Variant report

Variant	rs73047963
Chromosome Location	chr19:41102876-41102877
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	RCOR1	chr19:41102821-41102923	K562	blood:	n/a	n/a
2	POLR2A	chr19:41102699-41103030	HCT-116	colon:	n/a	n/a
3	MYC	chr19:41102832-41102915	K562	blood:	n/a	chr19:41102890-41102897
4	NFYA	chr19:41102795-41103019	Hela-S3	cervix:	n/a	chr19:41102948-41102962 chr19:41102947-41102962 chr19:41102986-41103000 chr19:41102951-41102963 chr19:41102947-41102962
5	TBP	chr19:41102750-41103277	K562	blood:	n/a	n/a
6	RCOR1	chr19:41102726-41103160	K562	blood:	n/a	n/a
7	SP2	chr19:41102860-41103003	K562	blood:	n/a	n/a
8	POLR2A	chr19:41102585-41103550	K562	blood:	n/a	n/a
9	GATA3	chr19:41102545-41105109	A549	lung:	n/a	n/a
10	POLR2A	chr19:41102728-41103301	K562	blood:	n/a	n/a
11	MAZ	chr19:41102747-41102925	HepG2	liver:	n/a	chr19:41102890-41102897
12	HMGN3	chr19:41102812-41103390	K562	blood:	n/a	n/a
13	FOSL2	chr19:41102432-41103856	A549	lung:	n/a	chr19:41102949-41102958 chr19:41102987-41102996
14	MAX	chr19:41102746-41102884	HepG2	liver:	n/a	n/a
15	E2F6	chr19:41102557-41103412	A549	lung:	n/a	chr19:41102989-41102998 chr19:41102990-41103002 chr19:41102951-41102960 chr19:41102975-41102985
16	MAX	chr19:41102846-41103046	Hela-S3	cervix:	n/a	chr19:41102890-41102897
17	POLR2A	chr19:41102555-41103598	PFSK-1	brain:	n/a	n/a
18	NFYB	chr19:41102796-41103064	Hela-S3	cervix:	n/a	chr19:41102949-41102964 chr19:41102948-41102962 chr19:41102947-41102962 chr19:41102986-41103000 chr19:41102987-41103002 chr19:41102951-41102963 chr19:41102947-41102962
19	CHD2	chr19:41102750-41102972	K562	blood:	n/a	n/a
20	POLR2A	chr19:41102760-41103440	PFSK-1	brain:	n/a	n/a
21	E2F4	chr19:41102823-41103058	MCF10A-Er-Src	breast:	n/a	chr19:41102989-41102998 chr19:41102990-41103002 chr19:41102992-41103003 chr19:41102951-41102960 chr19:41102975-41102985
22	MAX	chr19:41102693-41103294	A549	lung:	n/a	chr19:41102890-41102897
23	MAX	chr19:41102602-41103236	HepG2	liver:	n/a	chr19:41102890-41102897
24	CTCF	chr19:41102201-41106331	A549	lung:	n/a	chr19:41104670-41104688 chr19:41104671-41104687 chr19:41102391-41102404 chr19:41104665-41104686
25	TCF12	chr19:41102578-41103013	A549	lung:	n/a	n/a
26	PBX3	chr19:41102783-41103230	SK-N-SH	brain:	n/a	chr19:41102950-41102959
27	E2F6	chr19:41102607-41103352	K562	blood:	n/a	chr19:41102989-41102998 chr19:41102990-41103002 chr19:41102951-41102960 chr19:41102975-41102985
28	MAX	chr19:41102662-41103235	K562	blood:	n/a	chr19:41102890-41102897
29	MAX	chr19:41102508-41103511	HCT-116	colon:	n/a	chr19:41102890-41102897
30	MAX	chr19:41102634-41103407	MCF-7	breast:	n/a	chr19:41102890-41102897
31	NFYB	chr19:41102828-41103028	GM12878	blood:	n/a	chr19:41102949-41102964 chr19:41102948-41102962 chr19:41102947-41102962 chr19:41102986-41103000 chr19:41102987-41103002 chr19:41102951-41102963 chr19:41102947-41102962
32	PBX3	chr19:41102702-41103310	SK-N-SH	brain:	n/a	chr19:41102950-41102959
33	CHD2	chr19:41102841-41103057	Hela-S3	cervix:	n/a	n/a
34	MAX	chr19:41102513-41103404	ECC-1	luminal epithelium:	n/a	chr19:41102890-41102897
35	PBX3	chr19:41102542-41103274	A549	lung:	n/a	chr19:41102950-41102959
36	EGR1	chr19:41102822-41103278	K562	blood:	n/a	n/a
37	CCNT2	chr19:41102831-41103315	K562	blood:	n/a	n/a
38	NFYA	chr19:41102632-41103106	K562	blood:	n/a	chr19:41102948-41102962 chr19:41102947-41102962 chr19:41102986-41103000 chr19:41102951-41102963 chr19:41102947-41102962
39	ZBTB7A	chr19:41102629-41103055	ECC-1	luminal epithelium:	n/a	n/a
40	ZNF263	chr19:41102435-41102892	HEK293-T-REx	kidney:	n/a	n/a
41	SIX5	chr19:41102535-41105874	A549	lung:	n/a	n/a
42	HCFC1	chr19:41102810-41103007	K562	blood:	n/a	n/a
43	SP1	chr19:41102545-41103246	A549	lung:	n/a	chr19:41102940-41102961 chr19:41102978-41102999 chr19:41102775-41102789 chr19:41102775-41102784
44	MAX	chr19:41102715-41103277	K562	blood:	n/a	chr19:41102890-41102897
45	E2F6	chr19:41102367-41104923	A549	lung:	n/a	chr19:41102989-41102998 chr19:41102990-41103002 chr19:41104309-41104323 chr19:41102951-41102960 chr19:41102975-41102985 chr19:41104665-41104682
46	E2F6	chr19:41102596-41103392	H1-hESC	embryonic stem cell:	n/a	chr19:41102989-41102998 chr19:41102990-41103002 chr19:41102951-41102960 chr19:41102975-41102985
47	ELF1	chr19:41102821-41103026	K562	blood:	n/a	n/a
48	E2F6	chr19:41102701-41103290	K562	blood:	n/a	chr19:41102989-41102998 chr19:41102990-41103002 chr19:41102951-41102960 chr19:41102975-41102985
49	MYC	chr19:41102715-41103174	K562	blood:	n/a	chr19:41102890-41102897
50	TBL1XR1	chr19:41102692-41102928	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41102858-41102908	HL-60	blood:	n/a
2	chr19:41102858-41102908	RPTEC	kidney:	n/a
3	chr19:41102858-41102908	GM12878	blood:	n/a
4	chr19:41102858-41102908	H1-hESC	embryonic stem cell:	embryo
5	chr19:41102858-41102908	NB4	blood:	n/a
6	chr19:41102858-41102908	HCF	heart:	n/a
7	chr19:41102858-41102908	K562	blood:	n/a
8	chr19:41102858-41102908	T-47D	breast:	n/a
9	chr19:41102858-41102908	AoSMC	blood vessel:	n/a
10	chr19:41102858-41102908	NHDF-neo	bronchial:	n/a
11	chr19:41102858-41102908	HIPEpiC	eye:	n/a
12	chr19:41102858-41102908	U87	brain:	n/a
13	chr19:41102858-41102908	HEEpiC	esophagus:	n/a
14	chr19:41102858-41102908	SK-N-MC	brain:	n/a
15	chr19:41102858-41102908	ProgFib	skin:	n/a
16	chr19:41102858-41102908	NH-A	brain:	n/a
17	chr19:41102858-41102908	Jurkat	blood:	n/a
18	chr19:41102858-41102908	HCPEpiC	choroid plexus:	n/a
19	chr19:41102858-41102908	PANC-1	pancreas:	n/a
20	chr19:41102858-41102908	MCF10A-Er-Src	breast:	n/a
21	chr19:41102858-41102908	AG04449	skin:	fetal
22	chr19:41102858-41102908	HEK293	kidney:	embryo
23	chr19:41102858-41102908	AG09319	gingival:	n/a
24	chr19:41102858-41102908	HCM	heart:	n/a
25	chr19:41102858-41102908	HPAEpiC	pulmonary alveolar:	n/a
26	chr19:41102858-41102908	HRCEpiC	kidney:	n/a
27	chr19:41102858-41102908	HCT-116	colon:	n/a
28	chr19:41102858-41102908	BJ	skin:	n/a
29	chr19:41102858-41102908	BE2_C	brain:	n/a
30	chr19:41102858-41102908	CMK	blood:	n/a
31	chr19:41102858-41102908	PFSK-1	brain:	n/a
32	chr19:41102858-41102908	NT2-D1	testis:	n/a
33	chr19:41102858-41102908	HAEpiC	amniotic membrane:	n/a
34	chr19:41102858-41102908	ovcar-3	ovarian:	n/a
35	chr19:41102858-41102908	HNPCEpiC	eye:	n/a
36	chr19:41102858-41102908	AG04450	lung:	fetal
37	chr19:41102858-41102908	GM12891	blood:	n/a
38	chr19:41102858-41102908	SAEC	small airway:	n/a
39	chr19:41102858-41102908	NHBE	bronchial:	n/a
40	chr19:41102858-41102908	AG09309	skin:	n/a
41	chr19:41102858-41102908	LNCaP	prostate:	n/a
42	chr19:41102858-41102908	A549	lung:	n/a
43	chr19:41102858-41102908	GM06990	blood:	n/a
44	chr19:41102858-41102908	Hepatocyte	liver:	n/a
45	chr19:41102858-41102908	ECC-1	luminal epithelium:	n/a
46	chr19:41102858-41102908	SKMC	muscle:	n/a
47	chr19:41102858-41102908	MCF-7	breast:	n/a
48	chr19:41102858-41102908	HepG2	liver:	n/a
49	chr19:41102858-41102908	IMR90	lung:	fetal
50	chr19:41102858-41102908	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:41074575..41077063-chr19:41102661..41104617,3	MCF-7	breast:
2	chr19:40967363..40973578-chr19:41101518..41109514,8	K562	blood:
3	chr19:40948223..40951399-chr19:41100513..41104736,3	MCF-7	breast:
4	chr19:41074953..41077910-chr19:41101103..41104097,3	MCF-7	breast:
5	chr19:41081761..41084466-chr19:41100896..41105533,6	MCF-7	breast:
6	chr19:41093850..41097927-chr19:41099715..41103880,5	K562	blood:
7	chr19:41094390..41097237-chr19:41101497..41103880,2	K562	blood:
8	chr19:41075233..41077864-chr19:41102311..41105229,3	K562	blood:
9	chr19:41031800..41040224-chr19:41101608..41111828,17	K562	blood:
10	chr19:41081136..41084687-chr19:41102465..41104575,4	K562	blood:
11	chr19:41101978..41104325-chr19:41119218..41120800,2	MCF-7	breast:
12	chr12:54674360..54676219-chr19:41102639..41105279,2	K562	blood:
13	chr19:41036449..41038732-chr19:41102668..41104519,2	K562	blood:
14	chr19:41082667..41084687-chr19:41102465..41104415,2	K562	blood:
15	chr19:41075285..41077468-chr19:41102388..41105229,2	K562	blood:

Variant related genes	Relation type
LTBP4	TF binding region
LTBP4	CpG island
ENSG00000160460	Chromatin interaction
ENSG00000135486	Chromatin interaction
ENSG00000160410	Chromatin interaction
ENSG00000167565	Chromatin interaction
ENSG00000268366	Chromatin interaction
ENSG00000090013	Chromatin interaction
ENSG00000090006	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11083560	0.93[ASN][1000 genomes]
rs2246761	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2303728	0.90[ASN][1000 genomes]
rs3786527	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4802079	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55740667	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55815263	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62107907	0.98[ASN][1000 genomes]
rs62107911	0.87[ASN][1000 genomes]
rs62107913	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73047967	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]

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	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	nsv911716	chr19:41023511-41109456	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	nsv911725	chr19:41090190-41114065	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS 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	25 gene(s)	inside rSNPs	diseases
16	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41095200-41103200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr19:41101200-41103200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr19:41101200-41104200	Weak transcription	Dnd41	blood
4	chr19:41102200-41103000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:41102200-41106400	Bivalent Enhancer	Placenta	Placenta
6	chr19:41102400-41103200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
7	chr19:41102400-41103200	Bivalent Enhancer	Colon Smooth Muscle	Colon
8	chr19:41102400-41103200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
9	chr19:41102400-41104800	Bivalent Enhancer	Fetal Brain Male	brain
10	chr19:41102400-41108600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
11	chr19:41102400-41109200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
12	chr19:41102600-41103000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr19:41102600-41103000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
14	chr19:41102600-41103000	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr19:41102600-41103000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
16	chr19:41102600-41103000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr19:41102600-41103000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
18	chr19:41102600-41103000	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
19	chr19:41102600-41103000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr19:41102600-41103000	Flanking Active TSS	Hela-S3	cervix
21	chr19:41102600-41103000	Bivalent/Poised TSS	HSMMtube	muscle
22	chr19:41102600-41103000	Flanking Active TSS	HUVEC	blood vessel
23	chr19:41102600-41103000	Flanking Active TSS	K562	blood
24	chr19:41102600-41103200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
25	chr19:41102600-41103200	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
26	chr19:41102600-41103200	Bivalent Enhancer	Brain Anterior Caudate	brain
27	chr19:41102600-41103200	Bivalent Enhancer	Brain Cingulate Gyrus	brain
28	chr19:41102600-41103200	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr19:41102600-41103200	Bivalent Enhancer	Fetal Intestine Large	intestine
30	chr19:41102600-41103200	Bivalent Enhancer	Fetal Thymus	thymus
31	chr19:41102600-41103200	Bivalent/Poised TSS	Psoas Muscle	Psoas
32	chr19:41102600-41103200	Bivalent Enhancer	Small Intestine	intestine
33	chr19:41102600-41103200	Enhancers	NHLF	lung
34	chr19:41102600-41103600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr19:41102600-41103600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
36	chr19:41102600-41103600	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr19:41102600-41103600	Enhancers	Lung	lung
38	chr19:41102600-41103600	Bivalent Enhancer	Stomach Mucosa	stomach
39	chr19:41102600-41103800	Bivalent Enhancer	Fetal Lung	lung
40	chr19:41102600-41104200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr19:41102600-41104200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
42	chr19:41102600-41104600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr19:41102600-41104800	Bivalent Enhancer	Fetal Heart	heart
44	chr19:41102600-41105000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
45	chr19:41102600-41105600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
46	chr19:41102600-41108200	Bivalent Enhancer	Primary B cells from cord blood	blood
47	chr19:41102600-41108200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
48	chr19:41102800-41103000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
49	chr19:41102800-41103000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr19:41102800-41103000	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood

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