Variant report

Variant	esv2758352
Chromosome Location	chr14:32858480-33016442
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1638)
CpG islands
(count:305)
Chromatin interactive
region (count:36)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1638 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:32938606-32938955	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:32982837-32983067	K562	blood:	n/a	n/a
3	ARID3A	chr14:32982826-32983072	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:32938725-32938910	K562	blood:	n/a	n/a
5	ATF3	chr14:32976879-32977246	HCT-116	colon:	n/a	n/a
6	BACH1	chr14:32953383-32953584	K562	blood:	n/a	n/a
7	BATF	chr14:32904165-32904364	GM12878	blood:	n/a	chr14:32904268-32904279
8	BATF	chr14:32953337-32954435	GM12878	blood:	n/a	n/a
9	BATF	chr14:32904145-32904366	GM12878	blood:	n/a	chr14:32904268-32904279
10	BATF	chr14:32953354-32954358	GM12878	blood:	n/a	n/a
11	BCL11A	chr14:32953284-32954370	GM12878	blood:	n/a	n/a
12	BCL11A	chr14:32953360-32954352	GM12878	blood:	n/a	n/a
13	BHLHE40	chr14:32923585-32923800	GM12878	blood:	n/a	n/a
14	BHLHE40	chr14:32953340-32954372	HepG2	liver:	n/a	n/a
15	BHLHE40	chr14:32903627-32903759	K562	blood:	n/a	n/a
16	BHLHE40	chr14:32953211-32953584	K562	blood:	n/a	n/a
17	BRCA1	chr14:32918960-32919121	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr14:32978806-32979451	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr14:32978742-32979322	MCF-7	breast:	n/a	n/a
20	CEBPB	chr14:32941928-32942312	IMR90	lung:	n/a	n/a
21	CEBPB	chr14:32942654-32943060	MCF-7	breast:	n/a	n/a
22	CEBPB	chr14:32942703-32942960	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:32867191-32867852	Hela-S3	cervix:	n/a	chr14:32867379-32867396 chr14:32867380-32867393 chr14:32867380-32867391 chr14:32867381-32867392
24	CEBPB	chr14:32976917-32977146	K562	blood:	n/a	chr14:32977000-32977011
25	CEBPB	chr14:32978683-32979523	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr14:32882279-32882343	HepG2	liver:	n/a	n/a
27	CEBPB	chr14:32874501-32874639	HepG2	liver:	n/a	chr14:32874614-32874625
28	CEBPB	chr14:32976823-32977255	A549	lung:	n/a	chr14:32977000-32977011
29	CEBPB	chr14:32938112-32938927	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr14:32942683-32942889	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr14:32885302-32885793	HepG2	liver:	n/a	chr14:32885458-32885469
32	CEBPB	chr14:32941994-32942278	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr14:32978807-32979031	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:32976760-32977385	Hela-S3	cervix:	n/a	chr14:32977000-32977011
35	CEBPB	chr14:32976813-32977232	ECC-1	luminal epithelium:	n/a	chr14:32977000-32977011
36	CEBPB	chr14:32938123-32938524	IMR90	lung:	n/a	n/a
37	CEBPB	chr14:32978725-32979367	A549	lung:	n/a	n/a
38	CEBPB	chr14:32976837-32977177	K562	blood:	n/a	chr14:32977000-32977011
39	CEBPB	chr14:32976697-32977307	HCT-116	colon:	n/a	chr14:32977000-32977011
40	CEBPB	chr14:32976785-32977226	MCF-7	breast:	n/a	chr14:32977000-32977011
41	CEBPB	chr14:32867234-32867532	A549	lung:	n/a	chr14:32867379-32867396 chr14:32867380-32867393 chr14:32867380-32867391 chr14:32867381-32867392
42	CEBPB	chr14:32982037-32982244	HepG2	liver:	n/a	chr14:32982148-32982159
43	CEBPB	chr14:32942577-32942991	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr14:32976703-32977362	HCT-116	colon:	n/a	chr14:32977000-32977011
45	CEBPB	chr14:32942693-32942968	A549	lung:	n/a	n/a
46	CEBPB	chr14:32968312-32968527	HepG2	liver:	n/a	chr14:32968482-32968493
47	CEBPB	chr14:32978713-32979518	IMR90	lung:	n/a	n/a
48	CEBPB	chr14:32978748-32979036	A549	lung:	n/a	n/a
49	CEBPB	chr14:32978643-32979280	MCF-7	breast:	n/a	n/a
50	CEBPB	chr14:32867224-32867537	HepG2	liver:	n/a	chr14:32867379-32867396 chr14:32867380-32867393 chr14:32867380-32867391 chr14:32867381-32867392

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:32866773-32866823	HRPEpiC	eye:	n/a
2	chr14:32866773-32866823	MCF-7	breast:	n/a
3	chr14:32866773-32866823	Caco-2	colon:	n/a
4	chr14:32926900-32926950	SK-N-MC	brain:	n/a
5	chr14:32981885-32981935	HMEC	breast:	n/a
6	chr14:32896478-32896528	AG04450	lung:	fetal
7	chr14:32866773-32866823	HEK293	kidney:	embryo
8	chr14:32896478-32896528	U87	brain:	n/a
9	chr14:32981885-32981935	HUVEC	blood vessel:	n/a
10	chr14:32926900-32926950	PFSK-1	brain:	n/a
11	chr14:32866773-32866823	BJ	skin:	n/a
12	chr14:32926900-32926950	CMK	blood:	n/a
13	chr14:32981885-32981935	NHDF-neo	bronchial:	n/a
14	chr14:32941841-32941891	ECC-1	luminal epithelium:	n/a
15	chr14:32981885-32981935	GM06990	blood:	n/a
16	chr14:32896478-32896528	HEK293	kidney:	embryo
17	chr14:32941841-32941891	ovcar-3	ovarian:	n/a
18	chr14:32926900-32926950	Caco-2	colon:	n/a
19	chr14:32896478-32896528	HMEC	breast:	n/a
20	chr14:32981885-32981935	BE2_C	brain:	n/a
21	chr14:32926900-32926950	T-47D	breast:	n/a
22	chr14:32981885-32981935	HEK293	kidney:	embryo
23	chr14:32926900-32926950	HCPEpiC	choroid plexus:	n/a
24	chr14:32941841-32941891	BE2_C	brain:	n/a
25	chr14:32896478-32896528	A549	lung:	n/a
26	chr14:32866773-32866823	ProgFib	skin:	n/a
27	chr14:32896478-32896528	ovcar-3	ovarian:	n/a
28	chr14:32941841-32941891	Jurkat	blood:	n/a
29	chr14:32866773-32866823	NHDF-neo	bronchial:	n/a
30	chr14:32981885-32981935	NB4	blood:	n/a
31	chr14:32926900-32926950	U87	brain:	n/a
32	chr14:32981885-32981935	HCPEpiC	choroid plexus:	n/a
33	chr14:32941841-32941891	CMK	blood:	n/a
34	chr14:32896478-32896528	HAEpiC	amniotic membrane:	n/a
35	chr14:32896478-32896528	SK-N-SH	brain:	n/a
36	chr14:32981885-32981935	HRCEpiC	kidney:	n/a
37	chr14:32941841-32941891	AoSMC	blood vessel:	n/a
38	chr14:32941841-32941891	AG09319	gingival:	n/a
39	chr14:32896478-32896528	AG04449	skin:	fetal
40	chr14:32866773-32866823	Hepatocyte	liver:	n/a
41	chr14:32981885-32981935	HepG2	liver:	n/a
42	chr14:32926900-32926950	MCF-7	breast:	n/a
43	chr14:32866773-32866823	IMR90	lung:	fetal
44	chr14:32896478-32896528	HCF	heart:	n/a
45	chr14:32941841-32941891	HMEC	breast:	n/a
46	chr14:32981885-32981935	U87	brain:	n/a
47	chr14:32926900-32926950	HL-60	blood:	n/a
48	chr14:32981885-32981935	NT2-D1	testis:	n/a
49	chr14:32981885-32981935	SK-N-MC	brain:	n/a
50	chr14:32866773-32866823	GM12891	blood:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:32941433..32942936-chr14:32946433..32948525,2	MCF-7	breast:
2	chr14:32866943..32869881-chr14:32876415..32878628,2	MCF-7	breast:
3	chr14:32936100..32938638-chr14:32940941..32943770,2	K562	blood:
4	chr14:32943721..32945692-chr14:32947594..32949862,2	MCF-7	breast:
5	chr14:32912752..32915224-chr14:32918324..32920883,2	K562	blood:
6	chr14:32901776..32904730-chr14:32922169..32924745,2	MCF-7	breast:
7	chr14:32960517..32962763-chr14:32965947..32968898,2	MCF-7	breast:
8	chr14:32942252..32944730-chr14:32978909..32980551,2	MCF-7	breast:
9	chr14:32851675..32852435-chr14:32982550..32983471,2	MCF-7	breast:
10	chr14:32908071..32910208-chr14:32913357..32914973,2	K562	blood:
11	chr14:32942791..32945014-chr14:32949857..32951632,2	MCF-7	breast:
12	chr14:32908071..32910208-chr14:32913357..32914973,2	K562	blood:
13	chr14:32730953..32733918-chr14:32882288..32884788,2	MCF-7	breast:
14	chr14:32941433..32942936-chr14:32946433..32948525,2	MCF-7	breast:
15	chr14:32854265..32856331-chr14:32866756..32868974,2	MCF-7	breast:
16	chr14:32942325..32944168-chr14:32977022..32979328,2	MCF-7	breast:
17	chr14:32748258..32751049-chr14:32978793..32981637,2	MCF-7	breast:
18	chr14:32842992..32845241-chr14:32865436..32867391,2	MCF-7	breast:
19	chr14:32776960..32777923-chr14:32978540..32979269,2	MCF-7	breast:
20	chr14:32947699..32950524-chr14:32951801..32954077,2	K562	blood:
21	chr14:32904805..32907044-chr14:32912788..32914378,2	K562	blood:
22	chr14:32394986..32395973-chr14:32938340..32938867,2	K562	blood:
23	chr14:32848788..32851684-chr14:32867343..32869134,2	MCF-7	breast:
24	chr14:32943721..32945692-chr14:32947594..32949862,2	MCF-7	breast:
25	chr14:32904805..32907044-chr14:32912788..32914378,2	K562	blood:
26	chr14:32864947..32867000-chr14:32868325..32869881,2	MCF-7	breast:
27	chr14:32960517..32962763-chr14:32965947..32968898,2	MCF-7	breast:
28	chr14:32971520..32973880-chr14:32975639..32977669,2	MCF-7	breast:
29	chr14:32938979..32940480-chr14:32942478..32945273,2	K562	blood:
30	chr14:32862310..32864166-chr14:32889384..32891592,2	MCF-7	breast:
31	chr14:32866943..32869881-chr14:32876415..32878628,2	MCF-7	breast:
32	chr14:32971520..32973880-chr14:32975639..32977669,2	MCF-7	breast:
33	chr14:32902258..32904086-chr14:32906783..32908979,2	MCF-7	breast:
34	chr14:32862310..32864166-chr14:32889384..32891592,2	MCF-7	breast:
35	chr14:32912752..32915224-chr14:32918324..32920883,2	K562	blood:
36	chr14:32864947..32867000-chr14:32868325..32869881,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP5-3	chr14:32914214-32914511	uc_367_+
2	lnc-C14orf126-6	chr14:32872250-32872600	ENSG00000258580.1
3	lnc-C14orf126-6	chr14:32887014-32887169	ENSG00000258580.1
4	lnc-C14orf126-6	chr14:32887014-32887180	ENSG00000258580.1
5	lnc-ARHGAP5-2	chr14:32911547-32911843	NONHSAT036306
6	lnc-C14orf126-11	chr14:32914214-32914511	uc_367_-

No data

Variant related genes	Relation type
ENSG00000259045	TF binding region
ENSG00000258580	TF binding region
AKAP6	TF binding region
RN7SL660P	TF binding region
ENSG00000259045	CpG island
ENSG00000258580	CpG island
AKAP6	CpG island
RN7SL660P	CpG island
ENSG00000259045	chromatin interactions
ENSG00000151320	chromatin interactions

Extended variants
information (count: 6215 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:6215 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183341575	chr14:32858524-32858525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs12896184	chr14:32858565-32858566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1957643	chr14:32858577-32858578	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs112399772	chr14:32858581-32858582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371335059	chr14:32858613-32858614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530094446	chr14:32858633-32858634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372633512	chr14:32858647-32858648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569723381	chr14:32858674-32858675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537265742	chr14:32858679-32858680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558504086	chr14:32858681-32858682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570735077	chr14:32858693-32858694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs377538827	chr14:32858733-32858734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140207519	chr14:32858804-32858805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146949529	chr14:32858822-32858823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574491238	chr14:32858839-32858840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187285167	chr14:32858877-32858878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557037057	chr14:32858879-32858880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567393820	chr14:32858920-32858921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs8021804	chr14:32858943-32858944	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs79046093	chr14:32858981-32858982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374079122	chr14:32858992-32858993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543975769	chr14:32859014-32859015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565186806	chr14:32859047-32859048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs8005778	chr14:32859048-32859049	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs72666181	chr14:32859060-32859061	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs559275684	chr14:32859130-32859131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530128377	chr14:32859132-32859133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35263553	chr14:32859137-32859138	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs563785914	chr14:32859171-32859172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530935060	chr14:32859187-32859188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552395109	chr14:32859251-32859252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142200958	chr14:32859254-32859255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534871512	chr14:32859258-32859259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192009314	chr14:32859297-32859298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111996581	chr14:32859305-32859306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4519249	chr14:32859337-32859338	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs4399468	chr14:32859352-32859353	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs183011126	chr14:32859376-32859377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536063085	chr14:32859385-32859386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556712541	chr14:32859395-32859396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565769411	chr14:32859448-32859449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532148877	chr14:32859477-32859478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575296489	chr14:32859486-32859487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187934792	chr14:32859517-32859518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138673486	chr14:32859544-32859545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs35451285	chr14:32859558-32859559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149311551	chr14:32859569-32859570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373852612	chr14:32859625-32859626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs193001989	chr14:32859635-32859636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143660574	chr14:32859650-32859651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2414 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32849000-32867400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:32854200-32866600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr14:32859400-32859600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr14:32859800-32860200	Enhancers	Left Ventricle	heart
5	chr14:32860000-32860400	Enhancers	Fetal Heart	heart
6	chr14:32860200-32860400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr14:32860200-32860400	Enhancers	Brain Cingulate Gyrus	brain
8	chr14:32860200-32860800	Enhancers	Brain Substantia Nigra	brain
9	chr14:32860200-32865600	Weak transcription	Left Ventricle	heart
10	chr14:32860400-32863800	Weak transcription	Fetal Heart	heart
11	chr14:32860600-32865600	Weak transcription	Brain Hippocampus Middle	brain
12	chr14:32860800-32863600	Weak transcription	Brain Cingulate Gyrus	brain
13	chr14:32860800-32865600	Weak transcription	Brain Substantia Nigra	brain
14	chr14:32862000-32867000	Weak transcription	Brain Germinal Matrix	brain
15	chr14:32862400-32864400	Enhancers	Brain Anterior Caudate	brain
16	chr14:32862600-32863800	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr14:32863400-32863600	Enhancers	Brain Angular Gyrus	brain
18	chr14:32863600-32863800	Enhancers	Brain Cingulate Gyrus	brain
19	chr14:32863600-32865400	Weak transcription	Brain Angular Gyrus	brain
20	chr14:32863800-32864000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
21	chr14:32863800-32864400	Enhancers	Fetal Heart	heart
22	chr14:32863800-32865000	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr14:32863800-32865400	Weak transcription	Brain Cingulate Gyrus	brain
24	chr14:32864000-32865400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr14:32864200-32864400	Enhancers	Psoas Muscle	Psoas
26	chr14:32864400-32865400	Weak transcription	Brain Anterior Caudate	brain
27	chr14:32864400-32866800	Weak transcription	Fetal Heart	heart
28	chr14:32865000-32867800	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr14:32865400-32865600	Enhancers	Fetal Brain Male	brain
30	chr14:32865400-32865800	Enhancers	Esophagus	oesophagus
31	chr14:32865400-32866200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr14:32865400-32868000	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr14:32865400-32868000	Enhancers	Brain Angular Gyrus	brain
34	chr14:32865400-32868800	Enhancers	Brain Cingulate Gyrus	brain
35	chr14:32865400-32871400	Enhancers	Brain Anterior Caudate	brain
36	chr14:32865600-32865800	Enhancers	Brain Substantia Nigra	brain
37	chr14:32865600-32865800	Enhancers	Left Ventricle	heart
38	chr14:32865600-32866200	Enhancers	H1 Cell Line	embryonic stem cell
39	chr14:32865600-32866200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr14:32865600-32866400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr14:32865600-32866800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr14:32865600-32868000	Enhancers	NHEK	skin
43	chr14:32865600-32868400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr14:32865600-32868800	Enhancers	Brain Hippocampus Middle	brain
45	chr14:32865600-32876400	Weak transcription	Fetal Brain Male	brain
46	chr14:32865800-32866000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr14:32865800-32866200	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr14:32865800-32866200	Weak transcription	Brain Substantia Nigra	brain
49	chr14:32865800-32866200	Weak transcription	Left Ventricle	heart
50	chr14:32866000-32866400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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