Variant report

Variant	rs71579884
Chromosome Location	chr11:64490699-64490700
allele	C/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	SP2	chr11:64490572-64490913	K562	blood:	n/a	chr11:64490729-64490752
2	RAD21	chr11:64490612-64491458	HCT-116	colon:	n/a	chr11:64490998-64491007 chr11:64491101-64491120 chr11:64491103-64491115 chr11:64491105-64491119
3	TAF1	chr11:64490585-64490760	SK-N-SH	brain:	n/a	n/a
4	PBX3	chr11:64490474-64490969	A549	lung:	n/a	chr11:64490731-64490751
5	ZNF143	chr11:64490689-64491302	GM12878	blood:	n/a	chr11:64491215-64491233
6	MAZ	chr11:64490632-64491201	Hela-S3	cervix:	n/a	n/a
7	IRF1	chr11:64490604-64490880	K562	blood:	n/a	n/a
8	EGR1	chr11:64490558-64490751	K562	blood:	n/a	chr11:64490692-64490705
9	RCOR1	chr11:64490562-64491291	GM12878	blood:	n/a	n/a
10	CTCF	chr11:64490629-64490803	Spleen_OC	spleen:	n/a	n/a
11	TBL1XR1	chr11:64490666-64490755	K562	blood:	n/a	n/a
12	MAX	chr11:64490506-64491373	A549	lung:	n/a	n/a
13	CREB1	chr11:64490471-64491260	H1-hESC	embryonic stem cell:	n/a	n/a
14	YY1	chr11:64490580-64490750	K562	blood:	n/a	n/a
15	USF1	chr11:64490591-64490775	SK-N-SH_RA	brain:	n/a	chr11:64490633-64490649
16	CREB1	chr11:64490486-64491306	GM12878	blood:	n/a	n/a
17	REST	chr11:64489384-64491458	H1-neurons	neurons:	n/a	chr11:64491102-64491115 chr11:64490832-64490842 chr11:64489578-64489591 chr11:64490990-64491003 chr11:64489854-64489862 chr11:64490679-64490699
18	FOS	chr11:64490558-64490911	K562	blood:	n/a	n/a
19	SP1	chr11:64490516-64491032	A549	lung:	n/a	chr11:64490691-64490700
20	MAX	chr11:64490637-64490793	NB4	blood:	n/a	n/a
21	RAD21	chr11:64490579-64491425	HCT-116	colon:	n/a	chr11:64490998-64491007 chr11:64491101-64491120 chr11:64491103-64491115 chr11:64491105-64491119
22	NRF1	chr11:64490605-64490868	GM12878	blood:	n/a	n/a
23	IRF3	chr11:64490597-64490958	GM12878	blood:	n/a	n/a
24	MAZ	chr11:64490415-64491598	IMR90	lung:	n/a	n/a
25	ELF1	chr11:64490460-64490886	K562	blood:	n/a	chr11:64490639-64490651
26	FOXP2	chr11:64490586-64490854	PFSK-1	brain:	n/a	n/a
27	PBX3	chr11:64490607-64490837	GM12878	blood:	n/a	chr11:64490731-64490751
28	TAF1	chr11:64490428-64491271	H1-neurons	neurons:	n/a	n/a
29	EBF1	chr11:64490696-64490748	GM12878	blood:	n/a	n/a
30	MAZ	chr11:64490626-64491269	K562	blood:	n/a	n/a
31	CHD2	chr11:64490569-64491391	H1-hESC	embryonic stem cell:	n/a	chr11:64490636-64490646 chr11:64490942-64490952 chr11:64490949-64490959 chr11:64490732-64490742
32	HDAC2	chr11:64490481-64490758	K562	blood:	n/a	n/a
33	PBX3	chr11:64490453-64491011	A549	lung:	n/a	chr11:64490731-64490751
34	POLR2A	chr11:64490634-64490972	ECC-1	luminal epithelium:	n/a	n/a
35	CTCF	chr11:64490676-64491421	K562	blood:	n/a	chr11:64491104-64491120 chr11:64491122-64491131 chr11:64491105-64491118 chr11:64490999-64491007 chr11:64491098-64491119 chr11:64491105-64491118 chr11:64491103-64491121
36	RAD21	chr11:64490445-64492076	SK-N-SH	brain:	n/a	chr11:64490998-64491007 chr11:64491101-64491120 chr11:64490457-64490471 chr11:64491103-64491115 chr11:64491105-64491119
37	MAX	chr11:64490554-64491248	ECC-1	luminal epithelium:	n/a	n/a
38	YY1	chr11:64490547-64491271	K562	blood:	n/a	chr11:64491101-64491115
39	SP1	chr11:64490586-64490901	K562	blood:	n/a	chr11:64490691-64490700
40	EGR1	chr11:64490577-64490825	K562	blood:	n/a	chr11:64490692-64490705
41	GABPA	chr11:64490551-64490876	K562	blood:	n/a	n/a
42	CEBPB	chr11:64490595-64490785	Hela-S3	cervix:	n/a	n/a
43	SP1	chr11:64490599-64490931	GM12878	blood:	n/a	chr11:64490691-64490700
44	RAD21	chr11:64490585-64490754	SK-N-SH_RA	brain:	n/a	n/a
45	CHD2	chr11:64490569-64491247	K562	blood:	n/a	chr11:64490636-64490646 chr11:64490942-64490952 chr11:64490949-64490959 chr11:64490732-64490742
46	PBX3	chr11:64490579-64490993	SK-N-SH	brain:	n/a	chr11:64490731-64490751
47	E2F4	chr11:64490658-64490757	MCF10A-Er-Src	breast:	n/a	chr11:64490691-64490700
48	YY1	chr11:64490573-64490849	SK-N-SH_RA	brain:	n/a	n/a
49	SP1	chr11:64490578-64491179	GM12878	blood:	n/a	chr11:64491128-64491137 chr11:64491126-64491138 chr11:64490691-64490700 chr11:64491126-64491138
50	RCOR1	chr11:64490499-64491182	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:64490672-64490722	CMK	blood:	n/a
2	chr11:64490672-64490722	K562	blood:	n/a
3	chr11:64490672-64490722	HCPEpiC	choroid plexus:	n/a
4	chr11:64490672-64490722	HPAEpiC	pulmonary alveolar:	n/a
5	chr11:64490672-64490722	AoSMC	blood vessel:	n/a
6	chr11:64490672-64490722	HCF	heart:	n/a
7	chr11:64490672-64490722	Jurkat	blood:	n/a
8	chr11:64490672-64490722	SKMC	muscle:	n/a
9	chr11:64490672-64490722	AG10803	skin:	n/a
10	chr11:64490672-64490722	AG04450	lung:	fetal
11	chr11:64490672-64490722	ECC-1	luminal epithelium:	n/a
12	chr11:64490672-64490722	NB4	blood:	n/a
13	chr11:64490672-64490722	A549	lung:	n/a
14	chr11:64490672-64490722	Hela-S3	cervix:	n/a
15	chr11:64490672-64490722	AG09319	gingival:	n/a
16	chr11:64490672-64490722	MCF-7	breast:	n/a
17	chr11:64490672-64490722	HUVEC	blood vessel:	n/a
18	chr11:64490672-64490722	T-47D	breast:	n/a
19	chr11:64490672-64490722	HCM	heart:	n/a
20	chr11:64490672-64490722	NHBE	bronchial:	n/a
21	chr11:64490672-64490722	HEEpiC	esophagus:	n/a
22	chr11:64490672-64490722	U87	brain:	n/a
23	chr11:64490672-64490722	HEK293	kidney:	embryo
24	chr11:64490672-64490722	GM12892	blood:	n/a
25	chr11:64490672-64490722	ovcar-3	ovarian:	n/a
26	chr11:64490672-64490722	NHDF-neo	bronchial:	n/a
27	chr11:64490672-64490722	HRE	kidney:	n/a
28	chr11:64490672-64490722	HMEC	breast:	n/a
29	chr11:64490672-64490722	AG04449	skin:	fetal
30	chr11:64490672-64490722	ProgFib	skin:	n/a
31	chr11:64490672-64490722	GM19239	blood:	n/a
32	chr11:64490672-64490722	IMR90	lung:	fetal
33	chr11:64490672-64490722	PANC-1	pancreas:	n/a
34	chr11:64490672-64490722	HNPCEpiC	eye:	n/a
35	chr11:64490672-64490722	PFSK-1	brain:	n/a
36	chr11:64490672-64490722	AG09309	skin:	n/a
37	chr11:64490672-64490722	RPTEC	kidney:	n/a
38	chr11:64490672-64490722	HCT-116	colon:	n/a
39	chr11:64490672-64490722	HL-60	blood:	n/a
40	chr11:64490672-64490722	NT2-D1	testis:	n/a
41	chr11:64490672-64490722	SAEC	small airway:	n/a
42	chr11:64490672-64490722	GM12878	blood:	n/a
43	chr11:64490672-64490722	HAEpiC	amniotic membrane:	n/a
44	chr11:64490672-64490722	NH-A	brain:	n/a
45	chr11:64490672-64490722	MCF10A-Er-Src	breast:	n/a
46	chr11:64490672-64490722	SK-N-MC	brain:	n/a
47	chr11:64490672-64490722	BE2_C	brain:	n/a
48	chr11:64490672-64490722	GM06990	blood:	n/a
49	chr11:64490672-64490722	LNCaP	prostate:	n/a
50	chr11:64490672-64490722	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:64489616..64492284-chr11:64509871..64511516,3	K562	blood:
2	chr11:64490193..64492198-chr11:64544563..64546459,2	MCF-7	breast:
3	chr11:64489296..64491902-chr11:64644473..64646300,2	MCF-7	breast:
4	chr11:64488142..64490863-chr11:64506214..64508875,2	MCF-7	breast:
5	chr11:64490496..64491176-chr11:64510209..64510932,2	MCF-7	breast:
6	chr11:64478255..64481463-chr11:64489766..64492365,3	K562	blood:
7	chr11:64490664..64492722-chr11:64991494..64993936,2	MCF-7	breast:
8	chr11:64420274..64420985-chr11:64490663..64491460,2	K562	blood:
9	chr11:64489351..64492621-chr11:64507509..64512935,5	K562	blood:

Variant related genes	Relation type
NRXN2	TF binding region
NRXN2	CpG island
ENSG00000168066	Chromatin interaction
ENSG00000110047	Chromatin interaction
ENSG00000068831	Chromatin interaction
ENSG00000269038	Chromatin interaction
ENSG00000110076	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv468596	chr11:64334114-64527080	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv555195	chr11:64334114-64527080	Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv897694	chr11:64334114-64584959	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
4	nsv818842	chr11:64345448-64546391	Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
5	nsv528506	chr11:64345448-64701030	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
6	nsv555196	chr11:64357072-64559898	Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
7	nsv897695	chr11:64357072-64701030	Weak transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
8	nsv1051350	chr11:64372906-64533632	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv555198	chr11:64373899-64573589	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
10	esv1804443	chr11:64386453-64534785	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
11	nsv897697	chr11:64447420-64584959	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
12	nsv897698	chr11:64447420-64621573	Active TSS Bivalent Enhancer Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
13	nsv897699	chr11:64447420-64638041	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
14	nsv897700	chr11:64447420-64701030	Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription 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	1071 gene(s)	inside rSNPs	diseases
15	nsv359	chr11:64477008-64502873	Bivalent/Poised TSS Flanking Active TSS Genic enhancers Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
16	nsv555202	chr11:64477050-64573589	Strong transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
17	nsv468597	chr11:64477050-64584959	Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
18	nsv468598	chr11:64477050-64584959	Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
19	nsv555203	chr11:64477050-64584959	Strong transcription Genic enhancers Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
20	nsv1049744	chr11:64486615-64630149	Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
21	nsv832189	chr11:64487183-64620199	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
22	esv3324432	chr11:64489201-64492249	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
23	esv3409975	chr11:64489426-64491724	Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64488600-64491200	Active TSS	Brain Angular Gyrus	brain
2	chr11:64488600-64491200	Active TSS	Brain Inferior Temporal Lobe	brain
3	chr11:64489000-64491200	Active TSS	Brain Anterior Caudate	brain
4	chr11:64489400-64491000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
5	chr11:64489400-64491200	Active TSS	Brain Hippocampus Middle	brain
6	chr11:64489600-64491200	Active TSS	Fetal Brain Female	brain
7	chr11:64489800-64490800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
8	chr11:64490000-64491400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
9	chr11:64490200-64490800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:64490200-64490800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr11:64490200-64490800	Active TSS	Cortex derived primary cultured neurospheres	brain
12	chr11:64490200-64491000	Weak transcription	Fetal Brain Male	brain
13	chr11:64490200-64491200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr11:64490200-64491200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr11:64490200-64491200	Active TSS	Brain Cingulate Gyrus	brain
16	chr11:64490200-64491200	Active TSS	Brain Substantia Nigra	brain
17	chr11:64490200-64491400	Active TSS	iPS-15b Cell Line	embryonic stem cell
18	chr11:64490400-64491000	Active TSS	Primary T helper cells PMA-I stimulated	--
19	chr11:64490400-64491000	Active TSS	Brain Germinal Matrix	brain
20	chr11:64490400-64491200	Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr11:64490400-64491200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr11:64490400-64491200	Active TSS	HSMM	muscle
23	chr11:64490600-64490800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr11:64490600-64490800	Active TSS	Primary B cells from cord blood	blood
25	chr11:64490600-64490800	Active TSS	Primary B cells from peripheral blood	blood
26	chr11:64490600-64490800	Active TSS	Primary T cells fromperipheralblood	blood
27	chr11:64490600-64490800	Enhancers	Primary hematopoietic stem cells	blood
28	chr11:64490600-64490800	Active TSS	Primary hematopoietic stem cells short term culture	blood
29	chr11:64490600-64490800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
30	chr11:64490600-64490800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr11:64490600-64490800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr11:64490600-64490800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr11:64490600-64490800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr11:64490600-64490800	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr11:64490600-64490800	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr11:64490600-64490800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
37	chr11:64490600-64490800	Active TSS	Adipose Nuclei	Adipose
38	chr11:64490600-64490800	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
39	chr11:64490600-64490800	Bivalent/Poised TSS	Fetal Stomach	stomach
40	chr11:64490600-64490800	Bivalent/Poised TSS	Fetal Thymus	thymus
41	chr11:64490600-64490800	Active TSS	Rectal Mucosa Donor 31	rectum
42	chr11:64490600-64490800	Active TSS	Skeletal Muscle Male	skeletal muscle
43	chr11:64490600-64490800	Active TSS	Stomach Smooth Muscle	stomach
44	chr11:64490600-64490800	Bivalent/Poised TSS	Thymus	Thymus
45	chr11:64490600-64490800	Active TSS	Dnd41	blood
46	chr11:64490600-64490800	Active TSS	HMEC	breast
47	chr11:64490600-64490800	Active TSS	Monocytes-CD14+_RO01746	blood
48	chr11:64490600-64490800	Bivalent/Poised TSS	NH-A	brain
49	chr11:64490600-64490800	Bivalent/Poised TSS	NHLF	lung
50	chr11:64490600-64491000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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