Variant report

Variant	esv1818841
Chromosome Location	chr19:35848339-35863299
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:195)
CpG islands
(count:366)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:195 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:35849261-35849449	K562	blood:	n/a	n/a
2	BACH1	chr19:35851866-35852079	K562	blood:	n/a	n/a
3	CEBPB	chr19:35849029-35849356	A549	lung:	n/a	chr19:35849192-35849203
4	CEBPB	chr19:35849025-35849368	K562	blood:	n/a	chr19:35849192-35849203
5	CEBPB	chr19:35861266-35861524	A549	lung:	n/a	chr19:35861400-35861411
6	CEBPB	chr19:35861320-35861547	K562	blood:	n/a	chr19:35861400-35861411
7	CEBPB	chr19:35849083-35849292	H1-hESC	embryonic stem cell:	n/a	chr19:35849192-35849203
8	CEBPB	chr19:35849037-35849249	K562	blood:	n/a	chr19:35849192-35849203
9	CEBPB	chr19:35849039-35849353	Hela-S3	cervix:	n/a	chr19:35849192-35849203
10	CEBPB	chr19:35849027-35849357	HepG2	liver:	n/a	chr19:35849192-35849203
11	CEBPB	chr19:35861294-35861521	HepG2	liver:	n/a	chr19:35861400-35861411
12	CEBPB	chr19:35861291-35861545	IMR90	lung:	n/a	chr19:35861400-35861411
13	CEBPB	chr19:35849017-35849385	IMR90	lung:	n/a	chr19:35849192-35849203
14	CTCF	chr19:35849856-35850054	Gliobla	brain:	n/a	n/a
15	CTCF	chr19:35862325-35862487	K562	blood:	n/a	n/a
16	CTCF	chr19:35862115-35862183	GM13976	blood:	n/a	n/a
17	CTCF	chr19:35862357-35862469	NHEK	skin:	n/a	n/a
18	CTCF	chr19:35849907-35849974	MCF-7	breast:	n/a	n/a
19	CTCF	chr19:35862244-35862528	K562	blood:	n/a	n/a
20	CTCF	chr19:35849780-35849930	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr19:35849820-35849970	GM12866	blood:	n/a	n/a
22	CTCF	chr19:35849891-35850044	NHEK	skin:	n/a	n/a
23	CTCF	chr19:35862239-35862573	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr19:35849870-35850050	GM12878	blood:	n/a	n/a
25	CTCF	chr19:35862400-35862454	GM20000	blood:	n/a	n/a
26	CTCF	chr19:35849817-35850032	GM20000	blood:	n/a	n/a
27	CTCF	chr19:35849792-35850103	GM19239	blood:	n/a	n/a
28	CTCF	chr19:35848640-35848790	BE2_C	brain:	n/a	n/a
29	CTCF	chr19:35849840-35849990	GM12866	blood:	n/a	n/a
30	CTCF	chr19:35848542-35848564	GM13976	blood:	n/a	n/a
31	CTCF	chr19:35862336-35862493	MCF-7	breast:	n/a	n/a
32	CTCF	chr19:35862328-35862517	Fibrobl	skin:	n/a	n/a
33	CTCF	chr19:35862297-35862532	MCF-7	breast:	n/a	n/a
34	CTCF	chr19:35849858-35849961	HepG2	liver:	n/a	n/a
35	CTCF	chr19:35849780-35849930	HepG2	liver:	n/a	n/a
36	CTCF	chr19:35849940-35850021	MCF-7	breast:	n/a	n/a
37	CTCF	chr19:35862431-35862518	GM13976	blood:	n/a	n/a
38	CTCF	chr19:35862354-35862478	MCF-7	breast:	n/a	n/a
39	CTCF	chr19:35849780-35849930	HMEC	breast:	n/a	n/a
40	CTCF	chr19:35862351-35862447	HepG2	liver:	n/a	n/a
41	CTCF	chr19:35848580-35848730	HEK293	kidney:	n/a	n/a
42	CTCF	chr19:35862340-35862508	A549	lung:	n/a	n/a
43	CTCF	chr19:35849857-35850020	GM10248	blood:	n/a	n/a
44	CTCF	chr19:35849790-35850033	K562	blood:	n/a	n/a
45	CTCF	chr19:35849800-35849950	GM12867	blood:	n/a	n/a
46	CTCF	chr19:35849760-35849910	GM12874	blood:	n/a	n/a
47	CTCF	chr19:35862100-35862172	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr19:35848520-35848670	GM12868	blood:	n/a	n/a
49	CTCF	chr19:35849861-35850024	ProgFib	skin:	n/a	n/a
50	CTCF	chr19:35849840-35849990	GM06990	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:35850463-35850513	GM19239	blood:	n/a
2	chr19:35848801-35848851	SK-N-SH	brain:	n/a
3	chr19:35849024-35849074	CMK	blood:	n/a
4	chr19:35849176-35849226	BJ	skin:	n/a
5	chr19:35861862-35861912	HPAEpiC	pulmonary alveolar:	n/a
6	chr19:35849393-35849443	PrEC	prostate:	n/a
7	chr19:35849024-35849074	HCM	heart:	n/a
8	chr19:35861862-35861912	SK-N-MC	brain:	n/a
9	chr19:35848801-35848851	BE2_C	brain:	n/a
10	chr19:35861862-35861912	NHDF-neo	bronchial:	n/a
11	chr19:35850463-35850513	Hela-S3	cervix:	n/a
12	chr19:35849024-35849074	GM12878	blood:	n/a
13	chr19:35849393-35849443	NH-A	brain:	n/a
14	chr19:35849393-35849443	HCT-116	colon:	n/a
15	chr19:35849393-35849443	RPTEC	kidney:	n/a
16	chr19:35849393-35849443	A549	lung:	n/a
17	chr19:35849393-35849443	HUVEC	blood vessel:	n/a
18	chr19:35849024-35849074	HRCEpiC	kidney:	n/a
19	chr19:35848801-35848851	NHBE	bronchial:	n/a
20	chr19:35849024-35849074	Caco-2	colon:	n/a
21	chr19:35849176-35849226	RPTEC	kidney:	n/a
22	chr19:35849176-35849226	H1-hESC	embryonic stem cell:	embryo
23	chr19:35848801-35848851	NB4	blood:	n/a
24	chr19:35848801-35848851	AG09309	skin:	n/a
25	chr19:35850463-35850513	Caco-2	colon:	n/a
26	chr19:35861862-35861912	HL-60	blood:	n/a
27	chr19:35849024-35849074	HNPCEpiC	eye:	n/a
28	chr19:35861862-35861912	HAEpiC	amniotic membrane:	n/a
29	chr19:35849393-35849443	U87	brain:	n/a
30	chr19:35849024-35849074	HRPEpiC	eye:	n/a
31	chr19:35848801-35848851	SK-N-SH_RA	brain:	n/a
32	chr19:35849024-35849074	GM19239	blood:	n/a
33	chr19:35849024-35849074	ovcar-3	ovarian:	n/a
34	chr19:35861862-35861912	HEEpiC	esophagus:	n/a
35	chr19:35849024-35849074	ProgFib	skin:	n/a
36	chr19:35849176-35849226	HRCEpiC	kidney:	n/a
37	chr19:35848801-35848851	AG04449	skin:	fetal
38	chr19:35850463-35850513	RPTEC	kidney:	n/a
39	chr19:35849024-35849074	SKMC	muscle:	n/a
40	chr19:35850463-35850513	CMK	blood:	n/a
41	chr19:35849024-35849074	HMEC	breast:	n/a
42	chr19:35848801-35848851	HEK293	kidney:	embryo
43	chr19:35849393-35849443	NT2-D1	testis:	n/a
44	chr19:35849176-35849226	U87	brain:	n/a
45	chr19:35849393-35849443	AG04449	skin:	fetal
46	chr19:35850463-35850513	BJ	skin:	n/a
47	chr19:35849176-35849226	A549	lung:	n/a
48	chr19:35849393-35849443	AG10803	skin:	n/a
49	chr19:35848801-35848851	HIPEpiC	eye:	n/a
50	chr19:35850463-35850513	H1-hESC	embryonic stem cell:	embryo

(count:1 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:35847716..35849933-chr19:35855045..35856568,2	MCF-7	breast:

No data

Variant related genes	Relation type
FFAR3	TF binding region
GPR42	TF binding region
FFAR3	CpG island
GPR42	CpG island
ENSG00000185897	chromatin interactions

Extended variants
information (count: 408 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:408 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12459138	chr19:35848339-35848340	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184782236	chr19:35848349-35848350	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs199783876	chr19:35848434-35848435	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs188378673	chr19:35848464-35848465	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs531908027	chr19:35848470-35848471	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs370785484	chr19:35848484-35848485	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs180688042	chr19:35848497-35848498	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs539733534	chr19:35848525-35848526	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs74409207	chr19:35848543-35848544	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs56778651	chr19:35848555-35848556	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs146957350	chr19:35848567-35848568	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs117325178	chr19:35848581-35848582	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs144608354	chr19:35848585-35848586	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs556012300	chr19:35848590-35848591	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs551612974	chr19:35848648-35848649	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs571655164	chr19:35848681-35848682	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs572545638	chr19:35848684-35848685	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs534119242	chr19:35848705-35848706	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs148483143	chr19:35848718-35848719	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs374551699	chr19:35848801-35848802	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs564308596	chr19:35848802-35848803	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs533405847	chr19:35848830-35848831	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs60182696	chr19:35848858-35848859	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs533676772	chr19:35848866-35848867	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs12608878	chr19:35848867-35848868	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs147554474	chr19:35848883-35848884	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs142490306	chr19:35848923-35848924	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs7251096	chr19:35848955-35848956	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs113192141	chr19:35848956-35848957	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs551493036	chr19:35848969-35848970	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs140872408	chr19:35848996-35848997	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs17272288	chr19:35849061-35849062	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs367544251	chr19:35849136-35849137	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs537004693	chr19:35849143-35849144	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs537890763	chr19:35849176-35849177	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs143244108	chr19:35849183-35849184	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs58199607	chr19:35849184-35849185	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs536178273	chr19:35849273-35849274	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs146704794	chr19:35849283-35849284	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs555975639	chr19:35849306-35849307	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs572634896	chr19:35849343-35849344	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs381099	chr19:35849410-35849411	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs375854528	chr19:35849428-35849429	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs369874702	chr19:35849436-35849437	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs558280055	chr19:35849441-35849442	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs10412120	chr19:35849447-35849448	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs539350244	chr19:35849471-35849472	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs543374650	chr19:35849472-35849473	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs59198030	chr19:35849563-35849564	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs62109580	chr19:35849666-35849667	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35838200-35849200	Weak transcription	Brain Hippocampus Middle	brain
2	chr19:35839200-35848600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr19:35839200-35848800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr19:35840800-35848400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr19:35843800-35848600	Weak transcription	Gastric	stomach
6	chr19:35844000-35848400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr19:35844000-35848800	Weak transcription	Primary hematopoietic stem cells	blood
8	chr19:35844000-35849000	Weak transcription	Ovary	ovary
9	chr19:35844000-35849000	Weak transcription	Spleen	Spleen
10	chr19:35844200-35848400	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr19:35844200-35848400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr19:35844200-35848400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr19:35844200-35848800	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr19:35844200-35849000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr19:35844200-35849000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr19:35844600-35849000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr19:35845000-35848400	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr19:35846400-35848800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr19:35847000-35848400	Weak transcription	HepG2	liver
20	chr19:35847200-35848600	Weak transcription	Adipose Nuclei	Adipose
21	chr19:35847200-35848800	Weak transcription	Liver	Liver
22	chr19:35847200-35852000	Weak transcription	GM12878-XiMat	blood
23	chr19:35847600-35848600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr19:35847600-35848600	Weak transcription	Fetal Lung	lung
25	chr19:35847600-35848800	Weak transcription	Fetal Muscle Trunk	muscle
26	chr19:35848000-35848400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr19:35848200-35848800	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr19:35848200-35849200	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr19:35848200-35849400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr19:35848200-35849600	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr19:35848400-35848800	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr19:35848400-35849000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr19:35848400-35849400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr19:35848400-35849400	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr19:35848400-35849400	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr19:35848400-35849400	Enhancers	Fetal Muscle Leg	muscle
37	chr19:35848400-35849400	Enhancers	HepG2	liver
38	chr19:35848400-35849600	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr19:35848400-35849600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr19:35848400-35849600	Enhancers	Placenta	Placenta
41	chr19:35848600-35848800	Enhancers	Adipose Nuclei	Adipose
42	chr19:35848600-35849000	Enhancers	Fetal Lung	lung
43	chr19:35848600-35849200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr19:35848600-35849400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr19:35848600-35849400	Enhancers	Gastric	stomach
46	chr19:35848600-35849400	Enhancers	Pancreas	Pancrea
47	chr19:35848800-35849000	Enhancers	Fetal Intestine Large	intestine
48	chr19:35848800-35849200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr19:35848800-35849200	Enhancers	Fetal Brain Female	brain
50	chr19:35848800-35849200	Enhancers	Fetal Muscle Trunk	muscle

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