Variant report

Variant	rs56275244
Chromosome Location	chr11:3863011-3863012
allele	G/T
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	MXI1	chr11:3861164-3863791	SK-N-SH	brain:	n/a	n/a
2	USF2	chr11:3862869-3863245	Hela-S3	cervix:	n/a	n/a
3	CTCF	chr11:3862829-3863069	A549	lung:	n/a	chr11:3862959-3862975 chr11:3862854-3862864 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
4	ATF2	chr11:3862451-3863240	GM12878	blood:	n/a	n/a
5	POLR2A	chr11:3860160-3863143	K562	blood:	n/a	n/a
6	CEBPB	chr11:3862966-3863072	H1-hESC	embryonic stem cell:	n/a	n/a
7	EGR1	chr11:3861895-3863100	K562	blood:	n/a	chr11:3862477-3862490 chr11:3862844-3862857 chr11:3862811-3862821 chr11:3862805-3862820 chr11:3862943-3862953 chr11:3862048-3862057 chr11:3862474-3862488 chr11:3862017-3862027 chr11:3862806-3862819 chr11:3862312-3862325 chr11:3862294-3862304 chr11:3862806-3862819 chr11:3862477-3862487 chr11:3862808-3862818
8	JUND	chr11:3861962-3863103	A549	lung:	n/a	chr11:3862182-3862191
9	CTCF	chr11:3862960-3863110	GM12801	blood:	n/a	chr11:3862960-3862973 chr11:3862961-3862971
10	CTCF	chr11:3862838-3863091	MCF-7	breast:	n/a	chr11:3862959-3862975 chr11:3862854-3862864 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
11	JUN	chr11:3862523-3863093	K562	blood:	n/a	n/a
12	TCF12	chr11:3862697-3863053	GM12878	blood:	n/a	n/a
13	REST	chr11:3862712-3863129	PFSK-1	brain:	n/a	chr11:3862772-3862786 chr11:3862783-3862796
14	POLR2A	chr11:3861928-3863086	HEK293	kidney:	n/a	n/a
15	CTCF	chr11:3862841-3863107	MCF-7	breast:	n/a	chr11:3862959-3862975 chr11:3862854-3862864 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
16	POU2F2	chr11:3862253-3863181	GM12878	blood:	n/a	chr11:3862282-3862294 chr11:3862808-3862820 chr11:3862848-3862860 chr11:3862479-3862491
17	CTCF	chr11:3862920-3863070	HL-60	blood:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
18	TAF1	chr11:3862772-3863191	PFSK-1	brain:	n/a	n/a
19	CTCF	chr11:3862880-3863030	AG04450	lung:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
20	CTCF	chr11:3862880-3863030	HEK293	kidney:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
21	MAFK	chr11:3862679-3863159	HepG2	liver:	n/a	chr11:3862683-3862700
22	ELF1	chr11:3862794-3863170	A549	lung:	n/a	n/a
23	MAZ	chr11:3860356-3863182	GM12878	blood:	n/a	chr11:3862304-3862314 chr11:3862809-3862819 chr11:3862477-3862487 chr11:3862016-3862026
24	WRNIP1	chr11:3862888-3863218	GM12878	blood:	n/a	n/a
25	CTCF	chr11:3862900-3863050	HVMF	connective:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
26	TFAP2A	chr11:3862443-3863100	Hela-S3	cervix:	n/a	chr11:3862598-3862606 chr11:3862598-3862606 chr11:3862596-3862611 chr11:3862598-3862606
27	CTCF	chr11:3862880-3863030	HRE	kidney:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
28	RAD21	chr11:3862781-3863166	A549	lung:	n/a	chr11:3862958-3862970 chr11:3862959-3862972 chr11:3862956-3862975 chr11:3862962-3862971
29	EP300	chr11:3862339-3863219	K562	blood:	n/a	n/a
30	POLR2A	chr11:3861619-3863157	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr11:3861415-3863095	GM15510	blood:	n/a	n/a
32	CTCF	chr11:3862900-3863050	GM12867	blood:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
33	SIN3AK20	chr11:3862820-3863152	HepG2	liver:	n/a	n/a
34	CTCF	chr11:3862730-3863226	MCF-7	breast:	n/a	chr11:3862959-3862975 chr11:3862854-3862864 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
35	EBF1	chr11:3862314-3863024	GM12878	blood:	n/a	chr11:3862698-3862708 chr11:3862544-3862553 chr11:3862648-3862659 chr11:3862698-3862707
36	MAX	chr11:3862290-3863241	K562	blood:	n/a	chr11:3862304-3862314 chr11:3862809-3862819 chr11:3862477-3862487
37	CTCF	chr11:3862900-3863050	HBMEC	blood vessel:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
38	CTCF	chr11:3862880-3863030	AG10803	skin:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
39	CTCF	chr11:3862960-3863110	HCT-116	colon:	n/a	chr11:3862960-3862973 chr11:3862961-3862971
40	RCOR1	chr11:3862473-3863386	GM12878	blood:	n/a	n/a
41	CTCF	chr11:3862667-3863199	K562	blood:	n/a	chr11:3862959-3862975 chr11:3862854-3862864 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
42	CTCF	chr11:3862920-3863070	Hela-S3	cervix:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
43	MAX	chr11:3860293-3863282	NB4	blood:	n/a	chr11:3862304-3862314 chr11:3862809-3862819 chr11:3862477-3862487 chr11:3862016-3862026
44	POLR2A	chr11:3860236-3863236	GM19099	blood:	n/a	n/a
45	NFIC	chr11:3862359-3863251	GM12878	blood:	n/a	n/a
46	YY1	chr11:3862469-3863134	GM12892	blood:	n/a	chr11:3862811-3862820
47	CTCF	chr11:3862920-3863070	GM12872	blood:	n/a	chr11:3862959-3862975 chr11:3862960-3862973 chr11:3862961-3862971 chr11:3862958-3862976
48	ARID3A	chr11:3862890-3863079	K562	blood:	n/a	n/a
49	SP4	chr11:3862781-3863097	H1-hESC	embryonic stem cell:	n/a	chr11:3862806-3862822 chr11:3862808-3862824 chr11:3862939-3862955
50	GABPA	chr11:3861769-3863058	K562	blood:	n/a	chr11:3862811-3862820 chr11:3862046-3862055 chr11:3862295-3862304

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:3862991-3863041	SK-N-SH	brain:	n/a
2	chr11:3862991-3863041	NH-A	brain:	n/a
3	chr11:3862991-3863041	SAEC	small airway:	n/a
4	chr11:3862991-3863041	AG04449	skin:	fetal
5	chr11:3862991-3863041	HRPEpiC	eye:	n/a
6	chr11:3862991-3863041	HNPCEpiC	eye:	n/a
7	chr11:3862991-3863041	HMEC	breast:	n/a
8	chr11:3862991-3863041	HUVEC	blood vessel:	n/a
9	chr11:3862991-3863041	HAEpiC	amniotic membrane:	n/a
10	chr11:3862991-3863041	H1-hESC	embryonic stem cell:	embryo
11	chr11:3862991-3863041	HEEpiC	esophagus:	n/a
12	chr11:3862991-3863041	Hela-S3	cervix:	n/a
13	chr11:3862991-3863041	T-47D	breast:	n/a
14	chr11:3862991-3863041	Jurkat	blood:	n/a
15	chr11:3862991-3863041	SKMC	muscle:	n/a
16	chr11:3862991-3863041	BE2_C	brain:	n/a
17	chr11:3862991-3863041	GM12892	blood:	n/a
18	chr11:3862991-3863041	AG09309	skin:	n/a
19	chr11:3862991-3863041	AG04450	lung:	fetal
20	chr11:3862991-3863041	GM19239	blood:	n/a
21	chr11:3862991-3863041	GM12891	blood:	n/a
22	chr11:3862991-3863041	MCF-7	breast:	n/a
23	chr11:3862991-3863041	U87	brain:	n/a
24	chr11:3862991-3863041	BJ	skin:	n/a
25	chr11:3862991-3863041	GM12878	blood:	n/a
26	chr11:3862991-3863041	K562	blood:	n/a
27	chr11:3862991-3863041	HPAEpiC	pulmonary alveolar:	n/a
28	chr11:3862991-3863041	IMR90	lung:	fetal
29	chr11:3862991-3863041	A549	lung:	n/a
30	chr11:3862991-3863041	ProgFib	skin:	n/a
31	chr11:3862991-3863041	MCF10A-Er-Src	breast:	n/a
32	chr11:3862991-3863041	LNCaP	prostate:	n/a
33	chr11:3862991-3863041	PANC-1	pancreas:	n/a
34	chr11:3862991-3863041	NT2-D1	testis:	n/a
35	chr11:3862991-3863041	HIPEpiC	eye:	n/a
36	chr11:3862991-3863041	PrEC	prostate:	n/a
37	chr11:3862991-3863041	HL-60	blood:	n/a
38	chr11:3862991-3863041	NHBE	bronchial:	n/a
39	chr11:3862991-3863041	Caco-2	colon:	n/a
40	chr11:3862991-3863041	HRCEpiC	kidney:	n/a
41	chr11:3862991-3863041	SK-N-MC	brain:	n/a
42	chr11:3862991-3863041	SK-N-SH_RA	brain:	n/a
43	chr11:3862991-3863041	NB4	blood:	n/a
44	chr11:3862991-3863041	HepG2	liver:	n/a
45	chr11:3862991-3863041	HCM	heart:	n/a
46	chr11:3862991-3863041	PFSK-1	brain:	n/a
47	chr11:3862991-3863041	AoSMC	blood vessel:	n/a
48	chr11:3862991-3863041	HCPEpiC	choroid plexus:	n/a
49	chr11:3862991-3863041	ECC-1	luminal epithelium:	n/a
50	chr11:3862991-3863041	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:3862483..3865232-chr11:3890007..3892959,2	K562	blood:
2	chr11:3861720..3863854-chr11:3876323..3877978,2	MCF-7	breast:
3	chr11:3858623..3864245-chr11:3874959..3879217,11	K562	blood:
4	chr11:3815959..3820545-chr11:3854514..3864703,12	K562	blood:
5	chr11:3817048..3820526-chr11:3859691..3864703,8	K562	blood:
6	chr11:3862990..3867083-chr11:3867871..3871459,5	K562	blood:
7	chr11:3857497..3860664-chr11:3860718..3863734,5	MCF-7	breast:
8	chr11:3862693..3864773-chr11:4060192..4062998,2	MCF-7	breast:
9	chr11:3862793..3864567-chr11:4100746..4102871,2	K562	blood:
10	chr11:3861261..3864016-chr11:3874431..3876289,3	MCF-7	breast:
11	chr11:3842483..3845464-chr11:3861552..3863945,2	MCF-7	breast:
12	chr11:3845241..3847374-chr11:3862493..3863741,9	K562	blood:
13	chr11:3845748..3846401-chr11:3862699..3863275,2	MCF-7	breast:
14	chr11:3827764..3831807-chr11:3860648..3864124,7	K562	blood:
15	chr11:3861239..3864353-chr11:4095380..4099458,3	MCF-7	breast:
16	chr11:3862506..3865244-chr11:4006779..4008318,2	K562	blood:
17	chr11:3860189..3865275-chr11:3872883..3879283,10	K562	blood:
18	chr11:3829046..3832201-chr11:3860687..3864518,3	MCF-7	breast:
19	chr11:3861564..3863892-chr11:4106134..4108924,2	MCF-7	breast:

Variant related genes	Relation type
RHOG	TF binding region
RHOG	CpG island
ENSG00000229368	Chromatin interaction
ENSG00000263421	Chromatin interaction
ENSG00000228661	Chromatin interaction
ENSG00000177105	Chromatin interaction
ENSG00000110713	Chromatin interaction
ENSG00000148985	Chromatin interaction
ENSG00000167323	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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	nsv1049560	chr11:3678259-3980746	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv540907	chr11:3678259-3980746	Weak transcription Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv1052744	chr11:3739162-4017601	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats 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	29 gene(s)	inside rSNPs	diseases
4	nsv1047025	chr11:3750969-4017601	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	esv1803195	chr11:3806490-3924156	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
6	nsv1046065	chr11:3808818-4049150	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
7	nsv540909	chr11:3808818-4049150	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
8	nsv1046325	chr11:3856201-3895148	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
9	nsv1039059	chr11:3856201-3909415	Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
10	nsv540910	chr11:3856201-3909415	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
11	nsv1051580	chr11:3856201-3924216	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
12	nsv1043265	chr11:3856201-3926407	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
13	nsv896894	chr11:3859856-3888234	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
14	esv3325772	chr11:3860901-3863749	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
15	esv3479108	chr11:3861476-3863424	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
16	esv3479119	chr11:3861476-3863424	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:3860600-3863200	Active TSS	Colonic Mucosa	Colon
2	chr11:3860800-3863200	Active TSS	iPS-20b Cell Line	embryonic stem cell
3	chr11:3861000-3863200	Active TSS	H9 Cell Line	embryonic stem cell
4	chr11:3861200-3863200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr11:3861200-3863200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr11:3861200-3863200	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr11:3861400-3863200	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr11:3861400-3863200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr11:3861400-3863200	Active TSS	Duodenum Smooth Muscle	Duodenum
10	chr11:3861400-3863200	Active TSS	Small Intestine	intestine
11	chr11:3861600-3863200	Active TSS	H1 Cell Line	embryonic stem cell
12	chr11:3861600-3863200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr11:3861600-3863200	Active TSS	HUES6 Cell Line	embryonic stem cell
14	chr11:3861600-3863200	Active TSS	Breast Myoepithelial Primary Cells	Breast
15	chr11:3861600-3863200	Active TSS	Brain Cingulate Gyrus	brain
16	chr11:3861600-3863400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
17	chr11:3861600-3863400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr11:3861600-3863400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr11:3861800-3863200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr11:3861800-3863200	Active TSS	Liver	Liver
21	chr11:3861800-3863200	Active TSS	Brain Germinal Matrix	brain
22	chr11:3861800-3863400	Active TSS	Fetal Brain Female	brain
23	chr11:3862000-3863200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr11:3862400-3863400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
25	chr11:3862600-3863200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr11:3862600-3863200	Flanking Active TSS	HMEC	breast
27	chr11:3862800-3863200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr11:3862800-3863200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
29	chr11:3862800-3863200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr11:3862800-3863200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr11:3862800-3863200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
32	chr11:3862800-3863200	Flanking Active TSS	Placenta Amnion	Placenta Amnion
33	chr11:3862800-3863400	Flanking Active TSS	Primary B cells from cord blood	blood
34	chr11:3862800-3863400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
35	chr11:3862800-3863400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
36	chr11:3862800-3863400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr11:3862800-3863400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr11:3862800-3863400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr11:3862800-3863600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
40	chr11:3862800-3863600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr11:3862800-3863600	Flanking Active TSS	Dnd41	blood
42	chr11:3863000-3863200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr11:3863000-3863200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr11:3863000-3863200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
45	chr11:3863000-3863200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr11:3863000-3863200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr11:3863000-3863200	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr11:3863000-3863200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
49	chr11:3863000-3863200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
50	chr11:3863000-3863200	Flanking Active TSS	Primary hematopoietic stem cells	blood

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