Variant report

Variant	nsv1064140
Chromosome Location	chr19:41454790-41516389
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	chr19:41486058-41486085	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:41507311-41507499	K562	blood:	n/a	n/a
4	ATF1	chr19:41468671-41468771	K562	blood:	n/a	n/a
5	ATF3	chr19:41506140-41506734	HCT-116	colon:	n/a	n/a
6	ATF3	chr19:41506267-41506508	K562	blood:	n/a	n/a
7	ATF3	chr19:41506069-41506786	HCT-116	colon:	n/a	n/a
8	ATF3	chr19:41468329-41468885	A549	lung:	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	chr19:41505993-41506787	HCT-116	colon:	n/a	n/a
17	CBX3	chr19:41460404-41460899	K562	blood:	n/a	n/a
18	CEBPB	chr19:41488308-41488880	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
19	CEBPB	chr19:41507152-41507489	K562	blood:	n/a	n/a
20	CEBPB	chr19:41468360-41468789	A549	lung:	n/a	n/a
21	CEBPB	chr19:41506884-41506987	IMR90	lung:	n/a	n/a
22	CEBPB	chr19:41506268-41506934	HepG2	liver:	n/a	chr19:41506435-41506446
23	CEBPB	chr19:41506284-41507442	A549	lung:	n/a	chr19:41506435-41506446
24	CEBPB	chr19:41488434-41488797	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
25	CEBPB	chr19:41506068-41507138	HCT-116	colon:	n/a	chr19:41506435-41506446
26	CEBPB	chr19:41506205-41506669	MCF-7	breast:	n/a	chr19:41506435-41506446
27	CEBPB	chr19:41486382-41486422	K562	blood:	n/a	n/a
28	CEBPB	chr19:41506189-41507135	A549	lung:	n/a	chr19:41506435-41506446
29	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
30	CEBPB	chr19:41505976-41507518	HCT-116	colon:	n/a	chr19:41506435-41506446
31	CEBPB	chr19:41506244-41506603	ECC-1	luminal epithelium:	n/a	chr19:41506435-41506446
32	CEBPB	chr19:41468308-41469019	Hela-S3	cervix:	n/a	chr19:41468797-41468810
33	CEBPB	chr19:41468301-41468559	HepG2	liver:	n/a	n/a
34	CEBPB	chr19:41506263-41507465	K562	blood:	n/a	chr19:41506435-41506446
35	CEBPB	chr19:41488441-41488804	IMR90	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
36	CEBPB	chr19:41506208-41506618	A549	lung:	n/a	chr19:41506435-41506446
37	CEBPB	chr19:41488408-41488845	MCF-7	breast:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
38	CEBPB	chr19:41488522-41488635	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
39	CEBPB	chr19:41488481-41488681	Hela-S3	cervix:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
40	CEBPB	chr19:41468165-41469078	A549	lung:	n/a	chr19:41468797-41468810
41	CEBPB	chr19:41486262-41486477	HepG2	liver:	n/a	n/a
42	CEBPB	chr19:41507207-41507407	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr19:41488438-41488777	K562	blood:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
44	CEBPB	chr19:41488422-41488791	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
45	CEBPB	chr19:41506256-41506628	Hela-S3	cervix:	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	chr19:41486321-41486531	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr19:41468563-41468752	A549	lung:	n/a	n/a
50	CREB1	chr19:41507218-41507529	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41496749-41496799	HRPEpiC	eye:	n/a
2	chr19:41510272-41510322	SKMC	muscle:	n/a
3	chr19:41510285-41510335	HIPEpiC	eye:	n/a
4	chr19:41496749-41496799	HRPEpiC	eye:	n/a
5	chr19:41510272-41510322	SKMC	muscle:	n/a
6	chr19:41510285-41510335	HIPEpiC	eye:	n/a
7	chr19:41497222-41497272	AG09309	skin:	n/a
8	chr19:41510285-41510335	NB4	blood:	n/a
9	chr19:41510026-41510076	IMR90	lung:	fetal
10	chr19:41510026-41510076	GM12891	blood:	n/a
11	chr19:41495942-41495992	A549	lung:	n/a
12	chr19:41510037-41510087	Caco-2	colon:	n/a
13	chr19:41510272-41510322	GM19239	blood:	n/a
14	chr19:41496043-41496093	HEEpiC	esophagus:	n/a
15	chr19:41510026-41510076	Jurkat	blood:	n/a
16	chr19:41510243-41510293	AG04449	skin:	fetal
17	chr19:41496043-41496093	A549	lung:	n/a
18	chr19:41510272-41510322	LNCaP	prostate:	n/a
19	chr19:41497222-41497272	HEEpiC	esophagus:	n/a
20	chr19:41510285-41510335	GM12892	blood:	n/a
21	chr19:41510037-41510087	HNPCEpiC	eye:	n/a
22	chr19:41496043-41496093	GM12891	blood:	n/a
23	chr19:41495942-41495992	ovcar-3	ovarian:	n/a
24	chr19:41510285-41510335	A549	lung:	n/a
25	chr19:41510098-41510148	LNCaP	prostate:	n/a
26	chr19:41496043-41496093	AG04450	lung:	fetal
27	chr19:41495942-41495992	HAEpiC	amniotic membrane:	n/a
28	chr19:41510037-41510087	AG09319	gingival:	n/a
29	chr19:41510098-41510148	HAEpiC	amniotic membrane:	n/a
30	chr19:41510037-41510087	HCT-116	colon:	n/a
31	chr19:41510059-41510109	ECC-1	luminal epithelium:	n/a
32	chr19:41510243-41510293	BE2_C	brain:	n/a
33	chr19:41510026-41510076	HUVEC	blood vessel:	n/a
34	chr19:41496043-41496093	U87	brain:	n/a
35	chr19:41510098-41510148	SK-N-SH_RA	brain:	n/a
36	chr19:41510285-41510335	PFSK-1	brain:	n/a
37	chr19:41510272-41510322	BE2_C	brain:	n/a
38	chr19:41497222-41497272	K562	blood:	n/a
39	chr19:41510243-41510293	HL-60	blood:	n/a
40	chr19:41510059-41510109	K562	blood:	n/a
41	chr19:41495942-41495992	H1-hESC	embryonic stem cell:	embryo
42	chr19:41496749-41496799	SK-N-SH_RA	brain:	n/a
43	chr19:41510285-41510335	HCT-116	colon:	n/a
44	chr19:41495942-41495992	ProgFib	skin:	n/a
45	chr19:41495942-41495992	PANC-1	pancreas:	n/a
46	chr19:41510285-41510335	SK-N-SH	brain:	n/a
47	chr19:41497222-41497272	SAEC	small airway:	n/a
48	chr19:41510272-41510322	HIPEpiC	eye:	n/a
49	chr19:41495942-41495992	HepG2	liver:	n/a
50	chr19:41510037-41510087	IMR90	lung:	fetal

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

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

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

Extended variants
information (count: 2478 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2478 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533341642	chr19:41454792-41454793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551569842	chr19:41454823-41454824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544610644	chr19:41454851-41454852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560579427	chr19:41454906-41454907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562894654	chr19:41454910-41454911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549071372	chr19:41454923-41454924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567632575	chr19:41454924-41454925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116129340	chr19:41454951-41454952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550293130	chr19:41454957-41454958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs17415113	chr19:41454986-41454987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190006800	chr19:41454991-41454992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553934926	chr19:41454995-41454996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572217915	chr19:41455030-41455031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373544362	chr19:41455049-41455050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536532593	chr19:41455050-41455051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554596339	chr19:41455065-41455066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575987624	chr19:41455122-41455123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543056363	chr19:41455155-41455156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564599687	chr19:41455227-41455228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182238430	chr19:41455247-41455248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545171274	chr19:41455277-41455278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73557146	chr19:41455281-41455282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187999264	chr19:41455291-41455292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543281373	chr19:41455306-41455307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199986255	chr19:41455344-41455345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555077648	chr19:41455376-41455377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575422867	chr19:41455378-41455379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561470955	chr19:41455403-41455404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs193224809	chr19:41455413-41455414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199889513	chr19:41455477-41455478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550207716	chr19:41455529-41455530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185236423	chr19:41455591-41455592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546414661	chr19:41455602-41455603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547610471	chr19:41455622-41455623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566298880	chr19:41455633-41455634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188505615	chr19:41455639-41455640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192713419	chr19:41455640-41455641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185074295	chr19:41455649-41455650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560803542	chr19:41455696-41455697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138003505	chr19:41455704-41455705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536604462	chr19:41455726-41455727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535187447	chr19:41455752-41455753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576497946	chr19:41455792-41455793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536451626	chr19:41455804-41455805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369993804	chr19:41455805-41455806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12972933	chr19:41455816-41455817	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs565618104	chr19:41455819-41455820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532807080	chr19:41455834-41455835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552817373	chr19:41455845-41455846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572595757	chr19:41455885-41455886	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:262 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41444800-41455800	Weak transcription	Fetal Intestine Large	intestine
2	chr19:41451800-41455200	Weak transcription	Liver	Liver
3	chr19:41451800-41456200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr19:41451800-41456200	Weak transcription	Fetal Intestine Small	intestine
5	chr19:41453800-41458200	Weak transcription	Right Atrium	heart
6	chr19:41456200-41456400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr19:41459600-41460800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
8	chr19:41460000-41460800	ZNF genes & repeats	Brain Hippocampus Middle	brain
9	chr19:41460000-41461600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr19:41460200-41460400	ZNF genes & repeats	A549	lung
11	chr19:41460200-41461400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
12	chr19:41464600-41464800	Enhancers	Fetal Intestine Small	intestine
13	chr19:41464800-41466400	Weak transcription	Fetal Intestine Small	intestine
14	chr19:41465200-41466600	Enhancers	Esophagus	oesophagus
15	chr19:41465400-41465800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
16	chr19:41465400-41465800	Active TSS	Breast Myoepithelial Primary Cells	Breast
17	chr19:41465400-41466000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr19:41465800-41466000	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr19:41465800-41466000	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
20	chr19:41465800-41466200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr19:41465800-41466200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
22	chr19:41465800-41466200	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
23	chr19:41466000-41466200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr19:41466000-41466200	Bivalent Enhancer	Adipose Nuclei	Adipose
25	chr19:41466000-41466200	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
26	chr19:41466200-41466600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
27	chr19:41466200-41466600	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr19:41466200-41466800	Enhancers	Adipose Nuclei	Adipose
29	chr19:41466200-41469800	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr19:41466200-41469800	Enhancers	Ovary	ovary
31	chr19:41466400-41466600	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr19:41466400-41466800	Enhancers	Fetal Intestine Large	intestine
33	chr19:41466400-41466800	Enhancers	Fetal Intestine Small	intestine
34	chr19:41466600-41468000	Weak transcription	Esophagus	oesophagus
35	chr19:41466800-41467000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
36	chr19:41466800-41467000	Bivalent Enhancer	A549	lung
37	chr19:41466800-41467200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
38	chr19:41466800-41468000	Weak transcription	Adipose Nuclei	Adipose
39	chr19:41467800-41468000	Bivalent Enhancer	A549	lung
40	chr19:41467800-41469600	Enhancers	HepG2	liver
41	chr19:41467800-41469800	Enhancers	Hela-S3	cervix
42	chr19:41468000-41468200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
43	chr19:41468000-41468200	Enhancers	Esophagus	oesophagus
44	chr19:41468000-41468200	Enhancers	Placenta	Placenta
45	chr19:41468000-41468200	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
46	chr19:41468000-41468400	Flanking Bivalent TSS/Enh	A549	lung
47	chr19:41468000-41469400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr19:41468000-41469800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr19:41468000-41469800	Enhancers	Adipose Nuclei	Adipose
50	chr19:41468200-41469600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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