Variant report

Variant	esv3328683
Chromosome Location	chr14:105615357-105617555
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6)
CpG islands
(count:366)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EGR1	chr14:105615946-105616154	K562	blood:	n/a	chr14:105616112-105616125
2	ESR1	chr14:105616710-105617013	ECC-1	luminal epithelium:	n/a	chr14:105616912-105616929
3	ESR1	chr14:105616589-105617029	ECC-1	luminal epithelium:	n/a	chr14:105616912-105616929
4	POLR2A	chr14:105615786-105615926	HUVEC	blood vessel:	n/a	n/a
5	ZBTB7A	chr14:105616403-105616831	ECC-1	luminal epithelium:	n/a	n/a
6	ZBTB7A	chr14:105615738-105616105	ECC-1	luminal epithelium:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105617308-105617358	CMK	blood:	n/a
2	chr14:105617173-105617223	HPAEpiC	pulmonary alveolar:	n/a
3	chr14:105617308-105617358	AoSMC	blood vessel:	n/a
4	chr14:105617308-105617358	LNCaP	prostate:	n/a
5	chr14:105617308-105617358	MCF-7	breast:	n/a
6	chr14:105616988-105617038	AG09309	skin:	n/a
7	chr14:105615459-105615509	HRPEpiC	eye:	n/a
8	chr14:105615459-105615509	SK-N-SH	brain:	n/a
9	chr14:105617080-105617130	HCF	heart:	n/a
10	chr14:105617173-105617223	HUVEC	blood vessel:	n/a
11	chr14:105615401-105615451	PFSK-1	brain:	n/a
12	chr14:105617173-105617223	A549	lung:	n/a
13	chr14:105615459-105615509	SKMC	muscle:	n/a
14	chr14:105617173-105617223	Hepatocyte	liver:	n/a
15	chr14:105616988-105617038	SK-N-SH_RA	brain:	n/a
16	chr14:105617173-105617223	Hela-S3	cervix:	n/a
17	chr14:105617080-105617130	BE2_C	brain:	n/a
18	chr14:105615401-105615451	HRPEpiC	eye:	n/a
19	chr14:105617080-105617130	IMR90	lung:	fetal
20	chr14:105615401-105615451	SKMC	muscle:	n/a
21	chr14:105616988-105617038	HepG2	liver:	n/a
22	chr14:105615401-105615451	PANC-1	pancreas:	n/a
23	chr14:105616988-105617038	NT2-D1	testis:	n/a
24	chr14:105617173-105617223	HAEpiC	amniotic membrane:	n/a
25	chr14:105617173-105617223	PrEC	prostate:	n/a
26	chr14:105617308-105617358	GM12891	blood:	n/a
27	chr14:105616988-105617038	A549	lung:	n/a
28	chr14:105617173-105617223	GM12891	blood:	n/a
29	chr14:105615401-105615451	AoSMC	blood vessel:	n/a
30	chr14:105616988-105617038	LNCaP	prostate:	n/a
31	chr14:105616988-105617038	Hela-S3	cervix:	n/a
32	chr14:105617308-105617358	HCF	heart:	n/a
33	chr14:105615459-105615509	HMEC	breast:	n/a
34	chr14:105615459-105615509	IMR90	lung:	fetal
35	chr14:105615459-105615509	AG10803	skin:	n/a
36	chr14:105616988-105617038	HEEpiC	esophagus:	n/a
37	chr14:105616988-105617038	ECC-1	luminal epithelium:	n/a
38	chr14:105616988-105617038	HIPEpiC	eye:	n/a
39	chr14:105615459-105615509	HPAEpiC	pulmonary alveolar:	n/a
40	chr14:105617080-105617130	NH-A	brain:	n/a
41	chr14:105615401-105615451	K562	blood:	n/a
42	chr14:105617080-105617130	Hela-S3	cervix:	n/a
43	chr14:105617173-105617223	MCF10A-Er-Src	breast:	n/a
44	chr14:105617080-105617130	HEK293	kidney:	embryo
45	chr14:105615401-105615451	ProgFib	skin:	n/a
46	chr14:105617080-105617130	Hepatocyte	liver:	n/a
47	chr14:105615459-105615509	GM12878	blood:	n/a
48	chr14:105617173-105617223	K562	blood:	n/a
49	chr14:105616988-105617038	BJ	skin:	n/a
50	chr14:105615459-105615509	HNPCEpiC	eye:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105613142..105616306-chr14:105622290..105625169,3	K562	blood:
2	chr14:105609926..105615692-chr14:105616858..105625128,9	K562	blood:
3	chr14:105191017..105193582-chr14:105615897..105618849,2	MCF-7	breast:
4	chr14:105615698..105618053-chr14:105622347..105625638,3	MCF-7	breast:
5	chr14:105615014..105617239-chr14:105619145..105622136,2	K562	blood:
6	chr14:105609926..105615692-chr14:105616858..105625128,9	K562	blood:
7	chr14:105438558..105440399-chr14:105616229..105618880,2	MCF-7	breast:
8	chr14:105614227..105617896-chr14:105637328..105640796,3	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6765-3p	chr14:105617115-105617135	MIMAT0027431
hsa-miR-6765-5p	chr14:105617177-105617201	MIMAT0027430

No data

Variant related genes	Relation type
JAG2	TF binding region
JAG2	CpG island
ENSG00000184916	chromatin interactions
ENSG00000183828	chromatin interactions

Extended variants
information (count: 121 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:121 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145041298	chr14:105615359-105615360	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs138823032	chr14:105615368-105615369	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs201468009	chr14:105615370-105615371	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs369686885	chr14:105615381-105615382	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs141987287	chr14:105615389-105615390	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs145627661	chr14:105615397-105615398	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs138503062	chr14:105615402-105615403	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs200911938	chr14:105615404-105615405	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs372399094	chr14:105615413-105615414	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs142004780	chr14:105615422-105615423	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs587752292	chr14:105615433-105615434	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs36024978	chr14:105615449-105615450	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs368900540	chr14:105615451-105615452	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs375459787	chr14:105615463-105615464	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs587684260	chr14:105615471-105615472	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs587740355	chr14:105615474-105615475	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs587621733	chr14:105615477-105615478	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs370004206	chr14:105615482-105615483	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs374294516	chr14:105615495-105615496	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs377414264	chr14:105615504-105615505	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs368778866	chr14:105615514-105615515	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs199566648	chr14:105615529-105615530	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs202068896	chr14:105615534-105615535	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs374569282	chr14:105615543-105615544	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs150669646	chr14:105615593-105615594	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs368871084	chr14:105615611-105615612	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs139834065	chr14:105615615-105615616	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs9972231	chr14:105615648-105615649	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs587692038	chr14:105615649-105615650	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs181385226	chr14:105615664-105615665	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs587637403	chr14:105615675-105615676	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs375265020	chr14:105615678-105615679	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs201695814	chr14:105615696-105615697	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs373693762	chr14:105615705-105615706	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs587601994	chr14:105615715-105615716	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs587636118	chr14:105615733-105615734	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs150065796	chr14:105615763-105615764	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs587615094	chr14:105615823-105615824	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs587695083	chr14:105615840-105615841	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs145393197	chr14:105615854-105615855	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs148771502	chr14:105615867-105615868	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs587659509	chr14:105615896-105615897	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs587745527	chr14:105615919-105615920	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs149319748	chr14:105616009-105616010	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs587613158	chr14:105616034-105616035	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs57311278	chr14:105616093-105616094	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs587703980	chr14:105616095-105616096	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs587738803	chr14:105616122-105616123	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs587691753	chr14:105616123-105616124	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs587746422	chr14:105616124-105616125	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
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
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	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
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105602800-105629800	Weak transcription	K562	blood
2	chr14:105606400-105617800	Strong transcription	Skeletal Muscle Female	skeletal muscle
3	chr14:105606800-105618000	Weak transcription	Psoas Muscle	Psoas
4	chr14:105606800-105619600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr14:105606800-105631600	Weak transcription	Hela-S3	cervix
6	chr14:105607000-105615400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr14:105607000-105618200	Strong transcription	Gastric	stomach
8	chr14:105607000-105621600	Weak transcription	Duodenum Mucosa	Duodenum
9	chr14:105607200-105616000	Strong transcription	HMEC	breast
10	chr14:105607200-105619600	Weak transcription	Colonic Mucosa	Colon
11	chr14:105607400-105619200	Strong transcription	Pancreas	Pancrea
12	chr14:105607600-105616000	Strong transcription	Fetal Intestine Small	intestine
13	chr14:105607600-105617600	Strong transcription	Skeletal Muscle Male	skeletal muscle
14	chr14:105607600-105625400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr14:105607600-105632000	Weak transcription	Brain Angular Gyrus	brain
16	chr14:105608000-105618000	Strong transcription	Adipose Nuclei	Adipose
17	chr14:105608200-105616400	Strong transcription	Right Ventricle	heart
18	chr14:105608800-105618400	Strong transcription	Lung	lung
19	chr14:105609400-105631400	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr14:105609600-105618800	Weak transcription	Placenta	Placenta
21	chr14:105609600-105622000	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr14:105610000-105631400	Weak transcription	HUVEC	blood vessel
23	chr14:105610200-105625200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr14:105611200-105615800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
25	chr14:105611800-105616000	Strong transcription	NHEK	skin
26	chr14:105612000-105615800	Strong transcription	Left Ventricle	heart
27	chr14:105612800-105621000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr14:105613400-105623000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr14:105613400-105631400	Weak transcription	Brain Anterior Caudate	brain
30	chr14:105613600-105618400	Weak transcription	HSMMtube	muscle
31	chr14:105613600-105619200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr14:105613600-105631400	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr14:105613800-105615600	Strong transcription	Fetal Muscle Leg	muscle
34	chr14:105613800-105615800	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr14:105613800-105616600	Weak transcription	Brain Germinal Matrix	brain
36	chr14:105613800-105616600	Weak transcription	Fetal Muscle Trunk	muscle
37	chr14:105613800-105631400	Weak transcription	Brain Cingulate Gyrus	brain
38	chr14:105614000-105620200	Weak transcription	Fetal Brain Female	brain
39	chr14:105614000-105621600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr14:105614000-105622000	Weak transcription	Brain Hippocampus Middle	brain
41	chr14:105614200-105615400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr14:105614600-105616000	Genic enhancers	Spleen	Spleen
43	chr14:105614600-105619000	Strong transcription	Fetal Stomach	stomach
44	chr14:105614800-105616800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr14:105615200-105615600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr14:105615200-105616000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr14:105615200-105621600	Weak transcription	Esophagus	oesophagus
48	chr14:105615200-105625600	Weak transcription	A549	lung
49	chr14:105615400-105616200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr14:105615600-105615800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland

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