Variant report

Variant	rs398076004
Chromosome Location	chr11:67141490-67141491
allele	-/C
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	POLR2A	chr11:67141207-67142366	A549	lung:	n/a	n/a
2	TAF1	chr11:67141486-67141779	PFSK-1	brain:	n/a	n/a
3	POLR2A	chr11:67140056-67142142	SK-N-SH	brain:	n/a	n/a
4	EGR1	chr11:67141104-67141504	K562	blood:	n/a	chr11:67141407-67141417 chr11:67141364-67141377 chr11:67141366-67141376 chr11:67141244-67141258 chr11:67141243-67141256 chr11:67141363-67141378 chr11:67141364-67141377
5	EP300	chr11:67140889-67143973	A549	lung:	n/a	chr11:67141604-67141611 chr11:67143538-67143554 chr11:67140948-67140964 chr11:67141185-67141199
6	ZC3H11A	chr11:67141461-67141911	K562	blood:	n/a	n/a
7	SIX5	chr11:67140867-67142749	A549	lung:	n/a	chr11:67141928-67141937
8	MAX	chr11:67141380-67142614	A549	lung:	n/a	n/a
9	EP300	chr11:67141059-67142259	ECC-1	luminal epithelium:	n/a	chr11:67141604-67141611 chr11:67141185-67141199
10	MAX	chr11:67141410-67142269	MCF-7	breast:	n/a	n/a
11	SIN3AK20	chr11:67139835-67142256	MCF-7	breast:	n/a	n/a
12	POLR2A	chr11:67140037-67142665	Hela-S3	cervix:	n/a	n/a
13	ATF3	chr11:67141330-67142359	A549	lung:	n/a	chr11:67141369-67141378
14	PBX3	chr11:67140994-67142227	SK-N-SH	brain:	n/a	n/a
15	CREB1	chr11:67140861-67142257	A549	lung:	n/a	n/a
16	FOXA2	chr11:67141025-67142703	A549	lung:	n/a	chr11:67142411-67142423
17	HMGN3	chr11:67141352-67141920	K562	blood:	n/a	n/a
18	EP300	chr11:67140327-67143351	ECC-1	luminal epithelium:	n/a	chr11:67141604-67141611 chr11:67140948-67140964 chr11:67141185-67141199 chr11:67140686-67140702
19	SP1	chr11:67140841-67144091	A549	lung:	n/a	chr11:67143748-67143762 chr11:67141289-67141303 chr11:67141574-67141588 chr11:67141470-67141484 chr11:67141363-67141372 chr11:67141370-67141379 chr11:67141258-67141272 chr11:67141368-67141380 chr11:67140960-67140974 chr11:67140956-67140968 chr11:67143704-67143718 chr11:67141262-67141276 chr11:67143744-67143753 chr11:67141362-67141374 chr11:67142152-67142166 chr11:67141462-67141474 chr11:67142824-67142838 chr11:67140957-67140966 chr11:67142668-67142677 chr11:67143749-67143758 chr11:67141369-67141378 chr11:67141462-67141474 chr11:67140958-67140967 chr11:67141362-67141374 chr11:67141463-67141472 chr11:67141255-67141269 chr11:67142658-67142670 chr11:67142659-67142668 chr11:67142655-67142669 chr11:67142659-67142669 chr11:67141365-67141379 chr11:67141370-67141379 chr11:67143743-67143757 chr11:67141244-67141258 chr11:67141368-67141380 chr11:67142658-67142670 chr11:67140956-67140968
20	CEBPB	chr11:67140890-67142772	A549	lung:	n/a	n/a
21	TAF1	chr11:67141466-67141794	Hela-S3	cervix:	n/a	n/a
22	MAX	chr11:67141159-67142664	ECC-1	luminal epithelium:	n/a	chr11:67141256-67141266 chr11:67141367-67141377
23	POLR2A	chr11:67140101-67142367	HL-60	blood:	n/a	n/a
24	SP1	chr11:67141010-67143373	HCT-116	colon:	n/a	chr11:67141289-67141303 chr11:67141574-67141588 chr11:67141470-67141484 chr11:67141363-67141372 chr11:67141370-67141379 chr11:67141258-67141272 chr11:67141368-67141380 chr11:67141262-67141276 chr11:67141362-67141374 chr11:67142152-67142166 chr11:67141462-67141474 chr11:67142824-67142838 chr11:67142668-67142677 chr11:67141369-67141378 chr11:67141462-67141474 chr11:67141362-67141374 chr11:67141463-67141472 chr11:67141255-67141269 chr11:67142658-67142670 chr11:67142659-67142668 chr11:67142655-67142669 chr11:67142659-67142669 chr11:67141365-67141379 chr11:67141370-67141379 chr11:67141244-67141258 chr11:67141368-67141380 chr11:67142658-67142670
25	FOSL2	chr11:67141013-67142318	SK-N-SH	brain:	n/a	chr11:67141685-67141694 chr11:67141991-67142001 chr11:67141990-67142002 chr11:67141992-67142000 chr11:67141993-67142004 chr11:67141991-67142001 chr11:67141991-67142001
26	POLR2A	chr11:67140566-67142161	SK-N-SH	brain:	n/a	n/a
27	MAX	chr11:67140849-67144150	A549	lung:	n/a	chr11:67141256-67141266 chr11:67141367-67141377
28	RCOR1	chr11:67140534-67142921	IMR90	lung:	n/a	n/a
29	CREB1	chr11:67141469-67142007	A549	lung:	n/a	n/a
30	GATA3	chr11:67141489-67142239	SK-N-SH	brain:	n/a	n/a
31	FOSL2	chr11:67141350-67142231	MCF-7	breast:	n/a	chr11:67141685-67141694 chr11:67141991-67142001 chr11:67141990-67142002 chr11:67141992-67142000 chr11:67141993-67142004 chr11:67141991-67142001 chr11:67141991-67142001
32	NR3C1	chr11:67141026-67142250	A549	lung:	n/a	chr11:67141469-67141482 chr11:67141476-67141489 chr11:67141991-67142000 chr11:67141289-67141302 chr11:67141992-67142001
33	SIN3AK20	chr11:67141430-67142086	A549	lung:	n/a	n/a
34	CBX3	chr11:67141193-67142138	K562	blood:	n/a	n/a
35	CTBP2	chr11:67141454-67142097	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr11:67140087-67142126	K562	blood:	n/a	n/a
37	POLR2A	chr11:67140497-67142891	U87	brain:	n/a	n/a
38	NFIC	chr11:67141458-67142178	SK-N-SH	brain:	n/a	n/a
39	NR2F2	chr11:67141418-67142088	MCF-7	breast:	n/a	n/a
40	CHD2	chr11:67141284-67141529	K562	blood:	n/a	chr11:67141370-67141380
41	NR3C1	chr11:67141413-67142211	A549	lung:	n/a	chr11:67141469-67141482 chr11:67141476-67141489 chr11:67141991-67142000 chr11:67141992-67142001
42	HDAC2	chr11:67140997-67142519	MCF-7	breast:	n/a	chr11:67141185-67141199 chr11:67141186-67141200 chr11:67141148-67141162 chr11:67141149-67141163 chr11:67141150-67141164 chr11:67141184-67141198 chr11:67141187-67141201 chr11:67141182-67141196 chr11:67141188-67141202
43	ZNF263	chr11:67141375-67141965	HEK293-T-REx	kidney:	n/a	chr11:67141580-67141589 chr11:67141577-67141586 chr11:67141794-67141803
44	TEAD4	chr11:67140351-67141524	SK-N-SH	brain:	n/a	n/a
45	JUND	chr11:67141076-67142202	K562	blood:	n/a	chr11:67141685-67141694 chr11:67141991-67142001 chr11:67141990-67142002 chr11:67141990-67142001 chr11:67141992-67142000 chr11:67141993-67142004 chr11:67141991-67142001 chr11:67141991-67142001
46	HEY1	chr11:67141260-67142184	K562	blood:	n/a	chr11:67141412-67141427
47	POLR2A	chr11:67141366-67141832	HUVEC	blood vessel:	n/a	n/a
48	USF1	chr11:67141485-67142179	A549	lung:	n/a	chr11:67141758-67141769
49	ZBTB33	chr11:67141339-67142501	A549	lung:	n/a	n/a
50	CTCF	chr11:67141464-67142067	MCF-7	breast:	n/a	chr11:67141466-67141479

No.	Distal block	Cell Line	Cell type
1	chr11:67140365..67142235-chr11:67187974..67189991,2	K562	blood:
2	chr11:67140165..67142541-chr11:67273740..67276217,2	MCF-7	breast:
3	chr11:66821897..66826528-chr11:67139094..67144065,11	MCF-7	breast:
4	chr11:67031846..67035344-chr11:67139453..67142374,3	K562	blood:
5	chr11:67006828..67010582-chr11:67138867..67142453,4	MCF-7	breast:
6	chr1:110752769..110754407-chr11:67141303..67143426,2	MCF-7	breast:
7	chr11:67053474..67057507-chr11:67138689..67143945,8	MCF-7	breast:
8	chr11:67138872..67142169-chr11:67249496..67254071,4	MCF-7	breast:
9	chr11:67033933..67038277-chr11:67140224..67143646,5	MCF-7	breast:
10	chr11:67124080..67124985-chr11:67141333..67142050,4	K562	blood:
11	chr11:66788543..66790931-chr11:67139607..67141552,2	MCF-7	breast:
12	chr11:67069872..67072644-chr11:67140515..67142125,2	K562	blood:
13	chr11:66823034..66824892-chr11:67139520..67142366,3	MCF-7	breast:
14	chr11:67120355..67120891-chr11:67141344..67142247,2	MCF-7	breast:
15	chr11:67140268..67142517-chr20:55839534..55841832,2	MCF-7	breast:
16	chr11:67141172..67143536-chr11:67171363..67173683,2	K562	blood:
17	chr11:67139765..67142051-chr17:57918264..57920706,2	MCF-7	breast:
18	chr11:67137032..67142528-chr11:67234580..67238729,6	MCF-7	breast:
19	chr11:67140319..67142184-chr11:67395845..67397635,2	MCF-7	breast:
20	chr11:67006855..67009254-chr11:67139637..67141684,2	MCF-7	breast:
21	chr11:67077940..67083214-chr11:67140082..67142904,6	MCF-7	breast:
22	chr11:67140485..67142430-chr11:67273527..67275502,2	K562	blood:
23	chr11:67138430..67143112-chr11:67157518..67161987,7	K562	blood:
24	chr11:67139501..67142119-chr16:3071898..3074181,2	MCF-7	breast:
25	chr11:67070466..67072644-chr11:67139702..67142015,2	K562	blood:
26	chr11:67141166..67142111-chr16:30709540..30710323,2	Hela-S3	cervix:
27	chr11:67141217..67141721-chr15:65596618..65597187,2	Hela-S3	cervix:
28	chr11:67139623..67143035-chr11:67167894..67169679,3	K562	blood:
29	chr11:67140815..67142437-chr11:67396749..67399508,2	MCF-7	breast:
30	chr11:17098776..17099286-chr11:67140950..67141791,2	Hela-S3	cervix:
31	chr11:67055136..67057390-chr11:67140087..67141656,2	MCF-7	breast:
32	chr11:67140774..67143112-chr11:67157579..67159214,2	K562	blood:
33	chr11:67141217..67141794-chr9:139377418..139378330,2	Hela-S3	cervix:
34	chr11:67069246..67073295-chr11:67139634..67145393,8	MCF-7	breast:
35	chr11:67141283..67141790-chr7:106809496..106810341,2	Hela-S3	cervix:
36	chr11:67140134..67141664-chr11:67209999..67212449,2	K562	blood:
37	chr11:67140249..67142626-chr11:67380875..67383552,2	MCF-7	breast:
38	chr11:67078342..67081725-chr11:67139517..67143464,5	MCF-7	breast:
39	chr11:67030856..67037366-chr11:67138319..67144892,13	MCF-7	breast:
40	chr11:67116951..67127260-chr11:67135118..67146037,42	K562	blood:
41	chr11:67139414..67143301-chr11:67273275..67276817,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000256514	TF binding region
CLCF1	TF binding region
ENSG00000172531	Chromatin interaction
ENSG00000110700	Chromatin interaction
ENSG00000200156	Chromatin interaction
ENSG00000173156	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000173020	Chromatin interaction
ENSG00000172830	Chromatin interaction
ENSG00000172663	Chromatin interaction
ENSG00000110711	Chromatin interaction
ENSG00000172725	Chromatin interaction
ENSG00000116396	Chromatin interaction
ENSG00000175482	Chromatin interaction
ENSG00000196366	Chromatin interaction
ENSG00000103145	Chromatin interaction
ENSG00000167797	Chromatin interaction
ENSG00000172932	Chromatin interaction
ENSG00000231793	Chromatin interaction
ENSG00000173120	Chromatin interaction
ENSG00000261840	Chromatin interaction
ENSG00000175463	Chromatin interaction
ENSG00000131652	Chromatin interaction
ENSG00000172508	Chromatin interaction
ENSG00000105856	Chromatin interaction
ENSG00000110697	Chromatin interaction
ENSG00000172613	Chromatin interaction
ENSG00000101144	Chromatin interaction
ENSG00000167799	Chromatin interaction
ENSG00000173227	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv933183	chr11:67008447-67160993	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv897796	chr11:67021518-67186000	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers 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	103 gene(s)	inside rSNPs	diseases
4	nsv897797	chr11:67023040-67293234	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	206 gene(s)	inside rSNPs	diseases
5	nsv1043037	chr11:67027193-67357425	Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
6	nsv468603	chr11:67033076-67164495	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
7	nsv555253	chr11:67033076-67164495	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
8	nsv897801	chr11:67033076-67432479	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
9	nsv1047890	chr11:67058231-67184436	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
10	nsv1048230	chr11:67058231-67252397	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
11	nsv897804	chr11:67090571-67224278	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
12	nsv1039205	chr11:67135246-67252397	Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
13	esv1818769	chr11:67138811-67300457	Flanking Active TSS Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	167 gene(s)	inside rSNPs	diseases
14	esv3404685	chr11:67139076-67142024	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	38 gene(s)	inside rSNPs	diseases
15	esv3326147	chr11:67139201-67141749	Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	38 gene(s)	inside rSNPs	diseases
16	esv3323213	chr11:67139601-67142149	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	38 gene(s)	inside rSNPs	diseases
17	esv1798859	chr11:67139954-67272983	Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67136800-67143600	Bivalent Enhancer	Fetal Thymus	thymus
2	chr11:67139000-67141600	Active TSS	HSMMtube	muscle
3	chr11:67139200-67141600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
4	chr11:67139400-67141600	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr11:67139400-67141800	Active TSS	Fetal Kidney	kidney
6	chr11:67139400-67142000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:67139400-67142000	Active TSS	Muscle Satellite Cultured Cells	--
8	chr11:67139600-67141600	Active TSS	H9 Cell Line	embryonic stem cell
9	chr11:67139600-67141600	Active TSS	Sigmoid Colon	Sigmoid Colon
10	chr11:67139600-67141600	Active TSS	HSMM	muscle
11	chr11:67139600-67141600	Active TSS	Osteobl	bone
12	chr11:67139600-67141800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr11:67139600-67141800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr11:67139600-67142000	Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr11:67139600-67142000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr11:67139600-67142000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr11:67139600-67142000	Active TSS	Breast Myoepithelial Primary Cells	Breast
18	chr11:67139600-67142000	Active TSS	NHDF-Ad	bronchial
19	chr11:67139600-67142400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
20	chr11:67139800-67141600	Active TSS	HUES6 Cell Line	embryonic stem cell
21	chr11:67139800-67141600	Active TSS	Brain Substantia Nigra	brain
22	chr11:67139800-67141600	Active TSS	Fetal Lung	lung
23	chr11:67139800-67141600	Active TSS	Gastric	stomach
24	chr11:67139800-67141600	Active TSS	Left Ventricle	heart
25	chr11:67139800-67141600	Active TSS	HMEC	breast
26	chr11:67139800-67141600	Active TSS	NHLF	lung
27	chr11:67139800-67141800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
28	chr11:67139800-67141800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
29	chr11:67139800-67141800	Active TSS	Aorta	Aorta
30	chr11:67139800-67141800	Active TSS	Lung	lung
31	chr11:67139800-67142000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr11:67139800-67142000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr11:67139800-67142000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr11:67139800-67142000	Active TSS	A549	lung
35	chr11:67139800-67142200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr11:67140000-67141600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr11:67140000-67141600	Active TSS	Duodenum Smooth Muscle	Duodenum
38	chr11:67140000-67141600	Active TSS	Right Ventricle	heart
39	chr11:67140000-67141800	Active TSS	HUES64 Cell Line	embryonic stem cell
40	chr11:67140000-67141800	Active TSS	iPS-15b Cell Line	embryonic stem cell
41	chr11:67140200-67141800	Flanking Bivalent TSS/Enh	Dnd41	blood
42	chr11:67140200-67142200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:67140600-67141600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
44	chr11:67140600-67141600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr11:67140600-67141800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
46	chr11:67140600-67141800	Flanking Bivalent TSS/Enh	Thymus	Thymus
47	chr11:67140600-67142000	Flanking Active TSS	Primary B cells from cord blood	blood
48	chr11:67140600-67142000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
49	chr11:67140600-67142600	Bivalent Enhancer	Fetal Brain Male	brain
50	chr11:67140800-67142000	Flanking Active TSS	Primary hematopoietic stem cells	blood

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