Variant report

Variant	nsv1002305
Chromosome Location	chr2:180568558-180812846
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1846)
CpG islands
(count:1593)
Chromatin interactive
region (count:94)
LncRNA
region (count:5)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1846 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:180702248-180702503	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:180812803-180813204	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:180801464-180801664	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:180664795-180664875	K562	blood:	n/a	n/a
5	ARID3A	chr2:180690273-180690547	K562	blood:	n/a	n/a
6	ARID3A	chr2:180661431-180661646	K562	blood:	n/a	n/a
7	ARID3A	chr2:180652341-180653120	K562	blood:	n/a	n/a
8	ARID3A	chr2:180615928-180616238	HepG2	liver:	n/a	n/a
9	ATF3	chr2:180690235-180690610	K562	blood:	n/a	n/a
10	BACH1	chr2:180664714-180664767	K562	blood:	n/a	n/a
11	BACH1	chr2:180782048-180782295	H1-hESC	embryonic stem cell:	n/a	chr2:180782187-180782201
12	BACH1	chr2:180578783-180578868	K562	blood:	n/a	n/a
13	BACH1	chr2:180725225-180725386	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr2:180725690-180725975	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr2:180682294-180682491	K562	blood:	n/a	n/a
16	BACH1	chr2:180809566-180809652	K562	blood:	n/a	n/a
17	BCL3	chr2:180682223-180682938	GM12878	blood:	n/a	n/a
18	BCL3	chr2:180682311-180682880	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:180763202-180763282	K562	blood:	n/a	n/a
20	BHLHE40	chr2:180804153-180804320	K562	blood:	n/a	n/a
21	BHLHE40	chr2:180707684-180707710	K562	blood:	n/a	n/a
22	BHLHE40	chr2:180807640-180807651	GM12878	blood:	n/a	n/a
23	BRCA1	chr2:180595028-180595071	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr2:180573906-180573981	GM12878	blood:	n/a	n/a
25	CBX3	chr2:180690188-180690672	K562	blood:	n/a	n/a
26	CBX3	chr2:180657906-180658660	K562	blood:	n/a	n/a
27	CBX3	chr2:180763589-180763971	HCT-116	colon:	n/a	n/a
28	CBX3	chr2:180652236-180652711	K562	blood:	n/a	n/a
29	CBX3	chr2:180790429-180790754	K562	blood:	n/a	n/a
30	CBX3	chr2:180790511-180790791	K562	blood:	n/a	n/a
31	CBX3	chr2:180790428-180790802	HCT-116	colon:	n/a	n/a
32	CBX3	chr2:180753446-180753754	K562	blood:	n/a	n/a
33	CBX3	chr2:180753394-180753724	K562	blood:	n/a	n/a
34	CBX3	chr2:180794756-180795038	K562	blood:	n/a	n/a
35	CCNT2	chr2:180652928-180653185	K562	blood:	n/a	chr2:180653037-180653057
36	CCNT2	chr2:180690193-180690574	K562	blood:	n/a	n/a
37	CCNT2	chr2:180808961-180809129	K562	blood:	n/a	n/a
38	CCNT2	chr2:180652281-180652662	K562	blood:	n/a	chr2:180652631-180652651
39	CCNT2	chr2:180728824-180729024	K562	blood:	n/a	n/a
40	CCNT2	chr2:180658016-180658238	K562	blood:	n/a	n/a
41	CCNT2	chr2:180723800-180723941	K562	blood:	n/a	n/a
42	CEBPB	chr2:180612811-180613062	K562	blood:	n/a	n/a
43	CEBPB	chr2:180612771-180612994	A549	lung:	n/a	chr2:180612792-180612805
44	CEBPB	chr2:180741550-180741789	IMR90	lung:	n/a	chr2:180741620-180741633 chr2:180741579-180741590
45	CEBPB	chr2:180615653-180616267	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr2:180741456-180741773	HepG2	liver:	n/a	chr2:180741620-180741633 chr2:180741579-180741590
47	CEBPB	chr2:180652843-180653209	K562	blood:	n/a	n/a
48	CEBPB	chr2:180615681-180616157	IMR90	lung:	n/a	n/a
49	CEBPB	chr2:180741506-180741771	A549	lung:	n/a	chr2:180741620-180741633 chr2:180741579-180741590
50	CEBPB	chr2:180690297-180690655	K562	blood:	n/a	n/a

(count:1593 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:180725645-180725695	ovcar-3	ovarian:	n/a
2	chr2:180726464-180726514	IMR90	lung:	fetal
3	chr2:180726252-180726302	BJ	skin:	n/a
4	chr2:180725637-180725687	HRE	kidney:	n/a
5	chr2:180678924-180678974	PANC-1	pancreas:	n/a
6	chr2:180726576-180726626	HCT-116	colon:	n/a
7	chr2:180726349-180726399	GM19239	blood:	n/a
8	chr2:180725645-180725695	ovcar-3	ovarian:	n/a
9	chr2:180726464-180726514	IMR90	lung:	fetal
10	chr2:180726252-180726302	BJ	skin:	n/a
11	chr2:180725637-180725687	HRE	kidney:	n/a
12	chr2:180678924-180678974	PANC-1	pancreas:	n/a
13	chr2:180726576-180726626	HCT-116	colon:	n/a
14	chr2:180726349-180726399	GM19239	blood:	n/a
15	chr2:180728398-180728448	HepG2	liver:	n/a
16	chr2:180728398-180728448	GM12891	blood:	n/a
17	chr2:180726464-180726514	PANC-1	pancreas:	n/a
18	chr2:180725718-180725768	ECC-1	luminal epithelium:	n/a
19	chr2:180730462-180730512	MCF-7	breast:	n/a
20	chr2:180725637-180725687	HEEpiC	esophagus:	n/a
21	chr2:180725691-180725741	GM12878	blood:	n/a
22	chr2:180613571-180613621	HRE	kidney:	n/a
23	chr2:180728398-180728448	AG09319	gingival:	n/a
24	chr2:180748603-180748653	ovcar-3	ovarian:	n/a
25	chr2:180613571-180613621	PFSK-1	brain:	n/a
26	chr2:180726697-180726747	PrEC	prostate:	n/a
27	chr2:180726328-180726378	AoSMC	blood vessel:	n/a
28	chr2:180725637-180725687	NB4	blood:	n/a
29	chr2:180726035-180726085	SK-N-MC	brain:	n/a
30	chr2:180725907-180725957	H1-hESC	embryonic stem cell:	embryo
31	chr2:180726464-180726514	HEEpiC	esophagus:	n/a
32	chr2:180725645-180725695	AoSMC	blood vessel:	n/a
33	chr2:180730462-180730512	RPTEC	kidney:	n/a
34	chr2:180727677-180727727	HL-60	blood:	n/a
35	chr2:180722610-180722660	HCM	heart:	n/a
36	chr2:180722610-180722660	BJ	skin:	n/a
37	chr2:180725637-180725687	GM06990	blood:	n/a
38	chr2:180725718-180725768	K562	blood:	n/a
39	chr2:180726252-180726302	H1-hESC	embryonic stem cell:	embryo
40	chr2:180726464-180726514	AG04450	lung:	fetal
41	chr2:180730462-180730512	Hepatocyte	liver:	n/a
42	chr2:180725691-180725741	MCF-7	breast:	n/a
43	chr2:180726035-180726085	CMK	blood:	n/a
44	chr2:180725691-180725741	AG04449	skin:	fetal
45	chr2:180727677-180727727	GM12891	blood:	n/a
46	chr2:180774797-180774847	BE2_C	brain:	n/a
47	chr2:180613571-180613621	CMK	blood:	n/a
48	chr2:180612012-180612062	AoSMC	blood vessel:	n/a
49	chr2:180726697-180726747	ECC-1	luminal epithelium:	n/a
50	chr2:180613571-180613621	HIPEpiC	eye:	n/a

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:180707295..180707909-chr2:180763473..180764251,2	MCF-7	breast:
2	chr2:180645503..180649347-chr2:180649470..180653497,3	K562	blood:
3	chr2:180083839..180084369-chr2:180763413..180764243,2	K562	blood:
4	chr2:180743150..180746024-chr2:180754636..180757540,3	K562	blood:
5	chr2:180664595..180667266-chr2:180669827..180672570,2	K562	blood:
6	chr2:180704558..180706677-chr2:180713016..180714537,2	MCF-7	breast:
7	chr2:180658967..180660810-chr2:180663202..180665986,2	MCF-7	breast:
8	chr2:180738640..180741143-chr2:180742464..180744446,2	K562	blood:
9	chr2:180635759..180637843-chr2:180643874..180645824,2	MCF-7	breast:
10	chr2:180628206..180630948-chr2:180635078..180637285,2	K562	blood:
11	chr2:180706972..180707878-chr2:180763320..180764150,2	MCF-7	breast:
12	chr2:180645503..180649347-chr2:180649470..180653497,3	K562	blood:
13	chr2:180808241..180810462-chr2:180810582..180812457,2	MCF-7	breast:
14	chr2:180664595..180667266-chr2:180669827..180672570,2	K562	blood:
15	chr2:180800902..180803071-chr2:180803313..180806078,2	K562	blood:
16	chr2:180710308..180712381-chr2:180720842..180723384,2	K562	blood:
17	chr2:180709707..180712515-chr2:180716241..180718781,2	K562	blood:
18	chr2:180656227..180658601-chr2:180661307..180663492,2	K562	blood:
19	chr2:180707129..180707861-chr2:180763387..180764295,2	K562	blood:
20	chr2:180812825..180815255-chr2:180816104..180818371,2	K562	blood:
21	chr2:180286529..180287408-chr2:180615709..180616559,2	K562	blood:
22	chr2:180706968..180707872-chr2:180831565..180832499,2	MCF-7	breast:
23	chr2:180706168..180708341-chr2:180711093..180713264,3	K562	blood:
24	chr2:180800902..180803071-chr2:180803313..180806078,2	K562	blood:
25	chr2:180707163..180707821-chr2:180941894..180942731,3	MCF-7	breast:
26	chr2:180602698..180605470-chr2:180624770..180626528,2	K562	blood:
27	chr2:179278797..179281186-chr2:180773348..180774954,2	K562	blood:
28	chr2:180707046..180707794-chr2:180801109..180802085,4	MCF-7	breast:
29	chr2:180709707..180712515-chr2:180716241..180718781,2	K562	blood:
30	chr2:180707129..180707861-chr2:180763387..180764295,2	K562	blood:
31	chr2:180804951..180807735-chr2:180812353..180814788,2	K562	blood:
32	chr16:24144309..24145158-chr2:180665114..180665649,2	MCF-7	breast:
33	chr2:180584134..180586759-chr2:180588333..180591322,3	K562	blood:
34	chr2:179660477..179661475-chr2:180615670..180616601,3	K562	blood:
35	chr2:180707046..180707794-chr2:180801109..180802085,4	MCF-7	breast:
36	chr2:180683248..180686048-chr2:180688712..180690525,2	K562	blood:
37	chr2:180286493..180287715-chr2:180615528..180616540,6	MCF-7	breast:
38	chr2:180710308..180712381-chr2:180720842..180723384,2	K562	blood:
39	chr2:180652099..180653752-chr2:180660144..180662065,2	K562	blood:
40	chr2:179660873..179661497-chr2:180616030..180616590,2	MCF-7	breast:
41	chr2:180658967..180660810-chr2:180663202..180665986,2	MCF-7	breast:
42	chr2:180584134..180586759-chr2:180588333..180591322,3	K562	blood:
43	chr2:180744922..180746491-chr2:180749766..180752592,2	MCF-7	breast:
44	chr2:180810446..180815338-chr2:180815849..180820323,6	K562	blood:
45	chr2:180697026..180699896-chr2:180705650..180708149,2	MCF-7	breast:
46	chr2:180663219..180666170-chr2:180666828..180669197,2	K562	blood:
47	chr2:180630128..180633028-chr2:180639169..180641333,2	K562	blood:
48	chr2:180796072..180797988-chr2:180799207..180801113,2	K562	blood:
49	chr2:180711911..180714659-chr2:180717451..180719062,2	MCF-7	breast:
50	chr2:180721435..180722983-chr2:180725390..180727274,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UBE2E3-9	chr2:180808757-180808919	NONHSAT075835
2	lnc-UBE2E3-9	chr2:180729067-180729484	NONHSAT075835
3	lnc-UBE2E3-3	chr2:180782080-180782371	XLOC_001772
4	lnc-UBE2E3-3	chr2:180764787-180764889	XLOC_001772
5	lnc-UBE2E3-8	chr2:180800420-180800998	NONHSAT075838

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1258	chr2:180725572-180725592	MIMAT0005909

No data

Variant related genes	Relation type
MIR1258	TF binding region
ENSG00000202216	TF binding region
ZNF385B	TF binding region
ENSG00000213126	TF binding region
MIR1258	CpG island
ENSG00000202216	CpG island
ZNF385B	CpG island
ENSG00000213126	CpG island
ENSG00000144331	chromatin interactions
ENSG00000221240	chromatin interactions
ENSG00000202216	chromatin interactions
ENSG00000163510	chromatin interactions
HPSE	Mature miRNA region

Extended variants
information (count: 6864 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:6864 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184132203	chr2:180568581-180568582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs577637643	chr2:180568595-180568596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543127747	chr2:180568614-180568615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563949302	chr2:180568635-180568636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144612789	chr2:180568643-180568644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148498151	chr2:180568683-180568684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560046952	chr2:180568711-180568712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528514834	chr2:180568731-180568732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs551773893	chr2:180568743-180568744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs75568311	chr2:180568760-180568761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546091373	chr2:180568799-180568800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73973682	chr2:180568850-180568851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186538898	chr2:180568872-180568873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569877710	chr2:180568927-180568928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs367996910	chr2:180568954-180568955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144199266	chr2:180568969-180568970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs13415480	chr2:180568975-180568976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2008230	chr2:180568986-180568987	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs558176190	chr2:180569013-180569014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74555840	chr2:180569082-180569083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537197426	chr2:180569094-180569095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12470217	chr2:180569100-180569101	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs574294737	chr2:180569154-180569155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs746701	chr2:180569195-180569196	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs549103082	chr2:180569196-180569197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573609343	chr2:180569205-180569206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545364494	chr2:180569209-180569210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190947289	chr2:180569222-180569223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530806385	chr2:180569238-180569239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551054473	chr2:180569241-180569242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs114803602	chr2:180569277-180569278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369749005	chr2:180569398-180569399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529069026	chr2:180569412-180569413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548738572	chr2:180569423-180569424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116730995	chr2:180569438-180569439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375518289	chr2:180569443-180569444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183192773	chr2:180569459-180569460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551384285	chr2:180569463-180569464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75084254	chr2:180569464-180569465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs79028995	chr2:180569538-180569539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563595320	chr2:180569560-180569561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187486641	chr2:180569605-180569606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146561920	chr2:180569709-180569710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114585716	chr2:180569725-180569726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553639663	chr2:180569748-180569749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563928378	chr2:180569793-180569794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374789736	chr2:180569801-180569802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553215048	chr2:180569834-180569835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573468481	chr2:180569841-180569842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192927427	chr2:180569850-180569851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Schizophrenia	19348701	CNVD
Muscular dystrophy	17160897	CNVD
Cardiomyopathy	17576883	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1127 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180540400-180571200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:180568000-180568600	Weak transcription	HSMMtube	muscle
3	chr2:180568000-180572200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:180568200-180569200	Weak transcription	Liver	Liver
5	chr2:180568600-180568800	Enhancers	HSMMtube	muscle
6	chr2:180569400-180569600	Enhancers	Liver	Liver
7	chr2:180571200-180571600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:180571600-180577600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:180572200-180574400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:180572400-180572600	Enhancers	Lung	lung
11	chr2:180572400-180572600	Enhancers	Right Atrium	heart
12	chr2:180572600-180574600	Weak transcription	Lung	lung
13	chr2:180572600-180582200	Weak transcription	Right Atrium	heart
14	chr2:180572800-180573000	Enhancers	Gastric	stomach
15	chr2:180573000-180576000	Weak transcription	Gastric	stomach
16	chr2:180573200-180576800	Enhancers	Placenta Amnion	Placenta Amnion
17	chr2:180573600-180574000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr2:180573800-180574200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:180574000-180576400	Weak transcription	Stomach Smooth Muscle	stomach
20	chr2:180574600-180575200	ZNF genes & repeats	Lung	lung
21	chr2:180575200-180576000	Enhancers	Placenta	Placenta
22	chr2:180575400-180576400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr2:180575600-180576000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr2:180575600-180576000	Enhancers	NHEK	skin
25	chr2:180575800-180576200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:180576000-180576800	Enhancers	HSMMtube	muscle
27	chr2:180580600-180581600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr2:180581400-180582200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr2:180582200-180582400	Enhancers	Right Atrium	heart
30	chr2:180582400-180585600	Weak transcription	Right Atrium	heart
31	chr2:180583800-180584400	Enhancers	H9 Cell Line	embryonic stem cell
32	chr2:180584000-180584200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr2:180584000-180584200	Enhancers	HepG2	liver
34	chr2:180585600-180585800	Enhancers	Right Atrium	heart
35	chr2:180591000-180591800	Enhancers	Placenta Amnion	Placenta Amnion
36	chr2:180594800-180595400	Enhancers	Liver	Liver
37	chr2:180604200-180608600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr2:180604800-180607000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr2:180607000-180607400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr2:180607400-180607600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr2:180607600-180610000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr2:180608600-180608800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr2:180608600-180611200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr2:180608800-180610800	Active TSS	Right Atrium	heart
45	chr2:180608800-180613000	Enhancers	Fetal Lung	lung
46	chr2:180609600-180611000	Active TSS	Brain Inferior Temporal Lobe	brain
47	chr2:180610000-180610200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr2:180610000-180610200	Enhancers	Brain Angular Gyrus	brain
49	chr2:180610000-180610400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
50	chr2:180610200-180610800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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