Variant report

Variant	esv1830605
Chromosome Location	chr14:105268228-105277209
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:34)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105217632..105222660-chr14:105263642..105269157,6	K562	blood:
2	chr14:105267362..105269092-chr14:105436440..105438681,2	MCF-7	breast:
3	chr14:105275614..105278023-chr17:32632159..32633680,2	MCF-7	breast:
4	chr14:105265450..105268632-chr14:105270321..105274809,6	K562	blood:
5	chr14:105269496..105271727-chr14:105330023..105331660,2	MCF-7	breast:
6	chr14:105271769..105274271-chr14:105354431..105356106,2	MCF-7	breast:
7	chr14:105217744..105223022-chr14:105270207..105275140,8	MCF-7	breast:
8	chr14:105265912..105268902-chr14:105329301..105333250,7	MCF-7	breast:
9	chr14:105270335..105272175-chr14:105398279..105400751,2	K562	blood:
10	chr14:105265825..105268360-chr14:105330933..105332611,2	K562	blood:
11	chr14:105272099..105273937-chr14:105275097..105277175,2	K562	blood:
12	chr14:105271965..105273558-chr6:154674183..154677149,2	MCF-7	breast:
13	chr14:105217901..105222027-chr14:105264438..105269623,6	K562	blood:
14	chr14:105269764..105273524-chr14:105273712..105277284,3	K562	blood:
15	chr14:105269532..105276799-chr14:105278912..105285805,20	K562	blood:
16	chr14:105269866..105272402-chr8:125485710..125488000,2	MCF-7	breast:
17	chr14:105216947..105220630-chr14:105265563..105270028,6	MCF-7	breast:
18	chr14:105201310..105203058-chr14:105268966..105270769,2	MCF-7	breast:
19	chr14:105267306..105268128-chr14:105276242..105277034,2	MCF-7	breast:
20	chr14:105155908..105158880-chr14:105275037..105277471,2	MCF-7	breast:
21	chr14:104583312..104585180-chr14:105266957..105269171,2	MCF-7	breast:
22	chr14:105175368..105177558-chr14:105266041..105268999,2	MCF-7	breast:
23	chr14:105189943..105192068-chr14:105271473..105274094,2	MCF-7	breast:
24	chr14:105259095..105269353-chr14:105280422..105289302,26	K562	blood:
25	chr14:105271797..105274173-chr16:57601210..57604193,2	MCF-7	breast:
26	chr14:105269764..105273524-chr14:105273712..105277284,3	K562	blood:
27	chr14:105268465..105270651-chr14:105635461..105637238,2	K562	blood:
28	chr14:105276873..105279342-chr14:105282954..105284515,2	K562	blood:
29	chr14:105268427..105271161-chr14:105291567..105294333,2	K562	blood:
30	chr14:105272219..105273865-chr9:134838230..134839731,2	MCF-7	breast:
31	chr14:105188315..105194275-chr14:105263600..105268559,9	MCF-7	breast:
32	chr14:105272099..105273937-chr14:105275097..105277175,2	K562	blood:
33	chr14:105266268..105268334-chr14:105486957..105488737,2	K562	blood:
34	chr14:105272275..105274283-chr14:105332253..105335339,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000245149	chromatin interactions
ENSG00000207568	chromatin interactions
ENSG00000184990	chromatin interactions
ENSG00000203485	chromatin interactions
ENSG00000166428	chromatin interactions
ENSG00000185100	chromatin interactions
ENSG00000185567	chromatin interactions
ENSG00000179627	chromatin interactions
ENSG00000170779	chromatin interactions
ENSG00000258858	chromatin interactions
ENSG00000170881	chromatin interactions
ENSG00000258701	chromatin interactions
ENSG00000099814	chromatin interactions

Extended variants
information (count: 411 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:411 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4983387	chr14:105268228-105268229	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559429910	chr14:105268350-105268351	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs147665201	chr14:105268392-105268393	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs369088396	chr14:105268410-105268411	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs145420561	chr14:105268413-105268414	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs548060713	chr14:105268424-105268425	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs571182435	chr14:105268428-105268429	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs533530517	chr14:105268436-105268437	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs550382372	chr14:105268449-105268450	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs570029118	chr14:105268487-105268488	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs535992574	chr14:105268500-105268501	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs73350336	chr14:105268511-105268512	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs565696850	chr14:105268515-105268516	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs534701103	chr14:105268538-105268539	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs142321750	chr14:105268544-105268545	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs563442607	chr14:105268545-105268546	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs373878359	chr14:105268569-105268570	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs375499035	chr14:105268595-105268596	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs577534064	chr14:105268622-105268623	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs529115498	chr14:105268661-105268662	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs61734768	chr14:105268701-105268702	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs557164398	chr14:105268723-105268724	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs573642664	chr14:105268727-105268728	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs145613562	chr14:105268740-105268741	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs559491274	chr14:105268743-105268744	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs114717666	chr14:105268758-105268759	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs545037207	chr14:105268759-105268760	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs4145854	chr14:105268768-105268769	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs148885604	chr14:105268782-105268783	Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs373056692	chr14:105268811-105268812	Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs562214833	chr14:105268821-105268822	Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs550104413	chr14:105268836-105268837	Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs563949277	chr14:105268850-105268851	Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs183587440	chr14:105268925-105268926	Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs549019899	chr14:105268949-105268950	Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs370702203	chr14:105268953-105268954	Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs534668840	chr14:105268974-105268975	Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs372776172	chr14:105268975-105268976	Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs188963600	chr14:105268990-105268991	Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs115636909	chr14:105269024-105269025	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs143538688	chr14:105269029-105269030	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs556982474	chr14:105269039-105269040	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs573731119	chr14:105269060-105269061	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs536077564	chr14:105269131-105269132	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs558566527	chr14:105269150-105269151	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs527828832	chr14:105269174-105269175	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs543691621	chr14:105269269-105269270	Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs573008867	chr14:105269288-105269289	Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs544998580	chr14:105269299-105269300	Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs564919643	chr14:105269325-105269326	Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
Lung cancer	18438408	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
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:363 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105267200-105268400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr14:105267200-105268600	Bivalent Enhancer	Fetal Brain Male	brain
3	chr14:105267400-105268400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr14:105267400-105268400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr14:105267400-105268400	Flanking Active TSS	Liver	Liver
6	chr14:105267400-105268400	Flanking Active TSS	Right Ventricle	heart
7	chr14:105267400-105268400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
8	chr14:105267400-105268400	Flanking Active TSS	Dnd41	blood
9	chr14:105267400-105268600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr14:105267400-105268600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr14:105267400-105268600	Flanking Active TSS	Colonic Mucosa	Colon
12	chr14:105267400-105270000	Flanking Active TSS	Stomach Smooth Muscle	stomach
13	chr14:105267600-105268400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
14	chr14:105267600-105268400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr14:105267600-105268400	Flanking Active TSS	Rectal Smooth Muscle	rectum
16	chr14:105267600-105268400	Flanking Bivalent TSS/Enh	Thymus	Thymus
17	chr14:105267600-105268400	Flanking Active TSS	Hela-S3	cervix
18	chr14:105267600-105268400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
19	chr14:105267600-105268600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
20	chr14:105267600-105268600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
21	chr14:105267600-105268600	Flanking Active TSS	Gastric	stomach
22	chr14:105267800-105268400	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr14:105267800-105268400	Flanking Active TSS	Colon Smooth Muscle	Colon
24	chr14:105267800-105268400	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
25	chr14:105267800-105268400	Enhancers	Placenta Amnion	Placenta Amnion
26	chr14:105267800-105268400	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr14:105267800-105268400	Flanking Active TSS	GM12878-XiMat	blood
28	chr14:105267800-105268400	Flanking Active TSS	NHEK	skin
29	chr14:105267800-105268600	Genic enhancers	Spleen	Spleen
30	chr14:105267800-105268600	Flanking Active TSS	HepG2	liver
31	chr14:105267800-105268800	Flanking Active TSS	Primary T cells from cord blood	blood
32	chr14:105268000-105268400	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr14:105268000-105268400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
34	chr14:105268000-105268400	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
35	chr14:105268000-105268400	Enhancers	Brain Cingulate Gyrus	brain
36	chr14:105268000-105268400	Enhancers	Brain Hippocampus Middle	brain
37	chr14:105268000-105268400	Bivalent Enhancer	Fetal Brain Female	brain
38	chr14:105268000-105268400	Enhancers	Lung	lung
39	chr14:105268000-105268400	Enhancers	Right Atrium	heart
40	chr14:105268000-105268400	Enhancers	HUVEC	blood vessel
41	chr14:105268000-105268400	Enhancers	K562	blood
42	chr14:105268000-105268400	Bivalent Enhancer	Osteobl	bone
43	chr14:105268000-105268600	Genic enhancers	Cortex derived primary cultured neurospheres	brain
44	chr14:105268000-105268600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr14:105268000-105268600	Bivalent Enhancer	Fetal Thymus	thymus
46	chr14:105268000-105268800	Transcr. at gene 5' and 3'	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr14:105268000-105268800	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr14:105268000-105268800	Genic enhancers	Esophagus	oesophagus
49	chr14:105268000-105268800	Enhancers	Ovary	ovary
50	chr14:105268000-105269000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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