Variant report

Variant	nsv878108
Chromosome Location	chr3:191175215-191223664
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:360)
CpG islands
(count:245)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:191191432-191192143	K562	blood:	n/a	n/a
2	ARID3A	chr3:191209628-191209646	K562	blood:	n/a	n/a
3	ATF3	chr3:191194161-191194511	K562	blood:	n/a	n/a
4	BACH1	chr3:191191387-191191876	K562	blood:	n/a	n/a
5	BHLHE40	chr3:191217493-191217797	K562	blood:	n/a	n/a
6	BHLHE40	chr3:191191581-191191624	K562	blood:	n/a	n/a
7	CBX3	chr3:191217458-191217812	K562	blood:	n/a	n/a
8	CBX3	chr3:191201840-191202240	K562	blood:	n/a	n/a
9	CCNT2	chr3:191217369-191217837	K562	blood:	n/a	n/a
10	CEBPB	chr3:191191338-191191926	K562	blood:	n/a	n/a
11	CEBPB	chr3:191218711-191219079	K562	blood:	n/a	chr3:191218865-191218876 chr3:191218896-191218907
12	CEBPB	chr3:191218718-191219075	H1-hESC	embryonic stem cell:	n/a	chr3:191218865-191218876 chr3:191218896-191218907
13	CEBPB	chr3:191191372-191191877	K562	blood:	n/a	n/a
14	CEBPB	chr3:191221034-191221300	HepG2	liver:	n/a	chr3:191221178-191221189 chr3:191221177-191221190
15	CEBPB	chr3:191191421-191191601	K562	blood:	n/a	n/a
16	CEBPB	chr3:191202309-191202710	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr3:191188359-191188642	K562	blood:	n/a	n/a
18	CEBPB	chr3:191207415-191207435	K562	blood:	n/a	n/a
19	CEBPB	chr3:191203369-191203725	K562	blood:	n/a	n/a
20	CEBPB	chr3:191191384-191191970	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr3:191218714-191219055	HepG2	liver:	n/a	chr3:191218865-191218876 chr3:191218896-191218907
22	CTCF	chr3:191220500-191220650	HepG2	liver:	n/a	chr3:191220559-191220580
23	CTCF	chr3:191220465-191220673	GM12878	blood:	n/a	chr3:191220559-191220580
24	CTCF	chr3:191220440-191220590	WERI-Rb-1	eye:	n/a	chr3:191220559-191220580
25	CTCF	chr3:191220448-191220691	MCF-7	breast:	n/a	chr3:191220559-191220580
26	CTCF	chr3:191220460-191220610	AoAF	blood vessel:	n/a	chr3:191220559-191220580
27	CTCF	chr3:191220500-191220650	Hela-S3	cervix:	n/a	chr3:191220559-191220580
28	CTCF	chr3:191220500-191220650	GM12864	blood:	n/a	chr3:191220559-191220580
29	CTCF	chr3:191220480-191220630	HRPEpiC	eye:	n/a	chr3:191220559-191220580
30	CTCF	chr3:191220520-191220670	HPAF	blood vessel:	n/a	chr3:191220559-191220580
31	CTCF	chr3:191220342-191220742	HCT-116	colon:	n/a	chr3:191220559-191220580
32	CTCF	chr3:191219280-191219430	K562	blood:	n/a	n/a
33	CTCF	chr3:191220500-191220650	HEEpiC	esophagus:	n/a	chr3:191220559-191220580
34	CTCF	chr3:191220506-191220641	ProgFib	skin:	n/a	chr3:191220559-191220580
35	CTCF	chr3:191220500-191220650	GM12866	blood:	n/a	chr3:191220559-191220580
36	CTCF	chr3:191220520-191220670	HUVEC	blood vessel:	n/a	chr3:191220559-191220580
37	CTCF	chr3:191220500-191220650	GM12878	blood:	n/a	chr3:191220559-191220580
38	CTCF	chr3:191220517-191220605	GM10266	blood:	n/a	chr3:191220559-191220580
39	CTCF	chr3:191217631-191217646	NHEK	skin:	n/a	n/a
40	CTCF	chr3:191220540-191220690	HFF	foreskin:	n/a	chr3:191220559-191220580
41	CTCF	chr3:191220420-191220570	AG04449	skin:	n/a	n/a
42	CTCF	chr3:191220500-191220650	BE2_C	brain:	n/a	chr3:191220559-191220580
43	CTCF	chr3:191220463-191220648	HepG2	liver:	n/a	chr3:191220559-191220580
44	CTCF	chr3:191220500-191220650	GM12865	blood:	n/a	chr3:191220559-191220580
45	CTCF	chr3:191220377-191220741	GM12878	blood:	n/a	chr3:191220559-191220580
46	CTCF	chr3:191220480-191220630	HPAF	blood vessel:	n/a	chr3:191220559-191220580
47	CTCF	chr3:191220440-191220590	GM12875	blood:	n/a	chr3:191220559-191220580
48	CTCF	chr3:191220480-191220630	HCT-116	colon:	n/a	chr3:191220559-191220580
49	CTCF	chr3:191220460-191220610	GM12868	blood:	n/a	chr3:191220559-191220580
50	CTCF	chr3:191217630-191217751	MCF-7	breast:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:191178924-191178974	SKMC	muscle:	n/a
2	chr3:191178924-191178974	SKMC	muscle:	n/a
3	chr3:191178384-191178434	HEEpiC	esophagus:	n/a
4	chr3:191179074-191179124	NT2-D1	testis:	n/a
5	chr3:191179074-191179124	GM06990	blood:	n/a
6	chr3:191178924-191178974	HRCEpiC	kidney:	n/a
7	chr3:191179074-191179124	ECC-1	luminal epithelium:	n/a
8	chr3:191178384-191178434	HAEpiC	amniotic membrane:	n/a
9	chr3:191178384-191178434	NHBE	bronchial:	n/a
10	chr3:191178384-191178434	HCT-116	colon:	n/a
11	chr3:191178814-191178864	Hela-S3	cervix:	n/a
12	chr3:191178814-191178864	HepG2	liver:	n/a
13	chr3:191178814-191178864	SK-N-SH_RA	brain:	n/a
14	chr3:191178814-191178864	HPAEpiC	pulmonary alveolar:	n/a
15	chr3:191179074-191179124	SK-N-MC	brain:	n/a
16	chr3:191178814-191178864	Jurkat	blood:	n/a
17	chr3:191178924-191178974	HCM	heart:	n/a
18	chr3:191179074-191179124	PFSK-1	brain:	n/a
19	chr3:191179074-191179124	HCT-116	colon:	n/a
20	chr3:191178814-191178864	LNCaP	prostate:	n/a
21	chr3:191178384-191178434	HCM	heart:	n/a
22	chr3:191178814-191178864	HNPCEpiC	eye:	n/a
23	chr3:191179074-191179124	SAEC	small airway:	n/a
24	chr3:191178384-191178434	Hepatocyte	liver:	n/a
25	chr3:191179074-191179124	HUVEC	blood vessel:	n/a
26	chr3:191178924-191178974	NHBE	bronchial:	n/a
27	chr3:191179074-191179124	K562	blood:	n/a
28	chr3:191179074-191179124	ProgFib	skin:	n/a
29	chr3:191178814-191178864	GM12878	blood:	n/a
30	chr3:191179074-191179124	HRCEpiC	kidney:	n/a
31	chr3:191178924-191178974	HRPEpiC	eye:	n/a
32	chr3:191179074-191179124	ovcar-3	ovarian:	n/a
33	chr3:191179074-191179124	AoSMC	blood vessel:	n/a
34	chr3:191178814-191178864	NHBE	bronchial:	n/a
35	chr3:191178814-191178864	HRPEpiC	eye:	n/a
36	chr3:191178924-191178974	GM12878	blood:	n/a
37	chr3:191178384-191178434	LNCaP	prostate:	n/a
38	chr3:191178924-191178974	AG10803	skin:	n/a
39	chr3:191178814-191178864	AG04450	lung:	fetal
40	chr3:191178924-191178974	HL-60	blood:	n/a
41	chr3:191178814-191178864	RPTEC	kidney:	n/a
42	chr3:191178814-191178864	HL-60	blood:	n/a
43	chr3:191179074-191179124	MCF-7	breast:	n/a
44	chr3:191179074-191179124	HL-60	blood:	n/a
45	chr3:191178924-191178974	SAEC	small airway:	n/a
46	chr3:191178384-191178434	NH-A	brain:	n/a
47	chr3:191178384-191178434	GM12891	blood:	n/a
48	chr3:191178814-191178864	SKMC	muscle:	n/a
49	chr3:191179074-191179124	NHBE	bronchial:	n/a
50	chr3:191179074-191179124	AG10803	skin:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:191154549..191157264-chr3:191174503..191176538,3	K562	blood:
2	chr3:191210173..191212267-chr3:191228106..191229922,2	K562	blood:
3	chr3:191194345..191196125-chr3:191201335..191204091,2	K562	blood:
4	chr3:191219513..191222335-chr3:191222361..191224281,2	MCF-7	breast:
5	chr3:191160341..191162761-chr3:191179942..191182380,2	K562	blood:
6	chr3:191186829..191191395-chr3:191192771..191196675,4	K562	blood:
7	chr3:191158609..191160577-chr3:191193167..191196023,2	K562	blood:
8	chr3:191202788..191205385-chr3:191217397..191220401,3	K562	blood:
9	chr3:191144312..191145933-chr3:191218364..191220735,2	K562	blood:
10	chr3:191187730..191193827-chr3:191193854..191197117,6	K562	blood:
11	chr3:191194345..191196125-chr3:191201335..191204091,2	K562	blood:
12	chr3:191220889..191222915-chr3:191232915..191235559,2	K562	blood:
13	chr3:191202788..191205385-chr3:191217397..191220401,3	K562	blood:
14	chr3:191161495..191163319-chr3:191214944..191216850,2	K562	blood:
15	chr3:191219513..191222335-chr3:191222361..191224281,2	MCF-7	breast:
16	chr3:191187730..191193827-chr3:191193854..191197117,6	K562	blood:
17	chr3:191220446..191222407-chr3:191229444..191232369,2	K562	blood:
18	chr3:191150064..191152045-chr3:191218500..191220211,2	K562	blood:
19	chr3:191144791..191146298-chr3:191179691..191181220,2	K562	blood:
20	chr3:191145766..191148014-chr3:191221969..191224844,2	K562	blood:
21	chr3:191142943..191145489-chr3:191191004..191192799,2	MCF-7	breast:
22	chr3:191223279..191226273-chr3:191227668..191229935,2	K562	blood:
23	chr3:191220103..191221050-chr3:191527147..191528017,3	MCF-7	breast:
24	chr3:191186829..191191395-chr3:191192771..191196675,4	K562	blood:

No data

Variant related genes	Relation type
PYDC2	TF binding region
PYDC2	CpG island

Extended variants
information (count: 1817 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1817 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs383815	chr3:191175215-191175216	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs408085	chr3:191175228-191175229	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs189364239	chr3:191175256-191175257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575183646	chr3:191175271-191175272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150425353	chr3:191175291-191175292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138166776	chr3:191175320-191175321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577199020	chr3:191175457-191175458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545865779	chr3:191175477-191175478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74684906	chr3:191175488-191175489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112887948	chr3:191175495-191175496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185129971	chr3:191175496-191175497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562226274	chr3:191175499-191175500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531129730	chr3:191175545-191175546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189770747	chr3:191175564-191175565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143858522	chr3:191175582-191175583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556739826	chr3:191175671-191175672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146306852	chr3:191175672-191175673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181193387	chr3:191175685-191175686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576584320	chr3:191175725-191175726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs9873118	chr3:191175726-191175727	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs186083659	chr3:191175735-191175736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188208944	chr3:191175736-191175737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568684063	chr3:191175781-191175782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143271523	chr3:191175798-191175799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558069734	chr3:191175809-191175810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571443948	chr3:191175868-191175869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs117788263	chr3:191175956-191175957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553360736	chr3:191176021-191176022	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs562055199	chr3:191176031-191176032	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs76817111	chr3:191176036-191176037	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs542311722	chr3:191176041-191176042	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs527636302	chr3:191176042-191176043	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs575828932	chr3:191176046-191176047	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs803045	chr3:191176092-191176093	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs709146	chr3:191176101-191176102	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs533411862	chr3:191176145-191176146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7633436	chr3:191176162-191176163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs386669607	chr3:191176167-191176168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs68072965	chr3:191176168-191176169	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs375325088	chr3:191176193-191176194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs782037	chr3:191176202-191176203	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs568847024	chr3:191176224-191176225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186262745	chr3:191176235-191176236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs386669608	chr3:191176248-191176249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs803046	chr3:191176249-191176250	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs534043844	chr3:191176263-191176264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553422131	chr3:191176274-191176275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs810634	chr3:191176284-191176285	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs201028820	chr3:191176310-191176311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs199644709	chr3:191176316-191176317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Lung cancer	19547694	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Optic atrophy	21457585	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-small cell lung cancer	21829676	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Recurrent pregnancy loss	19789632	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:191174000-191176400	Weak transcription	Stomach Mucosa	stomach
2	chr3:191174200-191175400	Strong transcription	K562	blood
3	chr3:191175400-191190200	Weak transcription	K562	blood
4	chr3:191176400-191177600	Enhancers	Stomach Mucosa	stomach
5	chr3:191179000-191179200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr3:191179200-191179600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:191181000-191181200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr3:191186400-191188800	Enhancers	Fetal Lung	lung
9	chr3:191187600-191188000	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr3:191187600-191188200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr3:191187600-191188200	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr3:191188000-191188800	Enhancers	Fetal Muscle Leg	muscle
13	chr3:191188000-191188800	Enhancers	Ovary	ovary
14	chr3:191188800-191193400	Weak transcription	Fetal Lung	lung
15	chr3:191190200-191191400	Enhancers	K562	blood
16	chr3:191191200-191192000	Enhancers	Hela-S3	cervix
17	chr3:191191400-191191600	Flanking Active TSS	K562	blood
18	chr3:191191600-191192000	Enhancers	K562	blood
19	chr3:191192000-191192400	Weak transcription	Hela-S3	cervix
20	chr3:191192000-191193400	Weak transcription	K562	blood
21	chr3:191192400-191194800	Enhancers	Hela-S3	cervix
22	chr3:191193400-191194000	Enhancers	Fetal Lung	lung
23	chr3:191193400-191194000	Enhancers	K562	blood
24	chr3:191194000-191194400	Weak transcription	Fetal Lung	lung
25	chr3:191194000-191195000	Genic enhancers	K562	blood
26	chr3:191194200-191194800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr3:191194200-191194800	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr3:191194200-191195000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr3:191194200-191195600	Enhancers	Stomach Mucosa	stomach
30	chr3:191194400-191195000	Enhancers	Fetal Lung	lung
31	chr3:191195000-191216600	Weak transcription	K562	blood
32	chr3:191195600-191201600	Weak transcription	Stomach Mucosa	stomach
33	chr3:191198000-191201800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr3:191201600-191202800	Enhancers	Stomach Mucosa	stomach
35	chr3:191201800-191203200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr3:191202000-191202800	Enhancers	NHEK	skin
37	chr3:191202000-191203400	Enhancers	HMEC	breast
38	chr3:191202200-191202600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr3:191202200-191202600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr3:191202200-191202600	Enhancers	Hela-S3	cervix
41	chr3:191202400-191202600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr3:191208400-191209600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr3:191209200-191210000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr3:191209600-191210000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr3:191209800-191211000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr3:191209800-191211000	Enhancers	HMEC	breast
47	chr3:191209800-191211800	Enhancers	Fetal Lung	lung
48	chr3:191210000-191211400	Enhancers	Fetal Heart	heart
49	chr3:191210200-191210800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr3:191210400-191210800	Enhancers	NHEK	skin

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