Variant report

Variant	nsv911235
Chromosome Location	chr19:18143862-18175853
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1010)
CpG islands
(count:61)
Chromatin interactive
region (count:60)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1010 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:18169252-18169439	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:18175633-18176000	K562	blood:	n/a	n/a
3	ARID3A	chr19:18156938-18157043	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:18175679-18175969	HepG2	liver:	n/a	n/a
5	ARID3A	chr19:18169228-18169431	K562	blood:	n/a	n/a
6	ATF1	chr19:18175640-18175930	K562	blood:	n/a	n/a
7	ATF2	chr19:18155620-18156249	GM12878	blood:	n/a	n/a
8	ATF2	chr19:18155717-18156252	GM12878	blood:	n/a	n/a
9	ATF2	chr19:18169102-18169542	GM12878	blood:	n/a	n/a
10	ATF3	chr19:18171353-18171614	K562	blood:	n/a	n/a
11	ATF3	chr19:18171317-18171571	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr19:18156879-18157065	K562	blood:	n/a	n/a
13	ATF3	chr19:18156805-18157204	K562	blood:	n/a	n/a
14	BACH1	chr19:18169360-18169616	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr19:18155768-18156198	GM12878	blood:	n/a	n/a
16	BCL11A	chr19:18155699-18156154	GM12878	blood:	n/a	n/a
17	BCL11A	chr19:18155760-18156149	GM12878	blood:	n/a	n/a
18	BCL3	chr19:18146235-18146561	GM12878	blood:	n/a	n/a
19	BCL3	chr19:18155727-18156267	GM12878	blood:	n/a	n/a
20	BCLAF1	chr19:18155631-18156249	GM12878	blood:	n/a	n/a
21	BCLAF1	chr19:18155664-18156227	GM12878	blood:	n/a	n/a
22	BHLHE40	chr19:18168561-18168583	K562	blood:	n/a	n/a
23	BHLHE40	chr19:18169189-18169484	GM12878	blood:	n/a	n/a
24	BHLHE40	chr19:18157728-18157823	HepG2	liver:	n/a	n/a
25	BHLHE40	chr19:18166610-18166826	K562	blood:	n/a	n/a
26	BHLHE40	chr19:18156054-18156110	K562	blood:	n/a	n/a
27	BHLHE40	chr19:18175644-18176001	K562	blood:	n/a	n/a
28	BHLHE40	chr19:18155751-18156179	GM12878	blood:	n/a	chr19:18155910-18155926
29	BRCA1	chr19:18173108-18173243	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr19:18169187-18169401	GM12878	blood:	n/a	n/a
31	BRCA1	chr19:18169105-18169499	H1-hESC	embryonic stem cell:	n/a	n/a
32	CBX3	chr19:18175502-18176018	K562	blood:	n/a	n/a
33	CBX3	chr19:18166760-18167066	K562	blood:	n/a	n/a
34	CBX3	chr19:18174200-18174833	K562	blood:	n/a	n/a
35	CBX3	chr19:18171179-18171708	K562	blood:	n/a	n/a
36	CBX3	chr19:18169134-18169441	K562	blood:	n/a	n/a
37	CBX3	chr19:18155759-18156479	K562	blood:	n/a	n/a
38	CBX3	chr19:18174360-18174742	K562	blood:	n/a	n/a
39	CCNT2	chr19:18155985-18156076	K562	blood:	n/a	n/a
40	CCNT2	chr19:18169054-18169414	K562	blood:	n/a	chr19:18169167-18169176
41	CEBPB	chr19:18145963-18146223	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr19:18169170-18169522	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr19:18167502-18167718	HepG2	liver:	n/a	n/a
44	CEBPB	chr19:18155945-18156014	HepG2	liver:	n/a	n/a
45	CEBPB	chr19:18167494-18167681	A549	lung:	n/a	n/a
46	CEBPB	chr19:18169277-18169322	HepG2	liver:	n/a	n/a
47	CEBPB	chr19:18175651-18175879	K562	blood:	n/a	n/a
48	CEBPB	chr19:18155666-18156078	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr19:18150466-18150549	IMR90	lung:	n/a	n/a
50	CEBPB	chr19:18156836-18157225	Hela-S3	cervix:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18170383-18170433	Caco-2	colon:	n/a
2	chr19:18170383-18170433	PANC-1	pancreas:	n/a
3	chr19:18170383-18170433	AG10803	skin:	n/a
4	chr19:18170383-18170433	BJ	skin:	n/a
5	chr19:18170383-18170433	HL-60	blood:	n/a
6	chr19:18170383-18170433	Jurkat	blood:	n/a
7	chr19:18170383-18170433	Hepatocyte	liver:	n/a
8	chr19:18170383-18170433	AG09319	gingival:	n/a
9	chr19:18170383-18170433	SAEC	small airway:	n/a
10	chr19:18170383-18170433	U87	brain:	n/a
11	chr19:18170383-18170433	AG04450	lung:	fetal
12	chr19:18170383-18170433	GM19239	blood:	n/a
13	chr19:18170383-18170433	SK-N-SH	brain:	n/a
14	chr19:18170383-18170433	HCM	heart:	n/a
15	chr19:18170383-18170433	NHDF-neo	bronchial:	n/a
16	chr19:18170383-18170433	HUVEC	blood vessel:	n/a
17	chr19:18170383-18170433	HEEpiC	esophagus:	n/a
18	chr19:18170383-18170433	GM12891	blood:	n/a
19	chr19:18170383-18170433	CMK	blood:	n/a
20	chr19:18170383-18170433	NT2-D1	testis:	n/a
21	chr19:18170383-18170433	HepG2	liver:	n/a
22	chr19:18170383-18170433	MCF-7	breast:	n/a
23	chr19:18170383-18170433	HMEC	breast:	n/a
24	chr19:18170383-18170433	HRCEpiC	kidney:	n/a
25	chr19:18170383-18170433	HIPEpiC	eye:	n/a
26	chr19:18170383-18170433	ovcar-3	ovarian:	n/a
27	chr19:18170383-18170433	HCPEpiC	choroid plexus:	n/a
28	chr19:18170383-18170433	SKMC	muscle:	n/a
29	chr19:18170383-18170433	MCF10A-Er-Src	breast:	n/a
30	chr19:18170383-18170433	HRPEpiC	eye:	n/a
31	chr19:18170383-18170433	AoSMC	blood vessel:	n/a
32	chr19:18170383-18170433	ProgFib	skin:	n/a
33	chr19:18170383-18170433	HCF	heart:	n/a
34	chr19:18170383-18170433	NH-A	brain:	n/a
35	chr19:18170383-18170433	NB4	blood:	n/a
36	chr19:18170383-18170433	A549	lung:	n/a
37	chr19:18170383-18170433	GM12892	blood:	n/a
38	chr19:18170383-18170433	BE2_C	brain:	n/a
39	chr19:18170383-18170433	AG04449	skin:	fetal
40	chr19:18170383-18170433	HNPCEpiC	eye:	n/a
41	chr19:18170383-18170433	SK-N-SH_RA	brain:	n/a
42	chr19:18170383-18170433	GM06990	blood:	n/a
43	chr19:18170383-18170433	Hela-S3	cervix:	n/a
44	chr19:18170383-18170433	ECC-1	luminal epithelium:	n/a
45	chr19:18170383-18170433	HPAEpiC	pulmonary alveolar:	n/a
46	chr19:18170383-18170433	NHBE	bronchial:	n/a
47	chr19:18170383-18170433	LNCaP	prostate:	n/a
48	chr19:18170383-18170433	PFSK-1	brain:	n/a
49	chr19:18170383-18170433	HRE	kidney:	n/a
50	chr19:18170383-18170433	HCT-116	colon:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr19:18116678..18118349-chr19:18169310..18171624,2	MCF-7	breast:
2	chr19:18162504..18164365-chr19:18167164..18169094,2	MCF-7	breast:
3	chr19:18168352..18169931-chr19:18171627..18174496,2	K562	blood:
4	chr19:18154267..18157193-chr19:18263191..18265288,2	MCF-7	breast:
5	chr19:18116444..18119992-chr19:18166897..18169714,4	K562	blood:
6	chr19:18156076..18159856-chr19:18160946..18164274,3	MCF-7	breast:
7	chr19:18175848..18177697-chr19:18184239..18186730,2	MCF-7	breast:
8	chr19:17980924..17981724-chr19:18168905..18169800,4	K562	blood:
9	chr19:18129262..18132278-chr19:18167782..18169896,3	K562	blood:
10	chr19:18167851..18170563-chr19:18548504..18551321,2	K562	blood:
11	chr19:18134200..18136668-chr19:18153493..18156113,3	MCF-7	breast:
12	chr19:18162504..18164365-chr19:18167164..18169094,2	MCF-7	breast:
13	chr19:18172332..18174295-chr19:18269343..18271118,2	K562	blood:
14	chr19:18155898..18158519-chr19:18160810..18162412,2	MCF-7	breast:
15	chr19:18111782..18114682-chr19:18163149..18164726,2	MCF-7	breast:
16	chr19:18121912..18124074-chr19:18160321..18162815,2	K562	blood:
17	chr19:18161070..18163836-chr19:18165980..18167646,2	MCF-7	breast:
18	chr19:18108637..18109581-chr19:18168824..18169425,2	K562	blood:
19	chr19:18175810..18177346-chr19:18219359..18221194,2	MCF-7	breast:
20	chr19:18168077..18170768-chr19:18203861..18205779,2	K562	blood:
21	chr19:18117524..18118497-chr19:18170482..18171294,2	K562	blood:
22	chr1:46152203..46153086-chr19:18168643..18169301,2	HCT-116	colon:
23	chr19:17982398..17985046-chr19:18164671..18167194,2	K562	blood:
24	chr19:18151208..18152870-chr19:18153023..18154573,2	MCF-7	breast:
25	chr19:18110500..18112488-chr19:18174652..18177496,3	MCF-7	breast:
26	chr19:18155898..18158519-chr19:18160810..18162412,2	MCF-7	breast:
27	chr19:18164213..18165777-chr19:18168109..18169737,2	K562	blood:
28	chr19:18151513..18153338-chr19:18153517..18156090,2	K562	blood:
29	chr19:18173990..18174805-chr19:18278703..18279468,3	K562	blood:
30	chr19:18117512..18118471-chr19:18168887..18169895,16	K562	blood:
31	chr19:18168352..18169931-chr19:18171627..18174496,2	K562	blood:
32	chr19:18164213..18165777-chr19:18168109..18169737,2	K562	blood:
33	chr19:18131330..18133066-chr19:18154665..18156439,2	MCF-7	breast:
34	chr19:18112057..18114100-chr19:18169438..18171511,2	MCF-7	breast:
35	chr19:18123288..18126278-chr19:18168683..18170920,3	K562	blood:
36	chr19:18110575..18113345-chr19:18155662..18157474,2	K562	blood:
37	chr19:18116206..18122665-chr19:18167802..18171424,9	MCF-7	breast:
38	chr19:18131558..18133664-chr19:18149672..18151270,2	K562	blood:
39	chr19:18117507..18118415-chr19:18168554..18169803,7	MCF-7	breast:
40	chr19:18151208..18152870-chr19:18153023..18154573,2	MCF-7	breast:
41	chr19:18151285..18154107-chr19:18157789..18160364,2	MCF-7	breast:
42	chr19:17976091..17978002-chr19:18142609..18145534,2	K562	blood:
43	chr19:18117457..18120181-chr19:18166897..18171800,6	K562	blood:
44	chr19:18174502..18178222-chr19:18262412..18264976,3	K562	blood:
45	chr19:18161070..18163836-chr19:18165980..18167646,2	MCF-7	breast:
46	chr19:18146460..18148866-chr19:18158094..18160600,2	MCF-7	breast:
47	chr19:18117408..18118699-chr19:18168880..18170084,19	MCF-7	breast:
48	chr19:18117511..18118459-chr19:18170615..18171118,2	MCF-7	breast:
49	chr19:18110512..18113596-chr19:18166649..18169173,4	MCF-7	breast:
50	chr19:18142049..18143591-chr19:18151650..18154095,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARRDC2-2	chr19:18159447-18159888	NONHSAT062934
2	lnc-ARRDC2-1	chr19:18151203-18151866	NONHSAT062933

No data

Variant related genes	Relation type
ENSG00000268623	TF binding region
RPS18P13	TF binding region
ENSG00000268623	CpG island
RPS18P13	CpG island
ENSG00000105647	chromatin interactions
ENSG00000268032	chromatin interactions
ENSG00000105655	chromatin interactions
ENSG00000268173	chromatin interactions
ENSG00000105641	chromatin interactions
ENSG00000216490	chromatin interactions
ENSG00000099308	chromatin interactions
ENSG00000243455	chromatin interactions
ENSG00000159592	chromatin interactions
ENSG00000159596	chromatin interactions
ENSG00000105643	chromatin interactions
ENSG00000269145	chromatin interactions

Extended variants
information (count: 1446 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1446 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11883085	chr19:18143862-18143863	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs528511922	chr19:18143868-18143869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548311180	chr19:18143884-18143885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568427830	chr19:18143904-18143905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs35627700	chr19:18143954-18143955	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs570440333	chr19:18143956-18143957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs367922278	chr19:18143988-18143989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73925409	chr19:18143993-18143994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569913024	chr19:18143998-18143999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538446192	chr19:18144058-18144059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs80282613	chr19:18144090-18144091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553717372	chr19:18144097-18144098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184533430	chr19:18144110-18144111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574376415	chr19:18144128-18144129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs535672848	chr19:18144160-18144161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554153567	chr19:18144180-18144181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574050975	chr19:18144246-18144247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190282857	chr19:18144252-18144253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563632686	chr19:18144254-18144255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532778618	chr19:18144312-18144313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546056134	chr19:18144320-18144321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559867212	chr19:18144447-18144448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145405524	chr19:18144494-18144495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149147718	chr19:18144497-18144498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568466696	chr19:18144502-18144503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs146327909	chr19:18144511-18144512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550138706	chr19:18144546-18144547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147869280	chr19:18144572-18144573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs181527896	chr19:18144589-18144590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141664487	chr19:18144590-18144591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35999299	chr19:18144633-18144634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs55819139	chr19:18144660-18144661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557414800	chr19:18144661-18144662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs565829103	chr19:18144677-18144678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs550223374	chr19:18144793-18144794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs58115391	chr19:18144811-18144812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371027076	chr19:18144823-18144824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554243261	chr19:18144861-18144862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574137577	chr19:18144894-18144895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536636519	chr19:18144934-18144935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs377226747	chr19:18144961-18144962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs397828340	chr19:18144974-18144975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs557262691	chr19:18145006-18145007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577487559	chr19:18145012-18145013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186661623	chr19:18145014-18145015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559705277	chr19:18145023-18145024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544674690	chr19:18145038-18145039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557804505	chr19:18145075-18145076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542387321	chr19:18145156-18145157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs562154585	chr19:18145164-18145165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Follicular lymphoma	20505157	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	20179077	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Lung cancer	17297452	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Chordoma	18071362	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21364760	CNVD
Mycobacterial infection	18421352	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute monocytic leukemia	16498392	CNVD
Lung cancer	18438408	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Liver carcinoma	19366792	CNVD
Colorectal cancer	19455253	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Cancer	17440070	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	17875760	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1095 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18135000-18145400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr19:18135200-18162000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:18135600-18146200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr19:18139200-18144000	Enhancers	Liver	Liver
5	chr19:18139600-18144000	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr19:18139600-18146800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr19:18140200-18144400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr19:18141000-18145800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr19:18141000-18154400	Weak transcription	Right Ventricle	heart
10	chr19:18141200-18145000	Weak transcription	Hela-S3	cervix
11	chr19:18141200-18149400	Weak transcription	Right Atrium	heart
12	chr19:18142400-18146000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr19:18142600-18145800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr19:18142600-18151200	Weak transcription	Esophagus	oesophagus
15	chr19:18142600-18154200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr19:18142800-18145000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr19:18142800-18145400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr19:18142800-18145600	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr19:18142800-18145600	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr19:18142800-18145800	Weak transcription	Primary T cells from cord blood	blood
21	chr19:18142800-18145800	Weak transcription	Duodenum Mucosa	Duodenum
22	chr19:18142800-18145800	Weak transcription	Spleen	Spleen
23	chr19:18142800-18146000	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr19:18143400-18144200	Weak transcription	Brain Anterior Caudate	brain
25	chr19:18143400-18144800	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr19:18143400-18155200	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr19:18143600-18144000	Weak transcription	Primary hematopoietic stem cells	blood
28	chr19:18143800-18145800	Weak transcription	Fetal Thymus	thymus
29	chr19:18144000-18144200	Enhancers	Primary hematopoietic stem cells	blood
30	chr19:18144000-18145400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr19:18144200-18144400	Enhancers	Brain Anterior Caudate	brain
32	chr19:18144200-18155600	Weak transcription	Primary hematopoietic stem cells	blood
33	chr19:18144400-18144800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr19:18144800-18146600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr19:18144800-18146800	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr19:18145000-18146600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr19:18145000-18146600	Enhancers	Hela-S3	cervix
38	chr19:18145400-18146200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr19:18145400-18146600	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr19:18145400-18146800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr19:18145600-18146400	Enhancers	Primary T cells fromperipheralblood	blood
42	chr19:18145600-18146400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr19:18145600-18146400	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr19:18145600-18146400	Enhancers	NHEK	skin
45	chr19:18145800-18146000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr19:18145800-18146200	Enhancers	Duodenum Mucosa	Duodenum
47	chr19:18145800-18146200	Enhancers	Spleen	Spleen
48	chr19:18145800-18146200	Enhancers	HMEC	breast
49	chr19:18145800-18146400	Enhancers	Primary T cells from cord blood	blood
50	chr19:18145800-18146400	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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