Variant report

Variant	esv1841470
Chromosome Location	chr14:67140676-67335425
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	chr14:67213116-67213393	K562	blood:	n/a	n/a
2	ARID3A	chr14:67224984-67225061	HepG2	liver:	n/a	n/a
3	ATF2	chr14:67218740-67219290	GM12878	blood:	n/a	n/a
4	ATF2	chr14:67218758-67219207	GM12878	blood:	n/a	n/a
5	BACH1	chr14:67305949-67305970	K562	blood:	n/a	n/a
6	BATF	chr14:67218778-67219263	GM12878	blood:	n/a	n/a
7	BATF	chr14:67218719-67219305	GM12878	blood:	n/a	n/a
8	BCL11A	chr14:67218813-67219271	GM12878	blood:	n/a	n/a
9	BCL11A	chr14:67219021-67219287	GM12878	blood:	n/a	n/a
10	BHLHE40	chr14:67218905-67219220	GM12878	blood:	n/a	n/a
11	BRCA1	chr14:67288110-67288222	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr14:67202769-67202812	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr14:67198693-67198850	K562	blood:	n/a	n/a
14	CEBPB	chr14:67310889-67310923	A549	lung:	n/a	n/a
15	CEBPB	chr14:67280306-67280665	H1-hESC	embryonic stem cell:	n/a	chr14:67280486-67280497
16	CEBPB	chr14:67237118-67237434	Hela-S3	cervix:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
17	CEBPB	chr14:67280292-67280682	HepG2	liver:	n/a	chr14:67280486-67280497
18	CEBPB	chr14:67280261-67280604	HepG2	liver:	n/a	chr14:67280486-67280497
19	CEBPB	chr14:67280360-67280549	HepG2	liver:	n/a	chr14:67280486-67280497
20	CEBPB	chr14:67164729-67164837	HepG2	liver:	n/a	chr14:67164778-67164789 chr14:67164779-67164790
21	CEBPB	chr14:67280308-67280682	HepG2	liver:	n/a	chr14:67280486-67280497
22	CEBPB	chr14:67326052-67326430	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:67175064-67175343	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:67280182-67280792	A549	lung:	n/a	chr14:67280486-67280497
25	CEBPB	chr14:67280318-67280671	ECC-1	luminal epithelium:	n/a	chr14:67280486-67280497
26	CEBPB	chr14:67326093-67326355	A549	lung:	n/a	n/a
27	CEBPB	chr14:67325909-67326408	HepG2	liver:	n/a	n/a
28	CEBPB	chr14:67237108-67237444	HepG2	liver:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
29	CEBPB	chr14:67280307-67280679	Hela-S3	cervix:	n/a	chr14:67280486-67280497
30	CEBPB	chr14:67326212-67326326	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr14:67290364-67290658	IMR90	lung:	n/a	n/a
32	CEBPB	chr14:67250490-67250759	HepG2	liver:	n/a	n/a
33	CEBPB	chr14:67280301-67280681	K562	blood:	n/a	chr14:67280486-67280497
34	CEBPB	chr14:67280194-67280806	MCF-7	breast:	n/a	chr14:67280486-67280497
35	CEBPB	chr14:67280297-67280677	A549	lung:	n/a	chr14:67280486-67280497
36	CEBPB	chr14:67326120-67326325	HepG2	liver:	n/a	n/a
37	CEBPB	chr14:67237139-67237466	IMR90	lung:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
38	CEBPB	chr14:67237135-67237372	H1-hESC	embryonic stem cell:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
39	CEBPB	chr14:67176141-67176415	IMR90	lung:	n/a	n/a
40	CEBPB	chr14:67176164-67176408	A549	lung:	n/a	n/a
41	CEBPB	chr14:67280274-67280662	A549	lung:	n/a	chr14:67280486-67280497
42	CEBPB	chr14:67176094-67176421	HCT-116	colon:	n/a	n/a
43	CEBPB	chr14:67176089-67176439	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr14:67237138-67237439	A549	lung:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
45	CEBPB	chr14:67326090-67326343	HepG2	liver:	n/a	n/a
46	CEBPB	chr14:67290366-67290605	A549	lung:	n/a	n/a
47	CEBPB	chr14:67280291-67280680	ECC-1	luminal epithelium:	n/a	chr14:67280486-67280497
48	CEBPB	chr14:67280214-67280811	MCF-7	breast:	n/a	chr14:67280486-67280497
49	CEBPB	chr14:67250483-67250759	A549	lung:	n/a	n/a
50	CEBPB	chr14:67237101-67237436	K562	blood:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:67292488-67292538	SK-N-SH	brain:	n/a
2	chr14:67292488-67292538	SK-N-SH	brain:	n/a
3	chr14:67292488-67292538	AoSMC	blood vessel:	n/a
4	chr14:67292488-67292538	HCPEpiC	choroid plexus:	n/a
5	chr14:67292488-67292538	Hela-S3	cervix:	n/a
6	chr14:67292488-67292538	HRCEpiC	kidney:	n/a
7	chr14:67292488-67292538	GM06990	blood:	n/a
8	chr14:67292488-67292538	AG04450	lung:	fetal
9	chr14:67292488-67292538	HIPEpiC	eye:	n/a
10	chr14:67292488-67292538	RPTEC	kidney:	n/a
11	chr14:67292488-67292538	HMEC	breast:	n/a
12	chr14:67292488-67292538	BE2_C	brain:	n/a
13	chr14:67292488-67292538	HAEpiC	amniotic membrane:	n/a
14	chr14:67292488-67292538	NHBE	bronchial:	n/a
15	chr14:67292488-67292538	MCF10A-Er-Src	breast:	n/a
16	chr14:67292488-67292538	MCF-7	breast:	n/a
17	chr14:67292488-67292538	BJ	skin:	n/a
18	chr14:67292488-67292538	AG09309	skin:	n/a
19	chr14:67292488-67292538	SKMC	muscle:	n/a
20	chr14:67292488-67292538	AG04449	skin:	fetal
21	chr14:67292488-67292538	HEEpiC	esophagus:	n/a
22	chr14:67292488-67292538	ProgFib	skin:	n/a
23	chr14:67292488-67292538	GM19239	blood:	n/a
24	chr14:67292488-67292538	HL-60	blood:	n/a
25	chr14:67292488-67292538	AG10803	skin:	n/a
26	chr14:67292488-67292538	H1-hESC	embryonic stem cell:	embryo
27	chr14:67292488-67292538	HRPEpiC	eye:	n/a
28	chr14:67292488-67292538	ovcar-3	ovarian:	n/a
29	chr14:67292488-67292538	HEK293	kidney:	embryo
30	chr14:67292488-67292538	HUVEC	blood vessel:	n/a
31	chr14:67292488-67292538	PrEC	prostate:	n/a
32	chr14:67292488-67292538	CMK	blood:	n/a
33	chr14:67292488-67292538	Jurkat	blood:	n/a
34	chr14:67292488-67292538	PFSK-1	brain:	n/a
35	chr14:67292488-67292538	PANC-1	pancreas:	n/a
36	chr14:67292488-67292538	SK-N-MC	brain:	n/a
37	chr14:67292488-67292538	GM12878	blood:	n/a
38	chr14:67292488-67292538	A549	lung:	n/a
39	chr14:67292488-67292538	HepG2	liver:	n/a
40	chr14:67292488-67292538	ECC-1	luminal epithelium:	n/a
41	chr14:67292488-67292538	LNCaP	prostate:	n/a
42	chr14:67292488-67292538	SAEC	small airway:	n/a
43	chr14:67292488-67292538	HCF	heart:	n/a
44	chr14:67292488-67292538	IMR90	lung:	fetal
45	chr14:67292488-67292538	NB4	blood:	n/a
46	chr14:67292488-67292538	HRE	kidney:	n/a
47	chr14:67292488-67292538	HCT-116	colon:	n/a
48	chr14:67292488-67292538	HPAEpiC	pulmonary alveolar:	n/a
49	chr14:67292488-67292538	Caco-2	colon:	n/a
50	chr14:67292488-67292538	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:67154703..67157341-chr14:67158405..67161202,2	MCF-7	breast:
2	chr14:67145360..67148245-chr14:67155765..67157650,2	MCF-7	breast:
3	chr14:67292902..67294544-chr14:67295956..67298374,2	MCF-7	breast:
4	chr14:67297492..67297992-chr6:10786994..10787529,2	MCF-7	breast:
5	chr14:67310130..67311981-chr14:67312589..67315388,2	MCF-7	breast:
6	chr14:67221145..67223857-chr14:67240535..67242119,2	K562	blood:
7	chr14:67247462..67249948-chr14:67251250..67254048,2	MCF-7	breast:
8	chr14:66868171..66869202-chr14:67212732..67213746,3	MCF-7	breast:
9	chr14:67273370..67275073-chr14:67291638..67294473,2	K562	blood:
10	chr14:67221145..67223857-chr14:67240535..67242119,2	K562	blood:
11	chr14:67249480..67250181-chr17:59494053..59494794,2	MCF-7	breast:
12	chr14:67247462..67249948-chr14:67251250..67254048,2	MCF-7	breast:
13	chr14:67292902..67294544-chr14:67295956..67298374,2	MCF-7	breast:
14	chr14:67154703..67157341-chr14:67158405..67161202,2	MCF-7	breast:
15	chr14:67273370..67275073-chr14:67291638..67294473,2	K562	blood:
16	chr14:67145360..67148245-chr14:67155765..67157650,2	MCF-7	breast:
17	chr14:67290864..67292814-chr14:67296432..67298009,2	MCF-7	breast:
18	chr14:66974629..66976267-chr14:67206447..67208432,2	MCF-7	breast:
19	chr14:67091099..67091710-chr14:67212729..67213799,3	MCF-7	breast:
20	chr14:67310130..67311981-chr14:67312589..67315388,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM71D-3	chr14:67227250-67227736	NONHSAT037427
2	lnc-ATP6V1D-5	chr14:67187470-67188083	predAs_ge08_ARG2_2
3	lnc-ATP6V1D-6	chr14:67184597-67184862	expRegAs_chr14_4324_-

Variant related genes	Relation type
GPHN	TF binding region
ENSG00000258796	TF binding region
GPHN	CpG island
ENSG00000258796	CpG island
ENSG00000171723	chromatin interactions
ENSG00000258561	chromatin interactions

Extended variants
information (count: 7054 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:7054 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10139822	chr14:67140676-67140677	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536650768	chr14:67140691-67140692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189601288	chr14:67140719-67140720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371634957	chr14:67140751-67140752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112030076	chr14:67140807-67140808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370219778	chr14:67140821-67140822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs61117015	chr14:67140834-67140835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368050192	chr14:67140880-67140881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576300186	chr14:67140886-67140887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183948501	chr14:67140910-67140911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188899803	chr14:67140912-67140913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145867073	chr14:67140951-67140952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs28791200	chr14:67140954-67140955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138424834	chr14:67140984-67140985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560653016	chr14:67141086-67141087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560733992	chr14:67141089-67141090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529728986	chr14:67141185-67141186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549767419	chr14:67141210-67141211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192911530	chr14:67141223-67141224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547792496	chr14:67141224-67141225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528158193	chr14:67141251-67141252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76977308	chr14:67141274-67141275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552097358	chr14:67141285-67141286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568016014	chr14:67141359-67141360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534398769	chr14:67141361-67141362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75949831	chr14:67141376-67141377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183676258	chr14:67141399-67141400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs9671762	chr14:67141406-67141407	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs556553957	chr14:67141432-67141433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576335821	chr14:67141512-67141513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141327162	chr14:67141544-67141545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187326111	chr14:67141545-67141546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533675472	chr14:67141552-67141553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571963566	chr14:67141632-67141633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150230695	chr14:67141644-67141645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560718103	chr14:67141680-67141681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574512306	chr14:67141681-67141682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543131624	chr14:67141690-67141691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547448666	chr14:67141693-67141694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532000108	chr14:67141706-67141707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs9671772	chr14:67141707-67141708	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs565577048	chr14:67141711-67141712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527959047	chr14:67141717-67141718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548024693	chr14:67141728-67141729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567743021	chr14:67141733-67141734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369472973	chr14:67141738-67141739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536779483	chr14:67141776-67141777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138794181	chr14:67141794-67141795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570095072	chr14:67141807-67141808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538650372	chr14:67141850-67141851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Acute myeloid leukemia	21251322	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Autism	22495309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21611746	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:529 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67139800-67145400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr14:67144400-67168200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr14:67144600-67145800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
4	chr14:67145400-67145800	ZNF genes & repeats	Fetal Lung	lung
5	chr14:67145400-67145800	ZNF genes & repeats	Ovary	ovary
6	chr14:67145400-67146000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
7	chr14:67145400-67146000	ZNF genes & repeats	Aorta	Aorta
8	chr14:67145400-67146000	ZNF genes & repeats	Liver	Liver
9	chr14:67145400-67146400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr14:67145600-67145800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr14:67145600-67146000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
12	chr14:67146000-67156600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr14:67146000-67172000	Weak transcription	Liver	Liver
14	chr14:67146400-67148400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr14:67146600-67149000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr14:67146800-67148400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr14:67147400-67151000	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr14:67148000-67162000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr14:67148200-67151000	Weak transcription	Dnd41	blood
20	chr14:67148400-67148800	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr14:67148400-67149000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr14:67148800-67169400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr14:67149000-67156200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr14:67151000-67151400	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
25	chr14:67151000-67151400	ZNF genes & repeats	Dnd41	blood
26	chr14:67151400-67151600	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr14:67154200-67164200	Weak transcription	Primary hematopoietic stem cells	blood
28	chr14:67154600-67154800	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr14:67157400-67157800	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr14:67157600-67158200	Enhancers	Gastric	stomach
31	chr14:67157600-67174800	Weak transcription	HepG2	liver
32	chr14:67158000-67158200	Enhancers	Lung	lung
33	chr14:67162000-67163200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr14:67166600-67168200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr14:67166600-67170600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr14:67167800-67168200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr14:67168000-67168400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr14:67168200-67168400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr14:67168200-67168400	ZNF genes & repeats	Esophagus	oesophagus
40	chr14:67168200-67168600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr14:67168200-67168600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr14:67168200-67168600	Enhancers	NHEK	skin
43	chr14:67168200-67168800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr14:67168200-67168800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr14:67168200-67168800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr14:67168200-67168800	ZNF genes & repeats	Fetal Intestine Small	intestine
47	chr14:67168200-67168800	ZNF genes & repeats	Lung	lung
48	chr14:67168200-67169000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr14:67168200-67169000	Enhancers	HMEC	breast
50	chr14:67168400-67168600	Enhancers	Esophagus	oesophagus

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