Variant report

Variant	rs12022027
Chromosome Location	chr1:228462896-228462897
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:16)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:16 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TEAD4	chr1:228462845-228463184	K562	blood:	n/a	n/a
2	RCOR1	chr1:228462777-228463320	K562	blood:	n/a	n/a
3	E2F6	chr1:228462892-228463855	K562	blood:	n/a	chr1:228463368-228463378
4	MAX	chr1:228462751-228464565	K562	blood:	n/a	chr1:228464133-228464140 chr1:228464032-228464041
5	RCOR1	chr1:228462777-228463986	K562	blood:	n/a	n/a
6	GABPA	chr1:228462884-228463413	H1-hESC	embryonic stem cell:	n/a	n/a
7	GABPA	chr1:228462787-228463430	H1-hESC	embryonic stem cell:	n/a	n/a
8	MAFF	chr1:228462848-228463009	K562	blood:	n/a	n/a
9	SPI1	chr1:228462807-228463038	K562	blood:	n/a	n/a
10	POLR2A	chr1:228462848-228462985	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr1:228462462-228464298	K562	blood:	n/a	n/a
12	ELF1	chr1:228462816-228463381	K562	blood:	n/a	chr1:228463333-228463345
13	ZNF143	chr1:228462836-228463150	K562	blood:	n/a	n/a
14	E2F6	chr1:228462866-228464538	K562	blood:	n/a	chr1:228463368-228463378
15	CBX3	chr1:228462674-228463970	K562	blood:	n/a	n/a
16	CTCF	chr1:228462860-228463010	HEK293	kidney:	n/a	n/a

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:228289703..228291795-chr1:228462279..228463838,2	K562	blood:
2	chr1:228353494..228355911-chr1:228462112..228465805,3	K562	blood:
3	chr1:228401876..228404808-chr1:228460949..228463356,3	K562	blood:
4	chr1:228399534..228402324-chr1:228461653..228463776,2	MCF-7	breast:
5	chr1:228395695..228398626-chr1:228460759..228464017,3	K562	blood:
6	chr1:228328463..228331528-chr1:228462308..228464210,3	K562	blood:
7	chr1:228461884..228463852-chr1:228571777..228574496,2	MCF-7	breast:
8	chr1:228461911..228467066-chr1:228644143..228647181,7	K562	blood:
9	chr1:228293306..228296150-chr1:228462712..228464969,2	K562	blood:
10	chr1:228326053..228331395-chr1:228462710..228467617,6	K562	blood:
11	chr1:228461911..228467066-chr1:228644125..228647181,7	K562	blood:
12	chr1:228351819..228355005-chr1:228461791..228464668,3	K562	blood:

No data

Variant related genes	Relation type
OBSCN	TF binding region
ENSG00000269890	TF binding region
ENSG00000181218	Chromatin interaction
ENSG00000181873	Chromatin interaction
ENSG00000196890	Chromatin interaction
ENSG00000203684	Chromatin interaction
ENSG00000162910	Chromatin interaction
ENSG00000270104	Chromatin interaction
ENSG00000143774	Chromatin interaction
ENSG00000162913	Chromatin interaction
ENSG00000154358	Chromatin interaction
ENSG00000143793	Chromatin interaction

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10916296	0.93[AMR][1000 genomes]
rs12022323	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12023522	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12023551	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12024329	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs12024368	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12025837	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs12026579	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs12028729	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs12028894	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12029540	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12029981	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12030528	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12031017	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12031390	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs12031747	1.00[AMR][1000 genomes]
rs12032850	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12032905	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12033588	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12033624	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12034508	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs12036437	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs12036485	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12037417	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs12037423	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs12037964	1.00[AMR][1000 genomes]
rs12038090	1.00[AMR][1000 genomes]
rs12038612	0.85[AMR][1000 genomes]
rs12039528	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs12040123	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12040394	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12040506	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs12041411	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs12042084	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs12043464	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12044918	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs12044962	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs12048283	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12049152	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs12049530	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12120597	1.00[AFR][1000 genomes]
rs2291999	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs2298013	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs28603121	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3754358	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs55760713	1.00[AMR][1000 genomes]
rs55946300	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56384735	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6693343	0.82[AMR][1000 genomes]
rs74144612	0.87[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv32853	chr1:227880116-228806209	Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases
2	nsv826908	chr1:227895386-228691100	Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
3	nsv523935	chr1:228038124-228681749	Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	137 gene(s)	inside rSNPs	diseases
4	nsv873253	chr1:228231601-228537942	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
5	nsv873254	chr1:228231601-228543800	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
6	nsv873255	chr1:228254753-228684779	Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Enhancers 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 miRNA miRNA target site	133 gene(s)	inside rSNPs	diseases
7	nsv827019	chr1:228314167-228651020	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	106 gene(s)	inside rSNPs	diseases
8	nsv1012078	chr1:228340876-228521843	Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	63 gene(s)	inside rSNPs	diseases
9	nsv535320	chr1:228340876-228521843	Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	63 gene(s)	inside rSNPs	diseases
10	nsv873263	chr1:228391808-228494790	Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
11	nsv873264	chr1:228423647-228543800	Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
12	nsv873265	chr1:228434395-228525008	Active TSS Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
13	nsv873266	chr1:228434395-228537942	Enhancers Strong transcription Weak transcription Genic 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	21 gene(s)	inside rSNPs	diseases
14	nsv873267	chr1:228434395-228585837	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers 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 miRNA target site	22 gene(s)	inside rSNPs	diseases
15	nsv873268	chr1:228442663-228537942	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
16	nsv873269	chr1:228442663-228543800	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
17	nsv873270	chr1:228442663-228699477	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
18	nsv1009891	chr1:228450763-228742676	Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
19	nsv873271	chr1:228450868-228470995	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
20	nsv873272	chr1:228450868-228538968	Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
21	nsv873273	chr1:228450868-228556788	Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
22	nsv873274	chr1:228450868-228585837	Strong transcription Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
23	esv1798020	chr1:228456147-228556788	Strong transcription Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
24	esv1818776	chr1:228456147-228556788	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
25	nsv873275	chr1:228456147-228585837	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
26	nsv517545	chr1:228456147-228685999	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
27	nsv873276	chr1:228456943-228585837	Weak transcription Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
28	nsv1013500	chr1:228459134-228849601	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
29	nsv827064	chr1:228459934-228469437	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228445000-228463200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:228447600-228463000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr1:228447800-228463000	Weak transcription	Psoas Muscle	Psoas
4	chr1:228450000-228463000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:228452400-228463000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr1:228455400-228484800	Weak transcription	A549	lung
7	chr1:228456400-228485800	Weak transcription	Hela-S3	cervix
8	chr1:228456600-228463200	Weak transcription	Aorta	Aorta
9	chr1:228457200-228472000	Weak transcription	Fetal Heart	heart
10	chr1:228459200-228463000	Strong transcription	Left Ventricle	heart
11	chr1:228459200-228463000	Weak transcription	HUVEC	blood vessel
12	chr1:228459400-228463000	Strong transcription	Fetal Intestine Small	intestine
13	chr1:228459400-228463000	Strong transcription	Thymus	Thymus
14	chr1:228459800-228463000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr1:228459800-228463000	Weak transcription	Right Atrium	heart
16	chr1:228459800-228469600	Weak transcription	HSMMtube	muscle
17	chr1:228460000-228463000	Weak transcription	Primary T cells from cord blood	blood
18	chr1:228460800-228463000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr1:228461000-228463000	Weak transcription	NHLF	lung
20	chr1:228461400-228463000	Weak transcription	Brain Cingulate Gyrus	brain
21	chr1:228461800-228463000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr1:228461800-228463400	Bivalent Enhancer	Placenta	Placenta
23	chr1:228462200-228463000	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr1:228462200-228463000	Enhancers	Pancreas	Pancrea
25	chr1:228462200-228463000	Enhancers	Placenta Amnion	Placenta Amnion
26	chr1:228462400-228463000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr1:228462400-228463000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr1:228462400-228463000	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr1:228462400-228463000	Genic enhancers	Fetal Muscle Trunk	muscle
30	chr1:228462400-228463000	Genic enhancers	Fetal Muscle Leg	muscle
31	chr1:228462400-228463000	Genic enhancers	Right Ventricle	heart
32	chr1:228462400-228463200	Enhancers	Gastric	stomach
33	chr1:228462400-228463200	Enhancers	Spleen	Spleen
34	chr1:228462400-228464200	Weak transcription	Dnd41	blood
35	chr1:228462600-228463000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
36	chr1:228462600-228463000	Enhancers	Primary B cells from cord blood	blood
37	chr1:228462600-228463000	Enhancers	Primary B cells from peripheral blood	blood
38	chr1:228462600-228463000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr1:228462600-228463000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr1:228462600-228463000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr1:228462600-228463000	Weak transcription	Fetal Intestine Large	intestine
42	chr1:228462600-228463000	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
43	chr1:228462600-228463400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr1:228462600-228463400	Flanking Active TSS	Stomach Smooth Muscle	stomach
45	chr1:228462600-228464400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr1:228462800-228463000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
47	chr1:228462800-228463000	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr1:228462800-228463000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr1:228462800-228463000	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr1:228462800-228463000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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