Variant report

Variant	rs55856492
Chromosome Location	chr19:41115614-41115615
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	POLR2A	chr19:41115557-41116121	HUVEC	blood vessel:	n/a	n/a
2	ELF1	chr19:41115396-41116040	K562	blood:	n/a	n/a
3	POLR2A	chr19:41115425-41116154	MCF-7	breast:	n/a	n/a
4	POLR2A	chr19:41114826-41117365	Hela-S3	cervix:	n/a	n/a
5	EGR1	chr19:41115503-41116110	MCF-7	breast:	n/a	chr19:41115854-41115865 chr19:41115592-41115602 chr19:41115852-41115866 chr19:41116023-41116033 chr19:41115854-41115864 chr19:41115579-41115589 chr19:41116023-41116036 chr19:41115850-41115864
6	POLR2A	chr19:41115435-41116123	MCF-7	breast:	n/a	n/a
7	POLR2A	chr19:41115338-41116634	HCT-116	colon:	n/a	n/a
8	CHD2	chr19:41115511-41115756	H1-hESC	embryonic stem cell:	n/a	n/a
9	TEAD4	chr19:41115569-41115987	K562	blood:	n/a	n/a
10	ZBTB7A	chr19:41115262-41115993	ECC-1	luminal epithelium:	n/a	n/a
11	POLR2A	chr19:41114946-41117153	MCF10A-Er-Src	breast:	n/a	n/a
12	EGR1	chr19:41115556-41116212	K562	blood:	n/a	chr19:41115854-41115865 chr19:41115592-41115602 chr19:41115852-41115866 chr19:41116023-41116033 chr19:41115854-41115864 chr19:41115579-41115589 chr19:41116023-41116036 chr19:41115850-41115864
13	MXI1	chr19:41115467-41116027	GM12878	blood:	n/a	n/a
14	MAX	chr19:41115347-41116128	ECC-1	luminal epithelium:	n/a	chr19:41116027-41116036
15	EGR1	chr19:41115531-41116114	ECC-1	luminal epithelium:	n/a	chr19:41115854-41115865 chr19:41115592-41115602 chr19:41115852-41115866 chr19:41116023-41116033 chr19:41115854-41115864 chr19:41115579-41115589 chr19:41116023-41116036 chr19:41115850-41115864
16	POLR2A	chr19:41115218-41116120	K562	blood:	n/a	n/a
17	MTA3	chr19:41115180-41115874	GM12878	blood:	n/a	n/a
18	MAX	chr19:41115489-41116582	Hela-S3	cervix:	n/a	chr19:41116027-41116036
19	POLR2A	chr19:41115265-41116239	Raji	blood:	n/a	n/a
20	POLR2A	chr19:41115432-41116093	GM12878	blood:	n/a	n/a
21	GABPA	chr19:41115244-41116084	MCF-7	breast:	n/a	n/a
22	POLR2A	chr19:41115432-41115704	H1-neurons	neurons:	n/a	n/a
23	MAX	chr19:41115410-41116104	ECC-1	luminal epithelium:	n/a	chr19:41116027-41116036
24	EGR1	chr19:41115567-41116198	K562	blood:	n/a	chr19:41115854-41115865 chr19:41115592-41115602 chr19:41115852-41115866 chr19:41116023-41116033 chr19:41115854-41115864 chr19:41115579-41115589 chr19:41116023-41116036 chr19:41115850-41115864
25	POLR2A	chr19:41115275-41116614	Hela-S3	cervix:	n/a	n/a
26	ZEB1	chr19:41115332-41115848	GM12878	blood:	n/a	n/a
27	ELK1	chr19:41115438-41115625	GM12878	blood:	n/a	n/a
28	POLR2A	chr19:41115443-41115954	GM12878	blood:	n/a	n/a
29	POLR2A	chr19:41115599-41116554	HUVEC	blood vessel:	n/a	n/a
30	YY1	chr19:41115458-41116156	K562	blood:	n/a	n/a
31	ELK1	chr19:41115491-41115691	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr19:41115382-41116177	GM19099	blood:	n/a	n/a
33	EGR1	chr19:41115448-41116384	HCT-116	colon:	n/a	chr19:41115854-41115865 chr19:41115592-41115602 chr19:41115852-41115866 chr19:41116023-41116033 chr19:41115854-41115864 chr19:41115579-41115589 chr19:41116023-41116036 chr19:41115850-41115864
34	POLR2A	chr19:41115380-41116060	A549	lung:	n/a	n/a
35	POLR2A	chr19:41114805-41117539	K562	blood:	n/a	n/a
36	ELF1	chr19:41115379-41115982	K562	blood:	n/a	n/a
37	TCF12	chr19:41115337-41115946	ECC-1	luminal epithelium:	n/a	n/a
38	CHD2	chr19:41115547-41115925	K562	blood:	n/a	n/a
39	POLR2A	chr19:41115383-41115725	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr19:41115503-41116070	MCF-7	breast:	n/a	n/a
41	POLR2A	chr19:41115207-41116106	PANC-1	pancreas:	n/a	n/a
42	GABPA	chr19:41115350-41115945	K562	blood:	n/a	n/a
43	CCNT2	chr19:41115533-41116102	K562	blood:	n/a	chr19:41115959-41115968
44	ZBTB7A	chr19:41115362-41116162	K562	blood:	n/a	n/a
45	MAZ	chr19:41115433-41116246	K562	blood:	n/a	chr19:41116027-41116036
46	POLR2A	chr19:41115593-41116084	GM12878	blood:	n/a	n/a
47	PAX5	chr19:41115362-41115826	GM12892	blood:	n/a	n/a
48	EBF1	chr19:41115412-41116085	GM12878	blood:	n/a	n/a
49	POLR2A	chr19:41115537-41115722	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr19:41115411-41116185	GM18951	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41115578-41115628	HEEpiC	esophagus:	n/a
2	chr19:41115578-41115628	HRPEpiC	eye:	n/a
3	chr19:41115578-41115628	A549	lung:	n/a
4	chr19:41115578-41115628	Hela-S3	cervix:	n/a
5	chr19:41115578-41115628	Caco-2	colon:	n/a
6	chr19:41115578-41115628	BE2_C	brain:	n/a
7	chr19:41115578-41115628	HAEpiC	amniotic membrane:	n/a
8	chr19:41115578-41115628	GM12878	blood:	n/a
9	chr19:41115578-41115628	HL-60	blood:	n/a
10	chr19:41115578-41115628	ECC-1	luminal epithelium:	n/a
11	chr19:41115578-41115628	PANC-1	pancreas:	n/a
12	chr19:41115578-41115628	GM19239	blood:	n/a
13	chr19:41115578-41115628	ProgFib	skin:	n/a
14	chr19:41115578-41115628	AG09319	gingival:	n/a
15	chr19:41115578-41115628	AG04449	skin:	fetal
16	chr19:41115578-41115628	RPTEC	kidney:	n/a
17	chr19:41115578-41115628	NHDF-neo	bronchial:	n/a
18	chr19:41115578-41115628	U87	brain:	n/a
19	chr19:41115578-41115628	GM12891	blood:	n/a
20	chr19:41115578-41115628	NB4	blood:	n/a
21	chr19:41115578-41115628	SKMC	muscle:	n/a
22	chr19:41115578-41115628	HCPEpiC	choroid plexus:	n/a
23	chr19:41115578-41115628	HCM	heart:	n/a
24	chr19:41115578-41115628	HIPEpiC	eye:	n/a
25	chr19:41115578-41115628	HMEC	breast:	n/a
26	chr19:41115578-41115628	HNPCEpiC	eye:	n/a
27	chr19:41115578-41115628	HEK293	kidney:	embryo
28	chr19:41115578-41115628	MCF10A-Er-Src	breast:	n/a
29	chr19:41115578-41115628	K562	blood:	n/a
30	chr19:41115578-41115628	ovcar-3	ovarian:	n/a
31	chr19:41115578-41115628	HepG2	liver:	n/a
32	chr19:41115578-41115628	LNCaP	prostate:	n/a
33	chr19:41115578-41115628	NT2-D1	testis:	n/a
34	chr19:41115578-41115628	GM12892	blood:	n/a
35	chr19:41115578-41115628	SAEC	small airway:	n/a
36	chr19:41115578-41115628	AG09309	skin:	n/a
37	chr19:41115578-41115628	SK-N-SH_RA	brain:	n/a
38	chr19:41115578-41115628	PrEC	prostate:	n/a
39	chr19:41115578-41115628	HRE	kidney:	n/a
40	chr19:41115578-41115628	SK-N-SH	brain:	n/a
41	chr19:41115578-41115628	MCF-7	breast:	n/a
42	chr19:41115578-41115628	GM06990	blood:	n/a
43	chr19:41115578-41115628	H1-hESC	embryonic stem cell:	embryo
44	chr19:41115578-41115628	T-47D	breast:	n/a
45	chr19:41115578-41115628	AG04450	lung:	fetal
46	chr19:41115578-41115628	Jurkat	blood:	n/a
47	chr19:41115578-41115628	PFSK-1	brain:	n/a
48	chr19:41115578-41115628	HUVEC	blood vessel:	n/a
49	chr19:41115578-41115628	HCT-116	colon:	n/a
50	chr19:41115578-41115628	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:150551438..150552234-chr19:41115368..41116088,2	Hela-S3	cervix:
2	chr12:7261184..7261899-chr19:41115265..41116165,2	Hela-S3	cervix:
3	chr19:40947602..40950295-chr19:41114097..41116019,2	MCF-7	breast:
4	chr19:41093158..41095920-chr19:41115359..41117293,2	K562	blood:
5	chr19:41082563..41084216-chr19:41114074..41116543,2	K562	blood:
6	chr19:40929828..40933213-chr19:41114237..41116915,3	MCF-7	breast:
7	chr19:40949481..40951384-chr19:41114617..41116181,2	MCF-7	breast:
8	chr15:73075553..73076361-chr19:41115491..41116301,2	Hela-S3	cervix:
9	chr19:41114462..41116761-chr19:41130129..41133109,2	MCF-7	breast:
10	chr19:41104685..41106959-chr19:41114610..41116415,2	MCF-7	breast:
11	chr19:41081088..41083004-chr19:41115582..41117218,2	MCF-7	breast:
12	chr19:41113914..41116044-chr19:41221538..41224427,3	MCF-7	breast:

Variant related genes	Relation type
LTBP4	TF binding region
RN7SL758P	TF binding region
LTBP4	CpG island
RN7SL758P	CpG island
ENSG00000086544	Chromatin interaction
ENSG00000159322	Chromatin interaction
ENSG00000197019	Chromatin interaction
ENSG00000268366	Chromatin interaction
ENSG00000143384	Chromatin interaction
ENSG00000160410	Chromatin interaction
ENSG00000090006	Chromatin interaction
ENSG00000139178	Chromatin interaction
ENSG00000167565	Chromatin interaction
ENSG00000123815	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11665867	1.00[ASN][1000 genomes]
rs11666504	1.00[ASN][1000 genomes]
rs11667119	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11668042	1.00[ASN][1000 genomes]
rs11672227	1.00[ASN][1000 genomes]
rs11672651	1.00[ASN][1000 genomes]
rs2077407	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36012476	1.00[ASN][1000 genomes]
rs4435368	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4624303	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55652103	1.00[ASN][1000 genomes]
rs55658896	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55723406	1.00[ASN][1000 genomes]
rs56140728	1.00[ASN][1000 genomes]
rs7253575	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7258772	1.00[ASN][1000 genomes]
rs73035918	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73047051	1.00[ASN][1000 genomes]
rs73047068	1.00[ASN][1000 genomes]
rs73047073	1.00[ASN][1000 genomes]
rs73047085	1.00[ASN][1000 genomes]
rs73047100	1.00[ASN][1000 genomes]
rs73048915	1.00[ASN][1000 genomes]
rs73051885	0.89[AMR][1000 genomes]
rs8106578	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]

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	esv1830682	chr19:40880127-41270055	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer 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	139 gene(s)	inside rSNPs	diseases
2	nsv911714	chr19:41006426-41165252	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv911715	chr19:41014922-41141434	Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
4	nsv1057634	chr19:41019512-41174259	Enhancers Active TSS Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv911717	chr19:41023511-41141434	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
6	nsv911719	chr19:41033109-41147087	Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
7	nsv911720	chr19:41033109-41156940	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
8	nsv911721	chr19:41040334-41124931	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
9	nsv911722	chr19:41040334-41176403	Bivalent Enhancer Enhancers Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
10	nsv911723	chr19:41075990-41195279	Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
11	nsv869561	chr19:41077513-41139834	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
12	nsv1064699	chr19:41086506-41174259	Genic enhancers Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
13	nsv911724	chr19:41089505-41165252	Bivalent/Poised TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
14	nsv911726	chr19:41090190-41141434	Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
15	nsv911727	chr19:41111069-41200511	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
16	nsv911728	chr19:41111069-41211056	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Strong transcription 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	38 gene(s)	inside rSNPs	diseases
17	nsv870022	chr19:41113071-41178982	Strong transcription Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41106000-41136800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr19:41109800-41122600	Weak transcription	Aorta	Aorta
3	chr19:41110000-41118200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr19:41112000-41116000	Enhancers	Stomach Mucosa	stomach
5	chr19:41112000-41116200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr19:41112000-41116200	Weak transcription	NHLF	lung
7	chr19:41114400-41116200	Weak transcription	HSMMtube	muscle
8	chr19:41114400-41119400	Weak transcription	Ovary	ovary
9	chr19:41114800-41115800	Flanking Active TSS	Primary T cells from cord blood	blood
10	chr19:41114800-41117400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
11	chr19:41115000-41116400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
12	chr19:41115000-41116400	Flanking Active TSS	K562	blood
13	chr19:41115000-41116800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr19:41115000-41118000	Weak transcription	Fetal Kidney	kidney
15	chr19:41115200-41115800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr19:41115200-41116000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr19:41115200-41116000	Flanking Active TSS	Primary hematopoietic stem cells	blood
18	chr19:41115200-41116000	Bivalent Enhancer	Brain Germinal Matrix	brain
19	chr19:41115200-41116000	Active TSS	Brain Hippocampus Middle	brain
20	chr19:41115200-41116000	Flanking Active TSS	Fetal Intestine Large	intestine
21	chr19:41115200-41116000	Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr19:41115200-41116000	Active TSS	A549	lung
23	chr19:41115200-41116000	Active TSS	Osteobl	bone
24	chr19:41115200-41116200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
25	chr19:41115200-41116200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
26	chr19:41115200-41116200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr19:41115200-41116200	Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr19:41115200-41116200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr19:41115200-41116200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr19:41115200-41116200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr19:41115200-41116200	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
32	chr19:41115200-41116400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
33	chr19:41115200-41116400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr19:41115200-41116400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
35	chr19:41115200-41116400	Flanking Bivalent TSS/Enh	Thymus	Thymus
36	chr19:41115200-41116400	Flanking Active TSS	GM12878-XiMat	blood
37	chr19:41115200-41116600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
38	chr19:41115200-41116600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
39	chr19:41115200-41116600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
40	chr19:41115200-41116600	Flanking Active TSS	Primary B cells from peripheral blood	blood
41	chr19:41115200-41116600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
42	chr19:41115200-41116600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
43	chr19:41115200-41116600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
44	chr19:41115200-41116600	Flanking Active TSS	Adipose Nuclei	Adipose
45	chr19:41115200-41116600	Flanking Bivalent TSS/Enh	HepG2	liver
46	chr19:41115200-41116800	Active TSS	Rectal Smooth Muscle	rectum
47	chr19:41115200-41117000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
48	chr19:41115200-41117400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
49	chr19:41115200-41117800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
50	chr19:41115200-41118000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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