Variant report

Variant	esv2751288
Chromosome Location	chr14:84815330-85704047
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2088)
CpG islands
(count:794)
Chromatin interactive
region (count:27)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2088 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:85589256-85589486	HepG2	liver:	n/a	n/a
2	BACH1	chr14:85290621-85290963	H1-hESC	embryonic stem cell:	n/a	chr14:85290773-85290787
3	BACH1	chr14:84867405-84867544	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr14:85217109-85217295	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr14:84856515-84856522	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr14:85312895-85313097	GM12878	blood:	n/a	chr14:85312997-85313008
7	BCL11A	chr14:84870148-84870389	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr14:84870134-84870311	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr14:85621151-85621340	GM12878	blood:	n/a	n/a
10	BHLHE40	chr14:85312931-85313080	GM12878	blood:	n/a	n/a
11	BHLHE40	chr14:85109885-85110121	HepG2	liver:	n/a	n/a
12	BHLHE40	chr14:85530250-85530337	GM12878	blood:	n/a	n/a
13	BHLHE40	chr14:85504871-85505190	GM12878	blood:	n/a	n/a
14	BRCA1	chr14:85468850-85468851	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr14:84934624-84934852	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr14:85688313-85688514	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr14:85226661-85227146	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr14:84986860-84986967	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr14:85597979-85598064	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr14:85237055-85237216	K562	blood:	n/a	chr14:85237122-85237133
21	CEBPB	chr14:85679835-85680135	HepG2	liver:	n/a	chr14:85679995-85680006
22	CEBPB	chr14:85385558-85385830	H1-hESC	embryonic stem cell:	n/a	chr14:85385677-85385688
23	CEBPB	chr14:85592950-85593190	A549	lung:	n/a	n/a
24	CEBPB	chr14:85383190-85383374	A549	lung:	n/a	chr14:85383210-85383221
25	CEBPB	chr14:85267586-85267905	IMR90	lung:	n/a	chr14:85267745-85267756
26	CEBPB	chr14:84850333-84850612	HepG2	liver:	n/a	chr14:84850480-84850491
27	CEBPB	chr14:85001858-85002213	IMR90	lung:	n/a	n/a
28	CEBPB	chr14:85345568-85345819	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr14:85554610-85554904	A549	lung:	n/a	chr14:85554757-85554768 chr14:85554757-85554768 chr14:85554795-85554806 chr14:85554755-85554766 chr14:85554755-85554768 chr14:85554755-85554768
30	CEBPB	chr14:85506788-85506891	HepG2	liver:	n/a	n/a
31	CEBPB	chr14:85554396-85555163	Hela-S3	cervix:	n/a	chr14:85554757-85554768 chr14:85554757-85554768 chr14:85554795-85554806 chr14:85554755-85554766 chr14:85554755-85554768 chr14:85554755-85554768
32	CEBPB	chr14:84874612-84874747	K562	blood:	n/a	chr14:84874720-84874731
33	CEBPB	chr14:85267628-85267883	H1-hESC	embryonic stem cell:	n/a	chr14:85267745-85267756
34	CEBPB	chr14:85520728-85520988	A549	lung:	n/a	chr14:85520874-85520885
35	CEBPB	chr14:85457510-85457794	A549	lung:	n/a	chr14:85457637-85457650 chr14:85457638-85457649 chr14:85457637-85457650 chr14:85457637-85457650
36	CEBPB	chr14:85323962-85324284	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr14:85152978-85153211	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr14:85349235-85349589	Hela-S3	cervix:	n/a	chr14:85349378-85349389
39	CEBPB	chr14:85554611-85554896	HepG2	liver:	n/a	chr14:85554757-85554768 chr14:85554757-85554768 chr14:85554795-85554806 chr14:85554755-85554766 chr14:85554755-85554768 chr14:85554755-85554768
40	CEBPB	chr14:85237021-85237261	HepG2	liver:	n/a	chr14:85237122-85237133
41	CEBPB	chr14:85598896-85599024	HepG2	liver:	n/a	n/a
42	CEBPB	chr14:85520754-85521010	IMR90	lung:	n/a	chr14:85520874-85520885
43	CEBPB	chr14:84949617-84950134	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr14:85204722-85205034	HepG2	liver:	n/a	chr14:85204860-85204871
45	CEBPB	chr14:85001862-85002233	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr14:85267585-85267910	HepG2	liver:	n/a	chr14:85267745-85267756
47	CEBPB	chr14:85554658-85554927	MCF-7	breast:	n/a	chr14:85554757-85554768 chr14:85554757-85554768 chr14:85554795-85554806 chr14:85554755-85554766 chr14:85554755-85554768 chr14:85554755-85554768
48	CEBPB	chr14:85662899-85663214	A549	lung:	n/a	n/a
49	CEBPB	chr14:85476561-85476863	Hela-S3	cervix:	n/a	chr14:85476660-85476671 chr14:85476623-85476636
50	CEBPB	chr14:85040081-85040371	IMR90	lung:	n/a	chr14:85040241-85040254 chr14:85040241-85040254 chr14:85040241-85040252 chr14:85040242-85040253

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:84903063-84903113	NHDF-neo	bronchial:	n/a
2	chr14:84903063-84903113	NHDF-neo	bronchial:	n/a
3	chr14:85058259-85058309	HCM	heart:	n/a
4	chr14:85010778-85010828	GM19239	blood:	n/a
5	chr14:85292067-85292117	IMR90	lung:	fetal
6	chr14:85010778-85010828	A549	lung:	n/a
7	chr14:84965587-84965637	NB4	blood:	n/a
8	chr14:85214861-85214911	AG09309	skin:	n/a
9	chr14:85292067-85292117	HMEC	breast:	n/a
10	chr14:85214861-85214911	GM12892	blood:	n/a
11	chr14:84978099-84978149	HCPEpiC	choroid plexus:	n/a
12	chr14:84903063-84903113	NT2-D1	testis:	n/a
13	chr14:85667733-85667783	MCF-7	breast:	n/a
14	chr14:84903063-84903113	SK-N-SH	brain:	n/a
15	chr14:85058259-85058309	AG09319	gingival:	n/a
16	chr14:84903063-84903113	SAEC	small airway:	n/a
17	chr14:85689636-85689686	SKMC	muscle:	n/a
18	chr14:84867542-84867592	HRCEpiC	kidney:	n/a
19	chr14:84965587-84965637	HL-60	blood:	n/a
20	chr14:84978099-84978149	HCM	heart:	n/a
21	chr14:84965587-84965637	GM19239	blood:	n/a
22	chr14:85689636-85689686	SK-N-MC	brain:	n/a
23	chr14:84903063-84903113	HIPEpiC	eye:	n/a
24	chr14:85058259-85058309	SK-N-SH	brain:	n/a
25	chr14:84867542-84867592	MCF10A-Er-Src	breast:	n/a
26	chr14:84867542-84867592	ovcar-3	ovarian:	n/a
27	chr14:84965587-84965637	SK-N-SH_RA	brain:	n/a
28	chr14:84979439-84979489	GM12891	blood:	n/a
29	chr14:84979439-84979489	HCM	heart:	n/a
30	chr14:85074064-85074114	HRPEpiC	eye:	n/a
31	chr14:85292067-85292117	HRE	kidney:	n/a
32	chr14:84867542-84867592	SK-N-SH	brain:	n/a
33	chr14:85292067-85292117	AoSMC	blood vessel:	n/a
34	chr14:84949272-84949322	ovcar-3	ovarian:	n/a
35	chr14:85214861-85214911	SAEC	small airway:	n/a
36	chr14:84978099-84978149	ECC-1	luminal epithelium:	n/a
37	chr14:85010778-85010828	PFSK-1	brain:	n/a
38	chr14:85214861-85214911	GM12891	blood:	n/a
39	chr14:85058259-85058309	GM06990	blood:	n/a
40	chr14:84903063-84903113	ovcar-3	ovarian:	n/a
41	chr14:85214861-85214911	ECC-1	luminal epithelium:	n/a
42	chr14:84965587-84965637	LNCaP	prostate:	n/a
43	chr14:84979439-84979489	HepG2	liver:	n/a
44	chr14:85074064-85074114	HRE	kidney:	n/a
45	chr14:84965587-84965637	PANC-1	pancreas:	n/a
46	chr14:85689636-85689686	AG10803	skin:	n/a
47	chr14:85667733-85667783	HAEpiC	amniotic membrane:	n/a
48	chr14:85667733-85667783	HPAEpiC	pulmonary alveolar:	n/a
49	chr14:85058259-85058309	AoSMC	blood vessel:	n/a
50	chr14:85689636-85689686	PrEC	prostate:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:85097559..85099789-chr14:85925744..85927623,2	K562	blood:
2	chr14:85245111..85246756-chr14:85275178..85277900,2	K562	blood:
3	chr14:83766559..83767404-chr14:85597812..85598521,2	MCF-7	breast:
4	chr14:85009477..85011974-chr14:85012682..85014738,2	K562	blood:
5	chr14:85490593..85492977-chr14:85499997..85502268,2	K562	blood:
6	chr14:84941421..84943706-chr14:84949512..84951375,2	MCF-7	breast:
7	chr14:84972764..84974846-chr7:129843763..129846483,2	MCF-7	breast:
8	chr14:85563318..85564867-chr14:85565112..85566756,2	MCF-7	breast:
9	chr14:84941421..84943706-chr14:84949512..84951375,2	MCF-7	breast:
10	chr14:85016633..85019613-chr17:41466206..41467718,2	MCF-7	breast:
11	chr14:85276415..85277177-chr14:85295527..85296295,2	MCF-7	breast:
12	chr14:85504367..85505311-chr9:111430924..111431510,2	MCF-7	breast:
13	chr14:85016633..85018133-chr17:41400658..41402667,2	K562	blood:
14	chr14:85276415..85277177-chr14:85295527..85296295,2	MCF-7	breast:
15	chr14:85490593..85492977-chr14:85499997..85502268,2	K562	blood:
16	chr11:62607627..62609150-chr14:85611227..85612747,2	K562	blood:
17	chr14:85009477..85011974-chr14:85012682..85014738,2	K562	blood:
18	chr14:85245111..85246756-chr14:85275178..85277900,2	K562	blood:
19	chr14:85563318..85564867-chr14:85565112..85566756,2	MCF-7	breast:
20	chr13:112308570..112309331-chr14:85196106..85196606,2	MCF-7	breast:
21	chr14:85611226..85611727-chr17:41463821..41464360,2	HCT-116	colon:
22	chr14:85609727..85612747-chr17:41464783..41468587,4	K562	blood:
23	chr14:84936711..84937231-chr5:5423746..5424427,2	Hela-S3	cervix:
24	chr14:85611227..85612747-chr17:41464225..41466390,2	K562	blood:
25	chr14:85016633..85018133-chr17:41400785..41402667,2	K562	blood:
26	chr14:84876329..84877076-chr17:8942754..8943503,2	MCF-7	breast:
27	chr14:84843657..84844191-chr5:72572440..72573200,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GALC-10	chr14:85701133-85701270	ENSG00000259044
2	lnc-RP11-497E19.2.1-6	chr14:85606972-85607064	l_1023_chr14:85606971-85664205_whiteBloodCell
3	lnc-SEL1L-16	chr14:85060818-85061893	l_1022_chr14:85060817-85065957_brain
4	lnc-SEL1L-15	chr14:84955785-84956179	l_1021_chr14:84943999-84956179_testes
5	lnc-RP11-497E19.2.1-7	chr14:84955781-84956179	l_1020_chr14:84929954-84944137_testes
6	lnc-RP11-497E19.2.1-7	chr14:84944000-84944137	l_1020_chr14:84929954-84944137_testes
7	lnc-GALC-10	chr14:85669193-85669576	ENSG00000259044
8	lnc-RP11-497E19.2.1-6	chr14:85664047-85664205	l_1023_chr14:85606971-85664205_whiteBloodCell
9	lnc-SEL1L-16	chr14:85064714-85065144	l_1022_chr14:85060817-85065957_brain
10	lnc-SEL1L-16	chr14:85065152-85065957	l_1022_chr14:85060817-85065957_brain
11	lnc-RP11-497E19.2.1-7	chr14:84929955-84930056	l_1020_chr14:84929954-84944137_testes
12	lnc-SEL1L-15	chr14:84944000-84944137	l_1021_chr14:84943999-84956179_testes
13	lnc-GALC-15	chr14:85464622-85465640	NONHSAT038108

No data

Variant related genes	Relation type
ENSG00000258506	TF binding region
RNU6-976P	TF binding region
ENSG00000271712	TF binding region
ENSG00000258506	CpG island
RNU6-976P	CpG island
ENSG00000271712	CpG island
ENSG00000146842	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 17612 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:17612 , 50 per page) page: 1 2 3 4 5 6 7 ... 353

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529255451	chr14:84817606-84817607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs182598183	chr14:84817634-84817635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576038732	chr14:84817649-84817650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78005210	chr14:84817690-84817691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187249919	chr14:84817705-84817706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76387110	chr14:84817736-84817737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs55682233	chr14:84817742-84817743	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs527981260	chr14:84817753-84817754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549613508	chr14:84817771-84817772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567166344	chr14:84817772-84817773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs151099736	chr14:84817799-84817800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142555629	chr14:84817835-84817836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs117834200	chr14:84817860-84817861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191288743	chr14:84817913-84817914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554003870	chr14:84817981-84817982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538750115	chr14:84818024-84818025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs373423308	chr14:84818069-84818070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572155998	chr14:84818094-84818095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs542564874	chr14:84818115-84818116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184508364	chr14:84818143-84818144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146501754	chr14:84818145-84818146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs117127292	chr14:84818149-84818150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147903761	chr14:84818159-84818160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533249123	chr14:84818163-84818164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545054972	chr14:84818184-84818185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149766137	chr14:84826905-84826906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183784593	chr14:84826942-84826943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546832153	chr14:84826983-84826984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559799475	chr14:84827016-84827017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530095738	chr14:84827035-84827036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs548735302	chr14:84827061-84827062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570154525	chr14:84827070-84827071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537696700	chr14:84827083-84827084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs146797679	chr14:84827088-84827089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542106772	chr14:84827136-84827137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200168066	chr14:84827142-84827143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs61984206	chr14:84827167-84827168	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs553225372	chr14:84827168-84827169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs572357616	chr14:84827211-84827212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574120887	chr14:84827282-84827283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs201076404	chr14:84827319-84827320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs72705285	chr14:84827323-84827324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556676115	chr14:84827419-84827420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575244226	chr14:84827445-84827446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs367619918	chr14:84827446-84827447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12432589	chr14:84827447-84827448	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs530060121	chr14:84827452-84827453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550344598	chr14:84827474-84827475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548463578	chr14:84827501-84827502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375074297	chr14:84827509-84827510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21569311	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1270 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84817600-84818200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr14:84826800-84827400	Enhancers	Stomach Mucosa	stomach
3	chr14:84827400-84827800	Weak transcription	Stomach Mucosa	stomach
4	chr14:84827800-84828200	Enhancers	Stomach Mucosa	stomach
5	chr14:84837000-84837400	Enhancers	Brain Germinal Matrix	brain
6	chr14:84838800-84841200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr14:84839000-84843600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr14:84841200-84842200	Enhancers	HUVEC	blood vessel
9	chr14:84841200-84842400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr14:84841400-84842200	Enhancers	NH-A	brain
11	chr14:84841600-84842200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr14:84841600-84842200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr14:84841600-84842200	Enhancers	HSMMtube	muscle
14	chr14:84842200-84843200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr14:84842200-84845600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr14:84842400-84843400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr14:84843200-84844800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr14:84843400-84843800	Enhancers	NHEK	skin
19	chr14:84843600-84843800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr14:84843600-84843800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr14:84845600-84846000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr14:84845600-84846000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr14:84845600-84846200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr14:84845800-84846200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr14:84856200-84856400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr14:84856200-84856600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr14:84856400-84856800	Enhancers	Fetal Lung	lung
28	chr14:84856400-84864400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr14:84864000-84864400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr14:84864400-84864600	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
31	chr14:84864400-84864800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr14:84864600-84864800	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
33	chr14:84865000-84876000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr14:84867200-84867600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr14:84867600-84868000	Enhancers	Fetal Lung	lung
36	chr14:84867600-84869800	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr14:84867800-84868200	Enhancers	Fetal Heart	heart
38	chr14:84868200-84869800	Weak transcription	Fetal Heart	heart
39	chr14:84869800-84870200	Enhancers	Fetal Heart	heart
40	chr14:84869800-84870800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr14:84869800-84871000	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr14:84870000-84870400	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr14:84870000-84870800	Enhancers	H1 Cell Line	embryonic stem cell
44	chr14:84870000-84870800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr14:84870000-84871400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr14:84870000-84871400	Enhancers	Fetal Kidney	kidney
47	chr14:84870200-84870600	Enhancers	Placenta Amnion	Placenta Amnion
48	chr14:84870400-84875600	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr14:84870800-84871600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr14:84870800-84876200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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