	lung
2	chr1:45181000-45187800	Weak transcription	Placenta	Placenta
3	chr1:45181200-45188800	Weak transcription	Liver	Liver
4	chr1:45181200-45194800	Weak transcription	Brain Anterior Caudate	brain
5	chr1:45183000-45187600	Enhancers	Primary T helper cells PMA-I stimulated	--
6	chr1:45183000-45188800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr1:45183000-45188800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr1:45183200-45189000	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr1:45184000-45187800	Weak transcription	Duodenum Mucosa	Duodenum
10	chr1:45184000-45189000	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr1:45184000-45189200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr1:45184000-45191000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:45184200-45188200	Weak transcription	Colonic Mucosa	Colon
14	chr1:45184200-45188800	Enhancers	GM12878-XiMat	blood
15	chr1:45184400-45187600	Enhancers	K562	blood
16	chr1:45184600-45188800	Enhancers	Primary T cells from cord blood	blood
17	chr1:45184600-45189000	Enhancers	Fetal Thymus	thymus
18	chr1:45184800-45188800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr1:45184800-45188800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr1:45184800-45189000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr1:45185000-45187600	Enhancers	Primary B cells from cord blood	blood
22	chr1:45185200-45187600	Weak transcription	Osteobl	bone
23	chr1:45185200-45189200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr1:45185200-45190600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr1:45185200-45192400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr1:45185400-45187800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr1:45185600-45192200	Weak transcription	NHDF-Ad	bronchial
28	chr1:45185600-45194800	Weak transcription	Dnd41	blood
29	chr1:45185800-45189000	Enhancers	Primary B cells from peripheral blood	blood
30	chr1:45186000-45188000	Enhancers	HepG2	liver
31	chr1:45186000-45188800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr1:45186000-45189600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr1:45186000-45190200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr1:45186200-45187800	Weak transcription	Spleen	Spleen
35	chr1:45186200-45192400	Weak transcription	HSMM	muscle
36	chr1:45186800-45188800	Enhancers	Primary hematopoietic stem cells	blood
37	chr1:45187000-45187800	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr1:45187000-45187800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr1:45187000-45188000	Active TSS	A549	lung
40	chr1:45187000-45188800	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr1:45187200-45187600	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr1:45187200-45187600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
43	chr1:45187200-45187600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr1:45187200-45187800	Bivalent/Poised TSS	Aorta	Aorta
45	chr1:45187200-45187800	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr1:45187200-45188000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr1:45187400-45187600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
48	chr1:45187400-45187800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
49	chr1:45187400-45187800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
50	chr1:45187400-45187800	Active TSS	Primary T killer memory cells from peripheral blood	blood

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