Variant report

Variant	rs11239929
Chromosome Location	chr1:146556093-146556094
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:478)
CpG islands
(count:0)
Chromatin interactive
region (count:87)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	PAX5	chr1:146555810-146556497	GM12878	blood:	n/a	n/a
2	ELF1	chr1:146556069-146556451	HepG2	liver:	n/a	chr1:146556320-146556332 chr1:146556313-146556322
3	RFX5	chr1:146555410-146556510	K562	blood:	n/a	n/a
4	JUND	chr1:146555809-146556886	K562	blood:	n/a	n/a
5	BCLAF1	chr1:146555663-146556579	GM12878	blood:	n/a	chr1:146556550-146556558
6	USF1	chr1:146555959-146556701	A549	lung:	n/a	n/a
7	BATF	chr1:146556062-146556384	GM12878	blood:	n/a	n/a
8	TCF7L2	chr1:146555541-146557042	Hela-S3	cervix:	n/a	n/a
9	SPI1	chr1:146556068-146556383	K562	blood:	n/a	n/a
10	SPI1	chr1:146556063-146556577	GM12878	blood:	n/a	n/a
11	SP1	chr1:146556092-146556591	HepG2	liver:	n/a	chr1:146556314-146556325
12	POLR2A	chr1:146556003-146556436	A549	lung:	n/a	n/a
13	SP1	chr1:146555855-146556777	A549	lung:	n/a	chr1:146556314-146556325
14	BCLAF1	chr1:146555399-146556726	K562	blood:	n/a	chr1:146556550-146556558
15	MAX	chr1:146555961-146556725	A549	lung:	n/a	n/a
16	POLR2A	chr1:146555537-146556803	HepG2	liver:	n/a	n/a
17	REST	chr1:146556093-146556354	K562	blood:	n/a	n/a
18	BCL3	chr1:146555779-146556405	GM12878	blood:	n/a	n/a
19	POLR2A	chr1:146555434-146557191	K562	blood:	n/a	n/a
20	POLR2A	chr1:146555467-146557086	K562	blood:	n/a	n/a
21	SIN3AK20	chr1:146555770-146556372	K562	blood:	n/a	n/a
22	POLR2A	chr1:146555353-146556785	IMR90	lung:	n/a	n/a
23	YY1	chr1:146556082-146556457	A549	lung:	n/a	n/a
24	MXI1	chr1:146555990-146556779	H1-hESC	embryonic stem cell:	n/a	n/a
25	EGR1	chr1:146556075-146556410	GM12878	blood:	n/a	n/a
26	POLR2A	chr1:146555822-146556676	HepG2	liver:	n/a	n/a
27	ETS1	chr1:146555987-146556351	A549	lung:	n/a	n/a
28	SIN3AK20	chr1:146555839-146556422	PFSK-1	brain:	n/a	n/a
29	TEAD4	chr1:146555962-146556595	A549	lung:	n/a	n/a
30	PML	chr1:146555558-146556838	GM12878	blood:	n/a	n/a
31	POLR2A	chr1:146555735-146556660	HL-60	blood:	n/a	n/a
32	GATA2	chr1:146555935-146556385	K562	blood:	n/a	n/a
33	ETS1	chr1:146555789-146556438	GM12878	blood:	n/a	n/a
34	ZNF143	chr1:146555935-146556735	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr1:146555477-146556685	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr1:146555481-146556767	GM18951	blood:	n/a	n/a
37	MAX	chr1:146555782-146556860	MCF-7	breast:	n/a	n/a
38	PAX5	chr1:146555794-146556656	GM12878	blood:	n/a	n/a
39	MEF2A	chr1:146555771-146556458	GM12878	blood:	n/a	chr1:146555831-146555846
40	CREB1	chr1:146555921-146556812	HepG2	liver:	n/a	n/a
41	EP300	chr1:146555960-146556469	GM12878	blood:	n/a	n/a
42	SP1	chr1:146555925-146556690	GM12878	blood:	n/a	chr1:146556314-146556325
43	POLR2A	chr1:146555520-146556849	GM12878	blood:	n/a	n/a
44	RDBP	chr1:146555360-146556389	K562	blood:	n/a	n/a
45	POU2F2	chr1:146555625-146556669	GM12878	blood:	n/a	n/a
46	ELF1	chr1:146555980-146556460	A549	lung:	n/a	chr1:146556320-146556332 chr1:146556313-146556322
47	BACH1	chr1:146555556-146556717	H1-hESC	embryonic stem cell:	n/a	n/a
48	BCL11A	chr1:146555603-146556714	GM12878	blood:	n/a	chr1:146556550-146556558
49	RUNX3	chr1:146555637-146556480	GM12878	blood:	n/a	n/a
50	RELA	chr1:146555755-146556576	GM12878	blood:	n/a	n/a

No data

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:146555688..146556591-chr10:75012122..75012630,2	Hela-S3	cervix:
2	chr1:146555480..146557423-chr1:146582452..146585260,2	MCF-7	breast:
3	chr1:146555582..146557721-chr16:70906703..70908588,2	MCF-7	breast:
4	chr1:146556050..146557611-chr16:70910877..70913228,2	K562	blood:
5	chr1:146555308..146557751-chr1:146572492..146574636,3	MCF-7	breast:
6	chr1:146555350..146556240-chr3:193852240..193853122,2	Hela-S3	cervix:
7	chr1:146554717..146557790-chr1:146713275..146715735,7	MCF-7	breast:
8	chr1:146555777..146556601-chr14:75745220..75746071,2	Hela-S3	cervix:
9	chr1:146555657..146558762-chr1:146628491..146630489,3	K562	blood:
10	chr1:146554322..146557448-chr1:146695605..146698369,3	K562	blood:
11	chr1:146554504..146557399-chr1:146713775..146716499,4	MCF-7	breast:
12	chr1:146553836..146557884-chr1:146641755..146644199,5	MCF-7	breast:
13	chr1:146555681..146556535-chr19:51307817..51308351,2	Hela-S3	cervix:
14	chr1:16840013..16841107-chr1:146555703..146556722,5	Hela-S3	cervix:
15	chr1:146555489..146556304-chr1:156697880..156698708,2	Hela-S3	cervix:
16	chr1:146555745..146557403-chr7:75933099..75935893,2	MCF-7	breast:
17	chr1:146555458..146558111-chr16:71130666..71132660,2	K562	blood:
18	chr1:146555685..146556600-chr12:46766325..46766994,2	Hela-S3	cervix:
19	chr1:146555822..146557545-chr1:146680381..146682107,2	K562	blood:
20	chr1:146555918..146556717-chr8:145064064..145064997,2	Hela-S3	cervix:
21	chr1:146555547..146556244-chr6:58778367..58779271,2	Hela-S3	cervix:
22	chr1:146554548..146558121-chr1:149223419..149225403,4	MCF-7	breast:
23	chr1:146555787..146556681-chr1:146628285..146629257,2	MCF-7	breast:
24	chr1:146555707..146556728-chr1:149223383..149224524,5	Hela-S3	cervix:
25	chr1:146554384..146557759-chr1:149221710..149225398,8	K562	blood:
26	chr1:146554522..146557720-chr1:147805011..147808218,6	K562	blood:
27	chr1:146555598..146556321-chr2:111435611..111436273,2	Hela-S3	cervix:
28	chr1:146554412..146557592-chr1:149221795..149226039,8	K562	blood:
29	chr1:146555833..146556576-chr2:149810062..149810583,2	Hela-S3	cervix:
30	chr1:146556000..146556597-chr1:149224593..149225521,2	Hela-S3	cervix:
31	chr1:146555778..146556576-chr11:82996663..82997528,2	Hela-S3	cervix:
32	chr1:146555982..146556682-chr1:146644129..146644630,2	Hela-S3	cervix:
33	chr1:146555785..146557578-chr1:146599828..146602177,2	MCF-7	breast:
34	chr1:146555134..146556670-chr1:146623816..146625708,2	K562	blood:
35	chr1:146555763..146556387-chr16:89626640..89627495,2	Hela-S3	cervix:
36	chr1:145382519..145383544-chr1:146555684..146556729,3	Hela-S3	cervix:
37	chr1:146555650..146556332-chr11:65194563..65195527,2	Hela-S3	cervix:
38	chr1:146556050..146556593-chr1:226250242..226250960,2	Hela-S3	cervix:
39	chr1:146555804..146556462-chr1:228327615..228328285,2	Hela-S3	cervix:
40	chr1:146555803..146556579-chr2:170654947..170655615,2	MCF-7	breast:
41	chr1:24069225..24069939-chr1:146555641..146556281,2	Hela-S3	cervix:
42	chr1:146555833..146557676-chr1:146673742..146675974,2	K562	blood:
43	chr1:110880956..110881459-chr1:146555893..146556631,2	Hela-S3	cervix:
44	chr1:146555811..146556515-chr17:49198284..49199134,2	Hela-S3	cervix:
45	chr1:146555629..146556415-chr5:134094109..134094676,2	Hela-S3	cervix:
46	chr1:146555569..146557322-chr1:146680607..146682552,2	K562	blood:
47	chr1:146550590..146559110-chr1:146711930..146718078,31	K562	blood:
48	chr1:146555502..146556485-chr21:35747301..35748035,3	Hela-S3	cervix:
49	chr1:146555730..146556321-chr7:158496940..158497729,2	Hela-S3	cervix:
50	chr1:146552515..146557737-chr1:146711619..146718083,31	K562	blood:

No data

Variant related genes	Relation type
ENSG00000230832	TF binding region
ENSG00000089006	Chromatin interaction
ENSG00000131781	Chromatin interaction
ENSG00000178719	Chromatin interaction
ENSG00000170345	Chromatin interaction
ENSG00000273071	Chromatin interaction
ENSG00000011007	Chromatin interaction
ENSG00000202408	Chromatin interaction
ENSG00000207005	Chromatin interaction
ENSG00000227242	Chromatin interaction
ENSG00000143774	Chromatin interaction
ENSG00000123473	Chromatin interaction
ENSG00000135486	Chromatin interaction
ENSG00000201699	Chromatin interaction
ENSG00000245750	Chromatin interaction
ENSG00000230524	Chromatin interaction
ENSG00000125871	Chromatin interaction
ENSG00000143303	Chromatin interaction
ENSG00000225555	Chromatin interaction
ENSG00000163041	Chromatin interaction
ENSG00000167526	Chromatin interaction
ENSG00000206652	Chromatin interaction
ENSG00000137500	Chromatin interaction
ENSG00000169679	Chromatin interaction
ENSG00000205670	Chromatin interaction
ENSG00000182180	Chromatin interaction
ENSG00000237188	Chromatin interaction
ENSG00000201558	Chromatin interaction
ENSG00000100554	Chromatin interaction
ENSG00000170832	Chromatin interaction
ENSG00000170634	Chromatin interaction
ENSG00000178685	Chromatin interaction
ENSG00000167747	Chromatin interaction
ENSG00000143319	Chromatin interaction
ENSG00000134001	Chromatin interaction
ENSG00000146918	Chromatin interaction
ENSG00000141371	Chromatin interaction
ENSG00000076382	Chromatin interaction
ENSG00000219807	Chromatin interaction
ENSG00000134294	Chromatin interaction
ENSG00000134250	Chromatin interaction
ENSG00000077514	Chromatin interaction
ENSG00000227543	Chromatin interaction
ENSG00000223316	Chromatin interaction
ENSG00000259248	Chromatin interaction
ENSG00000104419	Chromatin interaction
ENSG00000109536	Chromatin interaction
ENSG00000145833	Chromatin interaction
ENSG00000126091	Chromatin interaction
ENSG00000005020	Chromatin interaction
ENSG00000214413	Chromatin interaction
ENSG00000131778	Chromatin interaction
ENSG00000131791	Chromatin interaction
ENSG00000162775	Chromatin interaction
ENSG00000227540	Chromatin interaction
ENSG00000236200	Chromatin interaction
ENSG00000206737	Chromatin interaction
ENSG00000188529	Chromatin interaction
ENSG00000255234	Chromatin interaction
ENSG00000233030	Chromatin interaction
ENSG00000131375	Chromatin interaction
ENSG00000138385	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs11239936	1.00[ASW][hapmap];0.83[LWK][hapmap]
rs12074473	1.00[AFR][1000 genomes]
rs12078135	1.00[AFR][1000 genomes]
rs12081772	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12239852	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757753	chr1:145883119-146697542	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	nsv872251	chr1:146152553-146803630	Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
3	nsv872252	chr1:146471863-147398135	Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	112 gene(s)	inside rSNPs	diseases
4	nsv999546	chr1:146507577-147356574	Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
5	nsv535123	chr1:146507577-147356574	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
6	nsv492188	chr1:146507649-147381479	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
7	nsv916754	chr1:146507711-147417736	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats 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	113 gene(s)	inside rSNPs	diseases
8	nsv547673	chr1:146510112-147398135	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
9	nsv946298	chr1:146510432-146557539	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
10	nsv547674	chr1:146522722-147396797	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats 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	111 gene(s)	inside rSNPs	diseases
11	nsv998341	chr1:146531446-147384720	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
12	nsv535124	chr1:146531446-147384720	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats 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 miRNA target site	110 gene(s)	inside rSNPs	diseases
13	nsv1003493	chr1:146531446-147389944	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
14	nsv998209	chr1:146543722-147384720	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
15	nsv535126	chr1:146543722-147384720	Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
16	nsv872255	chr1:146550780-146969712	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	93 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:146555000-146557200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr1:146555000-146557200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
3	chr1:146555200-146556800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:146555200-146557200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
5	chr1:146555200-146557200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
6	chr1:146555200-146557400	Active TSS	HSMMtube	muscle
7	chr1:146555400-146556200	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
8	chr1:146555400-146556200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
9	chr1:146555400-146556200	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 31	rectum
10	chr1:146555400-146556600	Active TSS	NHEK	skin
11	chr1:146555400-146556800	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
12	chr1:146555400-146557000	Active TSS	Aorta	Aorta
13	chr1:146555400-146557000	Bivalent/Poised TSS	HepG2	liver
14	chr1:146555400-146557200	Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr1:146555400-146557200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
16	chr1:146555400-146557400	Bivalent/Poised TSS	A549	lung
17	chr1:146555400-146557400	Bivalent/Poised TSS	NHDF-Ad	bronchial
18	chr1:146555600-146556200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
19	chr1:146555600-146556200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
20	chr1:146555600-146556200	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
21	chr1:146555600-146556200	Flanking Bivalent TSS/Enh	Primary T killer naive cells fromperipheralblood	blood
22	chr1:146555600-146556200	Flanking Bivalent TSS/Enh	Colon Smooth Muscle	Colon
23	chr1:146555600-146556200	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
24	chr1:146555600-146556200	Flanking Bivalent TSS/Enh	Left Ventricle	heart
25	chr1:146555600-146556200	Active TSS	HMEC	breast
26	chr1:146555600-146556400	Bivalent/Poised TSS	Fetal Lung	lung
27	chr1:146555600-146556400	Flanking Active TSS	Placenta	Placenta
28	chr1:146555600-146556400	Bivalent/Poised TSS	Thymus	Thymus
29	chr1:146555600-146556600	Flanking Active TSS	Ovary	ovary
30	chr1:146555600-146556600	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
31	chr1:146555600-146556800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
32	chr1:146555600-146556800	Flanking Bivalent TSS/Enh	Primary mononuclear cells fromperipheralblood	Blood
33	chr1:146555600-146556800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
34	chr1:146555600-146557000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
35	chr1:146555600-146557000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr1:146555600-146557000	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr1:146555600-146557000	Flanking Active TSS	Adipose Nuclei	Adipose
38	chr1:146555600-146557000	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
39	chr1:146555600-146557000	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
40	chr1:146555600-146557000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
41	chr1:146555600-146557000	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
42	chr1:146555600-146557000	Active TSS	HSMM	muscle
43	chr1:146555600-146557000	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
44	chr1:146555600-146557200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr1:146555600-146557200	Active TSS	Breast Myoepithelial Primary Cells	Breast
46	chr1:146555600-146557200	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
47	chr1:146555600-146557200	Active TSS	Hela-S3	cervix
48	chr1:146555600-146557400	Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr1:146555600-146557400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:146555600-146557400	Bivalent/Poised TSS	Primary T cells from cord blood	blood

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