Variant report

Variant	nsv1059607
Chromosome Location	chr19:41456632-41513333
allele	n/a
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	ARID3A	chr19:41506351-41506450	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:41507311-41507499	K562	blood:	n/a	n/a
3	ARID3A	chr19:41486058-41486085	HepG2	liver:	n/a	n/a
4	ATF1	chr19:41468671-41468771	K562	blood:	n/a	n/a
5	ATF3	chr19:41506069-41506786	HCT-116	colon:	n/a	n/a
6	ATF3	chr19:41506140-41506734	HCT-116	colon:	n/a	n/a
7	ATF3	chr19:41468329-41468885	A549	lung:	n/a	n/a
8	ATF3	chr19:41506267-41506508	K562	blood:	n/a	n/a
9	BACH1	chr19:41488176-41489166	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr19:41468291-41469001	A549	lung:	n/a	n/a
11	BCL3	chr19:41468223-41469050	A549	lung:	n/a	n/a
12	BHLHE40	chr19:41507420-41507421	K562	blood:	n/a	n/a
13	BRCA1	chr19:41465957-41466156	GM12878	blood:	n/a	n/a
14	CBX3	chr19:41482345-41482685	K562	blood:	n/a	n/a
15	CBX3	chr19:41460434-41460907	K562	blood:	n/a	n/a
16	CBX3	chr19:41460404-41460899	K562	blood:	n/a	n/a
17	CBX3	chr19:41505993-41506787	HCT-116	colon:	n/a	n/a
18	CEBPB	chr19:41488440-41489019	H1-hESC	embryonic stem cell:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
19	CEBPB	chr19:41468308-41469019	Hela-S3	cervix:	n/a	chr19:41468797-41468810
20	CEBPB	chr19:41488408-41488845	MCF-7	breast:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
21	CEBPB	chr19:41506205-41506669	MCF-7	breast:	n/a	chr19:41506435-41506446
22	CEBPB	chr19:41488308-41488880	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
23	CEBPB	chr19:41506256-41506628	Hela-S3	cervix:	n/a	chr19:41506435-41506446
24	CEBPB	chr19:41506068-41507138	HCT-116	colon:	n/a	chr19:41506435-41506446
25	CEBPB	chr19:41488422-41488791	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
26	CEBPB	chr19:41468165-41469078	A549	lung:	n/a	chr19:41468797-41468810
27	CEBPB	chr19:41506884-41506987	IMR90	lung:	n/a	n/a
28	CEBPB	chr19:41488438-41488777	K562	blood:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
29	CEBPB	chr19:41506208-41506618	A549	lung:	n/a	chr19:41506435-41506446
30	CEBPB	chr19:41506284-41507442	A549	lung:	n/a	chr19:41506435-41506446
31	CEBPB	chr19:41488481-41488681	Hela-S3	cervix:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
32	CEBPB	chr19:41486262-41486477	HepG2	liver:	n/a	n/a
33	CEBPB	chr19:41486382-41486422	K562	blood:	n/a	n/a
34	CEBPB	chr19:41506263-41507465	K562	blood:	n/a	chr19:41506435-41506446
35	CEBPB	chr19:41507152-41507489	K562	blood:	n/a	n/a
36	CEBPB	chr19:41488522-41488635	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
37	CEBPB	chr19:41488441-41488804	IMR90	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
38	CEBPB	chr19:41507207-41507407	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr19:41506268-41506934	HepG2	liver:	n/a	chr19:41506435-41506446
40	CEBPB	chr19:41506244-41506603	ECC-1	luminal epithelium:	n/a	chr19:41506435-41506446
41	CEBPB	chr19:41468301-41468559	HepG2	liver:	n/a	n/a
42	CEBPB	chr19:41468360-41468789	A549	lung:	n/a	n/a
43	CEBPB	chr19:41488434-41488797	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
44	CEBPB	chr19:41506189-41507135	A549	lung:	n/a	chr19:41506435-41506446
45	CEBPB	chr19:41505976-41507518	HCT-116	colon:	n/a	chr19:41506435-41506446
46	CEBPD	chr19:41458422-41458815	K562	blood:	n/a	n/a
47	CHD2	chr19:41465957-41466157	K562	blood:	n/a	n/a
48	CREB1	chr19:41507218-41507529	K562	blood:	n/a	n/a
49	CREB1	chr19:41486321-41486531	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr19:41468563-41468752	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41510285-41510335	SK-N-SH_RA	brain:	n/a
2	chr19:41497222-41497272	ECC-1	luminal epithelium:	n/a
3	chr19:41510243-41510293	CMK	blood:	n/a
4	chr19:41496749-41496799	HAEpiC	amniotic membrane:	n/a
5	chr19:41510059-41510109	NT2-D1	testis:	n/a
6	chr19:41510285-41510335	MCF10A-Er-Src	breast:	n/a
7	chr19:41510243-41510293	SKMC	muscle:	n/a
8	chr19:41510026-41510076	K562	blood:	n/a
9	chr19:41510037-41510087	SK-N-MC	brain:	n/a
10	chr19:41495942-41495992	HMEC	breast:	n/a
11	chr19:41510272-41510322	HMEC	breast:	n/a
12	chr19:41497222-41497272	PrEC	prostate:	n/a
13	chr19:41510098-41510148	LNCaP	prostate:	n/a
14	chr19:41496043-41496093	PANC-1	pancreas:	n/a
15	chr19:41496043-41496093	GM06990	blood:	n/a
16	chr19:41496749-41496799	HEEpiC	esophagus:	n/a
17	chr19:41510037-41510087	Hela-S3	cervix:	n/a
18	chr19:41510285-41510335	HRCEpiC	kidney:	n/a
19	chr19:41510059-41510109	T-47D	breast:	n/a
20	chr19:41497222-41497272	U87	brain:	n/a
21	chr19:41496043-41496093	SK-N-MC	brain:	n/a
22	chr19:41496043-41496093	HPAEpiC	pulmonary alveolar:	n/a
23	chr19:41510243-41510293	HCM	heart:	n/a
24	chr19:41510059-41510109	HIPEpiC	eye:	n/a
25	chr19:41495942-41495992	PrEC	prostate:	n/a
26	chr19:41496749-41496799	AG04449	skin:	fetal
27	chr19:41510285-41510335	GM19239	blood:	n/a
28	chr19:41510059-41510109	NHBE	bronchial:	n/a
29	chr19:41510098-41510148	K562	blood:	n/a
30	chr19:41510059-41510109	HL-60	blood:	n/a
31	chr19:41510243-41510293	MCF10A-Er-Src	breast:	n/a
32	chr19:41510272-41510322	HNPCEpiC	eye:	n/a
33	chr19:41496043-41496093	ECC-1	luminal epithelium:	n/a
34	chr19:41496749-41496799	ovcar-3	ovarian:	n/a
35	chr19:41497222-41497272	ProgFib	skin:	n/a
36	chr19:41510059-41510109	SK-N-SH	brain:	n/a
37	chr19:41496043-41496093	LNCaP	prostate:	n/a
38	chr19:41495942-41495992	NH-A	brain:	n/a
39	chr19:41510026-41510076	HCT-116	colon:	n/a
40	chr19:41496749-41496799	HRE	kidney:	n/a
41	chr19:41510059-41510109	SK-N-MC	brain:	n/a
42	chr19:41495942-41495992	AG09319	gingival:	n/a
43	chr19:41510243-41510293	NB4	blood:	n/a
44	chr19:41496043-41496093	NHDF-neo	bronchial:	n/a
45	chr19:41510243-41510293	AG09309	skin:	n/a
46	chr19:41510098-41510148	HEK293	kidney:	embryo
47	chr19:41510037-41510087	GM19239	blood:	n/a
48	chr19:41510037-41510087	HepG2	liver:	n/a
49	chr19:41510243-41510293	Hepatocyte	liver:	n/a
50	chr19:41495942-41495992	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:41489930..41492049-chr19:41494201..41495851,2	K562	blood:
2	chr19:41455358..41456878-chr19:41467418..41469286,2	K562	blood:
3	chr19:41458951..41460963-chr19:41463374..41465958,2	K562	blood:
4	chr19:41455358..41456878-chr19:41467418..41469286,2	K562	blood:
5	chr19:41480412..41481100-chr19:41650028..41650578,2	MCF-7	breast:
6	chr19:41489930..41492049-chr19:41494201..41495851,2	K562	blood:
7	chr19:41463243..41465087-chr19:41467190..41469905,2	K562	blood:
8	chr19:41480596..41481177-chr19:41649752..41650983,4	K562	blood:
9	chr19:41458951..41460963-chr19:41463374..41465958,2	K562	blood:
10	chr19:41463496..41465246-chr19:41466230..41468956,2	K562	blood:
11	chr10:94639799..94640373-chr19:41475219..41475719,2	K562	blood:
12	chr19:41463243..41465087-chr19:41467190..41469905,2	K562	blood:
13	chr19:41463496..41465246-chr19:41466230..41468956,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP2B6-1	chr19:41503762-41503928	l_1687_chr19:41492503-41503928_testes
2	lnc-CYP2B6-1	chr19:41495264-41495408	l_1687_chr19:41492503-41503928_testes
3	lnc-CYP2B6-1	chr19:41493177-41493736	l_1687_chr19:41492503-41503928_testes
4	lnc-CYP2B6-1	chr19:41493956-41494534	l_1687_chr19:41492503-41503928_testes
5	lnc-CYP2B6-1	chr19:41492504-41492600	l_1687_chr19:41492503-41503928_testes

Variant related genes	Relation type
CYP2B6	TF binding region
CYP2B6	CpG island

Extended variants
information (count: 2199 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2199 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577302165	chr19:41456664-41456665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs541077130	chr19:41456714-41456715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183564074	chr19:41456734-41456735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115217768	chr19:41456792-41456793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548333295	chr19:41456793-41456794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563129783	chr19:41456811-41456812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530644164	chr19:41456812-41456813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552047586	chr19:41456824-41456825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556552579	chr19:41456827-41456828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570451778	chr19:41456830-41456831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150849887	chr19:41456862-41456863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4803408	chr19:41456865-41456866	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs568118997	chr19:41456883-41456884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189419580	chr19:41456887-41456888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139319976	chr19:41456911-41456912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561083184	chr19:41456929-41456930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576707004	chr19:41456954-41456955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73557149	chr19:41456955-41456956	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs559255498	chr19:41456962-41456963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577471578	chr19:41456987-41456988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541388870	chr19:41457017-41457018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149978715	chr19:41457028-41457029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574813523	chr19:41457029-41457030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs117061792	chr19:41457040-41457041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35705946	chr19:41457058-41457059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147659168	chr19:41457120-41457121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140738634	chr19:41457130-41457131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535119719	chr19:41457131-41457132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530607151	chr19:41457148-41457149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551959897	chr19:41457159-41457160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563990348	chr19:41457165-41457166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528397259	chr19:41457174-41457175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546540816	chr19:41457192-41457193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535988211	chr19:41457194-41457195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567947425	chr19:41457195-41457196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535480509	chr19:41457196-41457197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550687226	chr19:41457209-41457210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568983752	chr19:41457213-41457214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs537596958	chr19:41457217-41457218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144470012	chr19:41457218-41457219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571093870	chr19:41457225-41457226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534993135	chr19:41457226-41457227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182218815	chr19:41457289-41457290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574734667	chr19:41457290-41457291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541859221	chr19:41457292-41457293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554705931	chr19:41457304-41457305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377629123	chr19:41457305-41457306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556992996	chr19:41457306-41457307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565451467	chr19:41457360-41457361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575336252	chr19:41457371-41457372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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	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
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41453800-41458200	Weak transcription	Right Atrium	heart
2	chr19:41459600-41460800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
3	chr19:41460000-41460800	ZNF genes & repeats	Brain Hippocampus Middle	brain
4	chr19:41460000-41461600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr19:41460200-41460400	ZNF genes & repeats	A549	lung
6	chr19:41460200-41461400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
7	chr19:41464600-41464800	Enhancers	Fetal Intestine Small	intestine
8	chr19:41464800-41466400	Weak transcription	Fetal Intestine Small	intestine
9	chr19:41465200-41466600	Enhancers	Esophagus	oesophagus
10	chr19:41465400-41465800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
11	chr19:41465400-41465800	Active TSS	Breast Myoepithelial Primary Cells	Breast
12	chr19:41465400-41466000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr19:41465800-41466000	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr19:41465800-41466000	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
15	chr19:41465800-41466200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr19:41465800-41466200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
17	chr19:41465800-41466200	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
18	chr19:41466000-41466200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr19:41466000-41466200	Bivalent Enhancer	Adipose Nuclei	Adipose
20	chr19:41466000-41466200	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
21	chr19:41466200-41466600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
22	chr19:41466200-41466600	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr19:41466200-41466800	Enhancers	Adipose Nuclei	Adipose
24	chr19:41466200-41469800	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr19:41466200-41469800	Enhancers	Ovary	ovary
26	chr19:41466400-41466600	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr19:41466400-41466800	Enhancers	Fetal Intestine Large	intestine
28	chr19:41466400-41466800	Enhancers	Fetal Intestine Small	intestine
29	chr19:41466600-41468000	Weak transcription	Esophagus	oesophagus
30	chr19:41466800-41467000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
31	chr19:41466800-41467000	Bivalent Enhancer	A549	lung
32	chr19:41466800-41467200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
33	chr19:41466800-41468000	Weak transcription	Adipose Nuclei	Adipose
34	chr19:41467800-41468000	Bivalent Enhancer	A549	lung
35	chr19:41467800-41469600	Enhancers	HepG2	liver
36	chr19:41467800-41469800	Enhancers	Hela-S3	cervix
37	chr19:41468000-41468200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
38	chr19:41468000-41468200	Enhancers	Esophagus	oesophagus
39	chr19:41468000-41468200	Enhancers	Placenta	Placenta
40	chr19:41468000-41468200	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
41	chr19:41468000-41468400	Flanking Bivalent TSS/Enh	A549	lung
42	chr19:41468000-41469400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr19:41468000-41469800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr19:41468000-41469800	Enhancers	Adipose Nuclei	Adipose
45	chr19:41468200-41469600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr19:41468400-41468600	Active TSS	A549	lung
47	chr19:41468400-41469000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr19:41468600-41468800	Enhancers	Primary T cells fromperipheralblood	blood
49	chr19:41468600-41469000	Flanking Active TSS	A549	lung
50	chr19:41468800-41469400	Enhancers	Osteobl	bone

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