Variant report

Variant	nsv877781
Chromosome Location	chr3:162664345-162754958
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	BRCA1	chr3:162717002-162717061	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr3:162695964-162696261	HepG2	liver:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
3	CEBPB	chr3:162695952-162696294	A549	lung:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
4	CEBPB	chr3:162695982-162696258	H1-hESC	embryonic stem cell:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
5	CEBPB	chr3:162729220-162729874	MCF-7	breast:	n/a	n/a
6	CEBPB	chr3:162711790-162712125	HepG2	liver:	n/a	chr3:162711927-162711938
7	CEBPB	chr3:162682141-162682443	A549	lung:	n/a	chr3:162682288-162682299
8	CEBPB	chr3:162729522-162729600	A549	lung:	n/a	n/a
9	CEBPB	chr3:162682143-162682476	HepG2	liver:	n/a	chr3:162682288-162682299
10	CEBPB	chr3:162695972-162696288	IMR90	lung:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
11	CEBPB	chr3:162729383-162729666	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr3:162695893-162696380	MCF-7	breast:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
13	CEBPB	chr3:162729092-162729733	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr3:162711839-162712097	IMR90	lung:	n/a	chr3:162711927-162711938
15	CEBPB	chr3:162696009-162696307	A549	lung:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
16	CEBPB	chr3:162682128-162682457	IMR90	lung:	n/a	chr3:162682288-162682299
17	CEBPB	chr3:162682187-162682344	K562	blood:	n/a	chr3:162682288-162682299
18	CEBPB	chr3:162729049-162729851	MCF-7	breast:	n/a	n/a
19	CEBPB	chr3:162695846-162696372	A549	lung:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
20	CEBPB	chr3:162696021-162696193	K562	blood:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
21	CEBPB	chr3:162695938-162696308	MCF-7	breast:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
22	CTCF	chr3:162697458-162697485	GM20000	blood:	n/a	n/a
23	CTCF	chr3:162666278-162666325	GM20000	blood:	n/a	n/a
24	CTCF	chr3:162742000-162742150	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr3:162707965-162708006	MCF-7	breast:	n/a	n/a
26	CTCF	chr3:162715960-162716110	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr3:162670719-162670752	LNCaP	prostate:	n/a	n/a
28	CTCF	chr3:162753290-162753354	GM13976	blood:	n/a	n/a
29	CUX1	chr3:162730188-162730192	K562	blood:	n/a	n/a
30	E2F4	chr3:162753864-162753982	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr3:162671159-162671351	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr3:162739552-162739907	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr3:162742908-162743235	MCF10A-Er-Src	breast:	n/a	n/a
34	EGR1	chr3:162729339-162729821	MCF-7	breast:	n/a	n/a
35	EP300	chr3:162729337-162729872	MCF-7	breast:	n/a	chr3:162729395-162729409 chr3:162729394-162729408
36	EP300	chr3:162729442-162729816	MCF-7	breast:	n/a	n/a
37	EP300	chr3:162664578-162665055	MCF-7	breast:	n/a	n/a
38	EP300	chr3:162729436-162729796	T-47D	breast:	n/a	n/a
39	EP300	chr3:162710695-162710812	GM12878	blood:	n/a	n/a
40	EP300	chr3:162687939-162688274	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr3:162729410-162729811	T-47D	breast:	n/a	n/a
42	EP300	chr3:162710706-162710794	GM12878	blood:	n/a	n/a
43	ESR1	chr3:162729405-162729760	T-47D	breast:	n/a	n/a
44	FOS	chr3:162695961-162696319	MCF10A-Er-Src	breast:	n/a	chr3:162696150-162696160
45	FOS	chr3:162667421-162667621	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr3:162733027-162733171	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr3:162695962-162696314	MCF10A-Er-Src	breast:	n/a	chr3:162696150-162696160
48	FOS	chr3:162667459-162667659	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr3:162695909-162696357	MCF10A-Er-Src	breast:	n/a	chr3:162696150-162696160
50	FOS	chr3:162667459-162667645	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:162705337-162705387	AG09309	skin:	n/a
2	chr3:162705337-162705387	IMR90	lung:	fetal
3	chr3:162705203-162705253	HCT-116	colon:	n/a
4	chr3:162705337-162705387	HRE	kidney:	n/a
5	chr3:162705427-162705477	AG04449	skin:	fetal
6	chr3:162705337-162705387	MCF-7	breast:	n/a
7	chr3:162705337-162705387	SAEC	small airway:	n/a
8	chr3:162705203-162705253	A549	lung:	n/a
9	chr3:162705427-162705477	AoSMC	blood vessel:	n/a
10	chr3:162705203-162705253	HRE	kidney:	n/a
11	chr3:162705203-162705253	HUVEC	blood vessel:	n/a
12	chr3:162705203-162705253	SKMC	muscle:	n/a
13	chr3:162705427-162705477	Hepatocyte	liver:	n/a
14	chr3:162705427-162705477	NB4	blood:	n/a
15	chr3:162705427-162705477	BE2_C	brain:	n/a
16	chr3:162705427-162705477	PANC-1	pancreas:	n/a
17	chr3:162705427-162705477	MCF-7	breast:	n/a
18	chr3:162705203-162705253	AG09319	gingival:	n/a
19	chr3:162705427-162705477	SK-N-MC	brain:	n/a
20	chr3:162705337-162705387	PFSK-1	brain:	n/a
21	chr3:162705337-162705387	GM19239	blood:	n/a
22	chr3:162705427-162705477	HCF	heart:	n/a
23	chr3:162705337-162705387	GM12878	blood:	n/a
24	chr3:162705427-162705477	U87	brain:	n/a
25	chr3:162705427-162705477	SK-N-SH	brain:	n/a
26	chr3:162705203-162705253	HNPCEpiC	eye:	n/a
27	chr3:162705337-162705387	HIPEpiC	eye:	n/a
28	chr3:162705203-162705253	BJ	skin:	n/a
29	chr3:162705337-162705387	GM12892	blood:	n/a
30	chr3:162705203-162705253	PFSK-1	brain:	n/a
31	chr3:162705203-162705253	BE2_C	brain:	n/a
32	chr3:162705203-162705253	AG09309	skin:	n/a
33	chr3:162705337-162705387	MCF10A-Er-Src	breast:	n/a
34	chr3:162705427-162705477	AG09309	skin:	n/a
35	chr3:162705337-162705387	Hela-S3	cervix:	n/a
36	chr3:162705337-162705387	PrEC	prostate:	n/a
37	chr3:162705203-162705253	GM12891	blood:	n/a
38	chr3:162705337-162705387	SK-N-MC	brain:	n/a
39	chr3:162705337-162705387	ProgFib	skin:	n/a
40	chr3:162705427-162705477	HNPCEpiC	eye:	n/a
41	chr3:162705427-162705477	GM06990	blood:	n/a
42	chr3:162705427-162705477	Hela-S3	cervix:	n/a
43	chr3:162705427-162705477	H1-hESC	embryonic stem cell:	embryo
44	chr3:162705203-162705253	ovcar-3	ovarian:	n/a
45	chr3:162705427-162705477	SK-N-SH_RA	brain:	n/a
46	chr3:162705427-162705477	GM19239	blood:	n/a
47	chr3:162705337-162705387	AG04450	lung:	fetal
48	chr3:162705203-162705253	Jurkat	blood:	n/a
49	chr3:162705337-162705387	HEK293	kidney:	embryo
50	chr3:162705337-162705387	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:162730866..162732605-chr3:162732763..162734314,2	MCF-7	breast:
2	chr3:162730866..162732605-chr3:162732763..162734314,2	MCF-7	breast:
3	chr3:162695238..162696118-chr5:168564460..168564967,2	MCF-7	breast:
4	chr3:162692633..162695202-chr3:162700914..162703834,2	MCF-7	breast:
5	chr14:60627662..60628534-chr3:162740219..162740719,2	MCF-7	breast:
6	chr3:162692633..162695202-chr3:162700914..162703834,2	MCF-7	breast:
7	chr20:11421691..11422663-chr3:162694553..162695419,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OTOL1-2	chr3:162744184-162744286	ENSG00000241168.1
2	lnc-OTOL1-2	chr3:162744184-162744286	NONHSAT093026

Variant related genes	Relation type
ENSG00000241168	TF binding region
ENSG00000241168	CpG island

Extended variants
information (count: 2087 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2087 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9845104	chr3:162664345-162664346	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563867804	chr3:162664376-162664377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529452185	chr3:162664414-162664415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140220974	chr3:162664475-162664476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547735391	chr3:162664496-162664497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs552887130	chr3:162664515-162664516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143435819	chr3:162664535-162664536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150941048	chr3:162664540-162664541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548242106	chr3:162664575-162664576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183266187	chr3:162664581-162664582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs68161621	chr3:162664602-162664603	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs140772612	chr3:162664607-162664608	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs569500383	chr3:162664631-162664632	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs73023181	chr3:162664636-162664637	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs150126619	chr3:162664655-162664656	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs572203301	chr3:162664696-162664697	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs541033515	chr3:162664703-162664704	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs186841459	chr3:162664737-162664738	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs73023183	chr3:162664740-162664741	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs543519919	chr3:162664794-162664795	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs142812965	chr3:162664802-162664803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147002309	chr3:162664806-162664807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546390732	chr3:162664813-162664814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559997352	chr3:162664851-162664852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528739383	chr3:162664875-162664876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563538069	chr3:162664950-162664951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138184298	chr3:162664975-162664976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561913201	chr3:162664979-162664980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs67895998	chr3:162665042-162665043	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs199532262	chr3:162665049-162665050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs73023185	chr3:162665066-162665067	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs532212904	chr3:162665115-162665116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538447335	chr3:162665142-162665143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552042602	chr3:162665192-162665193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377367821	chr3:162665230-162665231	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73023187	chr3:162665258-162665259	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs534613529	chr3:162665313-162665314	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191723972	chr3:162665332-162665333	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567786822	chr3:162665403-162665404	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs12636307	chr3:162665409-162665410	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs537010565	chr3:162665414-162665415	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs370395326	chr3:162665430-162665431	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs555900187	chr3:162665441-162665442	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs144671651	chr3:162665471-162665472	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs184234452	chr3:162665489-162665490	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs148519463	chr3:162665517-162665518	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs559689851	chr3:162665559-162665560	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs377274305	chr3:162665609-162665610	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs573507715	chr3:162665641-162665642	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs67960907	chr3:162665643-162665644	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:63)

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	22032731	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
head and neck squamous cell carcinoma	17671120	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Sudden cardiac death	19188705	CNVD
Mantle cell lymphoma	19029149	CNVD
Malformation	19546859	CNVD
Schizophrenia	19546859	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:162654400-162665200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr3:162662800-162664600	Weak transcription	Aorta	Aorta
3	chr3:162663600-162665400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr3:162664600-162664800	ZNF genes & repeats	Aorta	Aorta
5	chr3:162665200-162665800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
6	chr3:162665400-162666000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
7	chr3:162665600-162665800	ZNF genes & repeats	Aorta	Aorta
8	chr3:162666000-162666800	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr3:162674800-162675200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr3:162676400-162681800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr3:162681800-162682400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
12	chr3:162683800-162684200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
13	chr3:162683800-162684400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
14	chr3:162690200-162692200	Enhancers	Dnd41	blood
15	chr3:162691200-162691800	Enhancers	A549	lung
16	chr3:162691800-162695400	Weak transcription	A549	lung
17	chr3:162695400-162696200	Enhancers	A549	lung
18	chr3:162702200-162702600	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr3:162702400-162702600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr3:162702400-162702800	Enhancers	Aorta	Aorta
21	chr3:162702400-162702800	Active TSS	Hela-S3	cervix
22	chr3:162702400-162703000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr3:162702600-162702800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
24	chr3:162702600-162703200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr3:162703200-162704800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
26	chr3:162704800-162707800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr3:162710600-162710800	Enhancers	Dnd41	blood
28	chr3:162710800-162711000	Weak transcription	Dnd41	blood
29	chr3:162711000-162713600	ZNF genes & repeats	Dnd41	blood
30	chr3:162713600-162714400	Weak transcription	Dnd41	blood
31	chr3:162714400-162714800	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr3:162714400-162715200	Enhancers	Dnd41	blood
33	chr3:162715200-162716400	Flanking Active TSS	Dnd41	blood
34	chr3:162715400-162716000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr3:162715400-162716200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr3:162715400-162716200	Enhancers	Colon Smooth Muscle	Colon
37	chr3:162715400-162716200	Active TSS	Duodenum Smooth Muscle	Duodenum
38	chr3:162715600-162715800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr3:162715600-162716000	Active TSS	Adipose Nuclei	Adipose
40	chr3:162715600-162716000	Active TSS	Aorta	Aorta
41	chr3:162715600-162716000	Active TSS	Rectal Mucosa Donor 29	rectum
42	chr3:162715600-162716000	Active TSS	Stomach Smooth Muscle	stomach
43	chr3:162715600-162716200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr3:162715600-162716200	Active TSS	Brain Inferior Temporal Lobe	brain
45	chr3:162715600-162716800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr3:162715800-162716000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr3:162715800-162716600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr3:162715800-162716600	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr3:162716000-162716200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr3:162716000-162716200	Weak transcription	Rectal Mucosa Donor 29	rectum

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