Variant report

Variant	nsv1042258
Chromosome Location	chr14:46336392-46453750
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:426)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:46337595-46337969	GM12878	blood:	n/a	n/a
2	ATF2	chr14:46375372-46375853	GM12878	blood:	n/a	n/a
3	ATF2	chr14:46337571-46338159	GM12878	blood:	n/a	n/a
4	ATF2	chr14:46336378-46337127	GM12878	blood:	n/a	n/a
5	BACH1	chr14:46351093-46351107	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr14:46337483-46337971	GM12878	blood:	n/a	chr14:46337729-46337740
7	BATF	chr14:46375489-46375749	GM12878	blood:	n/a	n/a
8	BATF	chr14:46368023-46368235	GM12878	blood:	n/a	n/a
9	BATF	chr14:46337483-46338059	GM12878	blood:	n/a	chr14:46337729-46337740
10	BATF	chr14:46375483-46375752	GM12878	blood:	n/a	n/a
11	BATF	chr14:46336397-46337076	GM12878	blood:	n/a	n/a
12	BCL11A	chr14:46338183-46338481	GM12878	blood:	n/a	n/a
13	BCL11A	chr14:46337580-46337867	GM12878	blood:	n/a	n/a
14	BCL11A	chr14:46337474-46337979	GM12878	blood:	n/a	n/a
15	BCL11A	chr14:46375429-46375807	GM12878	blood:	n/a	n/a
16	BCL3	chr14:46337522-46337975	GM12878	blood:	n/a	n/a
17	BCL3	chr14:46337578-46337949	GM12878	blood:	n/a	n/a
18	BCL3	chr14:46336621-46336979	GM12878	blood:	n/a	n/a
19	BCLAF1	chr14:46337617-46337960	GM12878	blood:	n/a	n/a
20	BHLHE40	chr14:46337665-46337965	GM12878	blood:	n/a	n/a
21	CEBPB	chr14:46388459-46388948	MCF-7	breast:	n/a	chr14:46388709-46388720
22	CEBPB	chr14:46388540-46388897	IMR90	lung:	n/a	chr14:46388709-46388720
23	CEBPB	chr14:46441175-46441403	HepG2	liver:	n/a	chr14:46441316-46441327
24	CEBPB	chr14:46388540-46388874	HepG2	liver:	n/a	chr14:46388709-46388720
25	CEBPB	chr14:46441158-46441496	A549	lung:	n/a	chr14:46441316-46441327
26	CEBPB	chr14:46388507-46388949	MCF-7	breast:	n/a	chr14:46388709-46388720
27	CEBPB	chr14:46441220-46441420	H1-hESC	embryonic stem cell:	n/a	chr14:46441316-46441327
28	CEBPB	chr14:46357543-46357739	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr14:46388556-46388893	A549	lung:	n/a	chr14:46388709-46388720
30	CHD2	chr14:46360235-46360350	HepG2	liver:	n/a	n/a
31	CREB1	chr14:46337522-46338032	GM12878	blood:	n/a	n/a
32	CTCF	chr14:46445787-46445940	NHEK	skin:	n/a	n/a
33	CTCF	chr14:46409488-46409958	MCF-7	breast:	n/a	n/a
34	CTCF	chr14:46445680-46445830	MCF-7	breast:	n/a	n/a
35	CTCF	chr14:46409740-46409890	RPTEC	kidney:	n/a	n/a
36	CTCF	chr14:46340340-46340490	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr14:46349944-46349981	Fibrobl	skin:	n/a	n/a
38	CTCF	chr14:46450796-46450883	GM13976	blood:	n/a	n/a
39	CTCF	chr14:46340320-46340470	GM12871	blood:	n/a	n/a
40	CTCF	chr14:46409620-46409770	BE2_C	brain:	n/a	n/a
41	CTCF	chr14:46407820-46407856	GM20000	blood:	n/a	n/a
42	CTCF	chr14:46409900-46410050	GM06990	blood:	n/a	n/a
43	CTCF	chr14:46346882-46346926	GM20000	blood:	n/a	n/a
44	CTCF	chr14:46340365-46340414	MCF-7	breast:	n/a	n/a
45	CTCF	chr14:46340340-46340490	GM12864	blood:	n/a	n/a
46	CTCF	chr14:46349860-46350010	HEK293	kidney:	n/a	n/a
47	CTCF	chr14:46340320-46340470	BE2_C	brain:	n/a	n/a
48	CTCF	chr14:46445780-46445930	MCF-7	breast:	n/a	n/a
49	CTCF	chr14:46340360-46340510	GM12865	blood:	n/a	n/a
50	CTCF	chr14:46445820-46445970	HMEC	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46358279-46358329	RPTEC	kidney:	n/a
2	chr14:46358279-46358329	MCF-7	breast:	n/a
3	chr14:46358279-46358329	Jurkat	blood:	n/a
4	chr14:46358139-46358189	T-47D	breast:	n/a
5	chr14:46358139-46358189	HRCEpiC	kidney:	n/a
6	chr14:46358139-46358189	MCF10A-Er-Src	breast:	n/a
7	chr14:46358139-46358189	Caco-2	colon:	n/a
8	chr14:46358139-46358189	SK-N-SH_RA	brain:	n/a
9	chr14:46358279-46358329	HAEpiC	amniotic membrane:	n/a
10	chr14:46358279-46358329	AG04450	lung:	fetal
11	chr14:46358279-46358329	SK-N-SH	brain:	n/a
12	chr14:46358279-46358329	GM19239	blood:	n/a
13	chr14:46358139-46358189	AG04450	lung:	fetal
14	chr14:46358279-46358329	SAEC	small airway:	n/a
15	chr14:46358139-46358189	HIPEpiC	eye:	n/a
16	chr14:46358279-46358329	IMR90	lung:	fetal
17	chr14:46358279-46358329	HRPEpiC	eye:	n/a
18	chr14:46358279-46358329	PFSK-1	brain:	n/a
19	chr14:46358279-46358329	SK-N-MC	brain:	n/a
20	chr14:46358279-46358329	HCM	heart:	n/a
21	chr14:46358139-46358189	BE2_C	brain:	n/a
22	chr14:46358139-46358189	GM19239	blood:	n/a
23	chr14:46358279-46358329	T-47D	breast:	n/a
24	chr14:46358139-46358189	HCM	heart:	n/a
25	chr14:46358279-46358329	HepG2	liver:	n/a
26	chr14:46358139-46358189	HCPEpiC	choroid plexus:	n/a
27	chr14:46358279-46358329	HCF	heart:	n/a
28	chr14:46358279-46358329	PANC-1	pancreas:	n/a
29	chr14:46358279-46358329	SKMC	muscle:	n/a
30	chr14:46358139-46358189	IMR90	lung:	fetal
31	chr14:46358139-46358189	BJ	skin:	n/a
32	chr14:46358139-46358189	NT2-D1	testis:	n/a
33	chr14:46358139-46358189	HL-60	blood:	n/a
34	chr14:46358279-46358329	NH-A	brain:	n/a
35	chr14:46358139-46358189	SAEC	small airway:	n/a
36	chr14:46358279-46358329	HEK293	kidney:	embryo
37	chr14:46358139-46358189	Jurkat	blood:	n/a
38	chr14:46358139-46358189	HMEC	breast:	n/a
39	chr14:46358279-46358329	LNCaP	prostate:	n/a
40	chr14:46358279-46358329	HPAEpiC	pulmonary alveolar:	n/a
41	chr14:46358279-46358329	AoSMC	blood vessel:	n/a
42	chr14:46358139-46358189	HUVEC	blood vessel:	n/a
43	chr14:46358139-46358189	HAEpiC	amniotic membrane:	n/a
44	chr14:46358279-46358329	SK-N-SH_RA	brain:	n/a
45	chr14:46358279-46358329	Hela-S3	cervix:	n/a
46	chr14:46358139-46358189	ProgFib	skin:	n/a
47	chr14:46358139-46358189	AG10803	skin:	n/a
48	chr14:46358279-46358329	BE2_C	brain:	n/a
49	chr14:46358139-46358189	AG09319	gingival:	n/a
50	chr14:46358279-46358329	AG10803	skin:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:122908054..122908892-chr14:46408991..46409734,2	MCF-7	breast:
2	chr14:46385119..46386937-chr14:46388253..46390395,2	MCF-7	breast:
3	chr14:46375125..46377270-chr14:46379726..46383333,3	K562	blood:
4	chr14:46368837..46370409-chr14:46372784..46375382,2	K562	blood:
5	chr14:46308036..46308555-chr14:46409283..46409960,2	MCF-7	breast:
6	chr14:46346207..46348483-chr14:46349392..46352093,2	K562	blood:
7	chr14:46368837..46370409-chr14:46372784..46375382,2	K562	blood:
8	chr14:46385119..46386937-chr14:46388253..46390395,2	MCF-7	breast:
9	chr14:46346207..46348483-chr14:46349392..46352093,2	K562	blood:
10	chr14:46375125..46377270-chr14:46379726..46383333,3	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-9	chr14:46359392-46359577	NONHSAT036675
2	lnc-FANCM-6	chr14:46410146-46410221	ENSG00000258700
3	lnc-FANCM-9	chr14:46376825-46376872	NONHSAT036675

No data

Variant related genes	Relation type
LINC00871	TF binding region
LINC00871	CpG island

Extended variants
information (count: 1466 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372543	chr14:46336392-46336393	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550406445	chr14:46336405-46336406	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs533046928	chr14:46336406-46336407	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs181739197	chr14:46336412-46336413	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs567557983	chr14:46336418-46336419	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs534649393	chr14:46336425-46336426	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs546423140	chr14:46336434-46336435	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs186818490	chr14:46336442-46336443	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs191350076	chr14:46336477-46336478	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs558342137	chr14:46336479-46336480	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs576184757	chr14:46336484-46336485	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs439245	chr14:46336524-46336525	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs376939276	chr14:46336541-46336542	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs562075888	chr14:46336543-46336544	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs143310032	chr14:46336623-46336624	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs148320118	chr14:46336716-46336717	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs141428491	chr14:46336759-46336760	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs147448925	chr14:46336802-46336803	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs113179882	chr14:46336810-46336811	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs374011	chr14:46336819-46336820	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs35084470	chr14:46336836-46336837	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs374049	chr14:46336854-46336855	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs549184728	chr14:46336877-46336878	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs374285484	chr14:46336878-46336879	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs534586419	chr14:46336905-46336906	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs113454358	chr14:46336924-46336925	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs571117962	chr14:46336927-46336928	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs538732848	chr14:46336941-46336942	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs556688301	chr14:46336952-46336953	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs574975771	chr14:46336967-46336968	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs181339133	chr14:46336969-46336970	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs199513973	chr14:46336985-46336986	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs72524391	chr14:46336986-46336987	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs200137038	chr14:46336987-46336988	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs375696094	chr14:46336988-46336989	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs555508176	chr14:46337023-46337024	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs185187630	chr14:46337035-46337036	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs76518403	chr14:46337049-46337050	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs7148763	chr14:46337114-46337115	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs577990265	chr14:46337167-46337168	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs534484260	chr14:46337174-46337175	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs76767942	chr14:46337177-46337178	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs376499568	chr14:46337183-46337184	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs563799791	chr14:46337217-46337218	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs383269	chr14:46337224-46337225	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs574173596	chr14:46337230-46337231	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs189651647	chr14:46337232-46337233	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs182093734	chr14:46337234-46337235	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs7149407	chr14:46337256-46337257	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs374471603	chr14:46337283-46337284	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	19907438	CNVD

Chromatin state (count:157 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46336200-46336400	Active TSS	GM12878-XiMat	blood
2	chr14:46336200-46336800	Enhancers	Fetal Heart	heart
3	chr14:46336200-46338600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr14:46336400-46336600	Flanking Active TSS	GM12878-XiMat	blood
5	chr14:46336600-46337000	Active TSS	GM12878-XiMat	blood
6	chr14:46337000-46337600	Flanking Active TSS	GM12878-XiMat	blood
7	chr14:46337600-46337800	Enhancers	GM12878-XiMat	blood
8	chr14:46337800-46338800	Flanking Active TSS	GM12878-XiMat	blood
9	chr14:46338800-46339000	Enhancers	GM12878-XiMat	blood
10	chr14:46339000-46339200	Weak transcription	GM12878-XiMat	blood
11	chr14:46339200-46339800	ZNF genes & repeats	GM12878-XiMat	blood
12	chr14:46357600-46357800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr14:46357600-46358200	Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr14:46357600-46358200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr14:46357600-46358400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr14:46357600-46358600	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr14:46357600-46358600	Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr14:46357800-46358600	Active TSS	H9 Cell Line	embryonic stem cell
19	chr14:46357800-46358600	Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr14:46358000-46358200	Active TSS	H1 Cell Line	embryonic stem cell
21	chr14:46358000-46358200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr14:46358000-46358600	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr14:46358000-46360800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr14:46358200-46358400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
25	chr14:46358200-46358400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr14:46358200-46358400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr14:46358400-46358600	Active TSS	HUES48 Cell Line	embryonic stem cell
28	chr14:46358400-46358600	Weak transcription	Pancreas	Pancrea
29	chr14:46358400-46360800	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr14:46358400-46360800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr14:46358400-46361000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr14:46358600-46359000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr14:46358600-46359000	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr14:46358600-46360200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr14:46358600-46360400	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr14:46358600-46360400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr14:46358600-46360800	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr14:46359000-46360200	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr14:46359000-46360600	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr14:46359200-46359600	Enhancers	Fetal Kidney	kidney
41	chr14:46359600-46360000	Weak transcription	Fetal Kidney	kidney
42	chr14:46360000-46360600	Enhancers	Fetal Kidney	kidney
43	chr14:46360200-46360600	Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr14:46360200-46360800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr14:46360200-46360800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr14:46360200-46360800	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr14:46360200-46360800	Enhancers	HMEC	breast
48	chr14:46360200-46361400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr14:46360200-46362200	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr14:46360400-46360600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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