Variant report

Variant	nsv428731
Chromosome Location	chr2:180629389-180805171
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1477)
CpG islands
(count:1467)
Chromatin interactive
region (count:69)
LncRNA
region (count:4)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1477 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:180801464-180801664	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:180661431-180661646	K562	blood:	n/a	n/a
3	ARID3A	chr2:180664795-180664875	K562	blood:	n/a	n/a
4	ARID3A	chr2:180690273-180690547	K562	blood:	n/a	n/a
5	ARID3A	chr2:180702248-180702503	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:180652341-180653120	K562	blood:	n/a	n/a
7	ATF3	chr2:180690235-180690610	K562	blood:	n/a	n/a
8	BACH1	chr2:180725225-180725386	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:180664714-180664767	K562	blood:	n/a	n/a
10	BACH1	chr2:180725690-180725975	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:180782048-180782295	H1-hESC	embryonic stem cell:	n/a	chr2:180782187-180782201
12	BACH1	chr2:180682294-180682491	K562	blood:	n/a	n/a
13	BCL3	chr2:180682223-180682938	GM12878	blood:	n/a	n/a
14	BCL3	chr2:180682311-180682880	GM12878	blood:	n/a	n/a
15	BHLHE40	chr2:180804153-180804320	K562	blood:	n/a	n/a
16	BHLHE40	chr2:180763202-180763282	K562	blood:	n/a	n/a
17	BHLHE40	chr2:180707684-180707710	K562	blood:	n/a	n/a
18	CBX3	chr2:180753446-180753754	K562	blood:	n/a	n/a
19	CBX3	chr2:180690188-180690672	K562	blood:	n/a	n/a
20	CBX3	chr2:180753394-180753724	K562	blood:	n/a	n/a
21	CBX3	chr2:180790428-180790802	HCT-116	colon:	n/a	n/a
22	CBX3	chr2:180652236-180652711	K562	blood:	n/a	n/a
23	CBX3	chr2:180790429-180790754	K562	blood:	n/a	n/a
24	CBX3	chr2:180794756-180795038	K562	blood:	n/a	n/a
25	CBX3	chr2:180657906-180658660	K562	blood:	n/a	n/a
26	CBX3	chr2:180790511-180790791	K562	blood:	n/a	n/a
27	CBX3	chr2:180763589-180763971	HCT-116	colon:	n/a	n/a
28	CCNT2	chr2:180723800-180723941	K562	blood:	n/a	n/a
29	CCNT2	chr2:180728824-180729024	K562	blood:	n/a	n/a
30	CCNT2	chr2:180652928-180653185	K562	blood:	n/a	chr2:180653037-180653057
31	CCNT2	chr2:180652281-180652662	K562	blood:	n/a	chr2:180652631-180652651
32	CCNT2	chr2:180690193-180690574	K562	blood:	n/a	n/a
33	CCNT2	chr2:180658016-180658238	K562	blood:	n/a	n/a
34	CEBPB	chr2:180639769-180640055	K562	blood:	n/a	n/a
35	CEBPB	chr2:180801479-180801728	MCF-7	breast:	n/a	n/a
36	CEBPB	chr2:180801410-180801715	HepG2	liver:	n/a	n/a
37	CEBPB	chr2:180665571-180665834	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr2:180699882-180700144	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:180634844-180635094	Hela-S3	cervix:	n/a	chr2:180634952-180634963
40	CEBPB	chr2:180774510-180774878	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:180765724-180765949	A549	lung:	n/a	chr2:180765848-180765859
42	CEBPB	chr2:180690297-180690655	K562	blood:	n/a	n/a
43	CEBPB	chr2:180652420-180653163	K562	blood:	n/a	n/a
44	CEBPB	chr2:180679613-180679664	HepG2	liver:	n/a	chr2:180679625-180679636
45	CEBPB	chr2:180782089-180782308	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr2:180775099-180775446	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:180741456-180741773	HepG2	liver:	n/a	chr2:180741620-180741633 chr2:180741579-180741590
48	CEBPB	chr2:180641162-180641459	K562	blood:	n/a	chr2:180641328-180641341 chr2:180641329-180641340 chr2:180641328-180641341 chr2:180641328-180641339
49	CEBPB	chr2:180690202-180690659	K562	blood:	n/a	n/a
50	CEBPB	chr2:180725925-180725955	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:180726328-180726378	SK-N-SH_RA	brain:	n/a
2	chr2:180726328-180726378	SK-N-MC	brain:	n/a
3	chr2:180725718-180725768	LNCaP	prostate:	n/a
4	chr2:180726328-180726378	SK-N-SH_RA	brain:	n/a
5	chr2:180726328-180726378	SK-N-MC	brain:	n/a
6	chr2:180725718-180725768	LNCaP	prostate:	n/a
7	chr2:180748603-180748653	Hela-S3	cervix:	n/a
8	chr2:180748603-180748653	NH-A	brain:	n/a
9	chr2:180726247-180726297	NH-A	brain:	n/a
10	chr2:180725907-180725957	HIPEpiC	eye:	n/a
11	chr2:180712208-180712258	AoSMC	blood vessel:	n/a
12	chr2:180678924-180678974	HMEC	breast:	n/a
13	chr2:180726249-180726299	HRPEpiC	eye:	n/a
14	chr2:180726464-180726514	ProgFib	skin:	n/a
15	chr2:180726464-180726514	GM12891	blood:	n/a
16	chr2:180726035-180726085	HPAEpiC	pulmonary alveolar:	n/a
17	chr2:180722610-180722660	GM19239	blood:	n/a
18	chr2:180725622-180725672	HAEpiC	amniotic membrane:	n/a
19	chr2:180726328-180726378	SKMC	muscle:	n/a
20	chr2:180725718-180725768	AG04449	skin:	fetal
21	chr2:180726464-180726514	H1-hESC	embryonic stem cell:	embryo
22	chr2:180678924-180678974	Hela-S3	cervix:	n/a
23	chr2:180712208-180712258	MCF-7	breast:	n/a
24	chr2:180725622-180725672	SK-N-MC	brain:	n/a
25	chr2:180712208-180712258	Hepatocyte	liver:	n/a
26	chr2:180725907-180725957	NB4	blood:	n/a
27	chr2:180726252-180726302	SK-N-SH	brain:	n/a
28	chr2:180726249-180726299	AG09319	gingival:	n/a
29	chr2:180726697-180726747	NH-A	brain:	n/a
30	chr2:180726035-180726085	T-47D	breast:	n/a
31	chr2:180726697-180726747	HPAEpiC	pulmonary alveolar:	n/a
32	chr2:180722610-180722660	AG04449	skin:	fetal
33	chr2:180725645-180725695	SK-N-SH	brain:	n/a
34	chr2:180726464-180726514	HMEC	breast:	n/a
35	chr2:180712208-180712258	RPTEC	kidney:	n/a
36	chr2:180726247-180726297	GM12892	blood:	n/a
37	chr2:180726328-180726378	HEK293	kidney:	embryo
38	chr2:180722610-180722660	HMEC	breast:	n/a
39	chr2:180725718-180725768	HIPEpiC	eye:	n/a
40	chr2:180726252-180726302	NHBE	bronchial:	n/a
41	chr2:180711137-180711187	NT2-D1	testis:	n/a
42	chr2:180726247-180726297	ECC-1	luminal epithelium:	n/a
43	chr2:180726576-180726626	U87	brain:	n/a
44	chr2:180726249-180726299	Caco-2	colon:	n/a
45	chr2:180678924-180678974	T-47D	breast:	n/a
46	chr2:180726349-180726399	MCF-7	breast:	n/a
47	chr2:180725637-180725687	IMR90	lung:	fetal
48	chr2:180726247-180726297	U87	brain:	n/a
49	chr2:180726249-180726299	SKMC	muscle:	n/a
50	chr2:180725691-180725741	HepG2	liver:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:180628206..180630948-chr2:180635078..180637285,2	K562	blood:
2	chr2:180706972..180707878-chr2:180763320..180764150,2	MCF-7	breast:
3	chr2:180711911..180714659-chr2:180717451..180719062,2	MCF-7	breast:
4	chr2:180709707..180712515-chr2:180716241..180718781,2	K562	blood:
5	chr2:180707046..180707794-chr2:180801109..180802085,4	MCF-7	breast:
6	chr2:180707046..180707794-chr2:180801109..180802085,4	MCF-7	breast:
7	chr2:180804951..180807735-chr2:180812353..180814788,2	K562	blood:
8	chr2:180635759..180637843-chr2:180643874..180645824,2	MCF-7	breast:
9	chr2:179626506..179627084-chr2:180801448..180802026,2	MCF-7	breast:
10	chr2:180707163..180707821-chr2:180941894..180942731,3	MCF-7	breast:
11	chr2:180738640..180741143-chr2:180742464..180744446,2	K562	blood:
12	chr2:180706168..180708341-chr2:180711093..180713264,3	K562	blood:
13	chr2:180744922..180746491-chr2:180749766..180752592,2	MCF-7	breast:
14	chr2:180687765..180690198-chr2:180866903..180869093,2	K562	blood:
15	chr2:180800902..180803071-chr2:180803313..180806078,2	K562	blood:
16	chr2:180710308..180712381-chr2:180720842..180723384,2	K562	blood:
17	chr2:180630128..180633028-chr2:180639169..180641333,2	K562	blood:
18	chr2:180697026..180699896-chr2:180705650..180708149,2	MCF-7	breast:
19	chr2:180627157..180629783-chr2:180633092..180634769,2	K562	blood:
20	chr2:180704558..180706677-chr2:180713016..180714537,2	MCF-7	breast:
21	chr2:180743150..180746024-chr2:180754636..180757540,3	K562	blood:
22	chr2:180656227..180658601-chr2:180661307..180663492,2	K562	blood:
23	chr2:180628587..180630294-chr2:180645560..180647157,2	K562	blood:
24	chr2:180707129..180707861-chr2:180763387..180764295,2	K562	blood:
25	chr2:180796072..180797988-chr2:180799207..180801113,2	K562	blood:
26	chr2:180771436..180773113-chr2:180774837..180777642,2	K562	blood:
27	chr2:180709707..180712515-chr2:180716241..180718781,2	K562	blood:
28	chr2:180724511..180728493-chr2:180729164..180732918,3	MCF-7	breast:
29	chr2:180706168..180708341-chr2:180711093..180713264,3	K562	blood:
30	chr2:180706968..180707872-chr2:180831565..180832499,2	MCF-7	breast:
31	chr2:180636066..180638013-chr2:180660041..180662260,2	K562	blood:
32	chr2:180676125..180678431-chr2:180681304..180683534,2	K562	blood:
33	chr2:180652099..180653752-chr2:180660144..180662065,2	K562	blood:
34	chr2:180707295..180707909-chr2:180763473..180764251,2	MCF-7	breast:
35	chr2:180707295..180707909-chr2:180763473..180764251,2	MCF-7	breast:
36	chr2:180706972..180707878-chr2:180763320..180764150,2	MCF-7	breast:
37	chr2:180721435..180722983-chr2:180725390..180727274,2	K562	blood:
38	chr2:180628587..180630294-chr2:180645560..180647157,2	K562	blood:
39	chr2:180656227..180658601-chr2:180661307..180663492,2	K562	blood:
40	chr2:180738640..180741143-chr2:180742464..180744446,2	K562	blood:
41	chr2:180683248..180686048-chr2:180688712..180690525,2	K562	blood:
42	chr2:180676125..180678431-chr2:180681304..180683534,2	K562	blood:
43	chr2:180663219..180666170-chr2:180666828..180669197,2	K562	blood:
44	chr2:179278797..179281186-chr2:180773348..180774954,2	K562	blood:
45	chr2:179623890..179625824-chr2:180736631..180738464,2	K562	blood:
46	chr2:180635759..180637843-chr2:180643874..180645824,2	MCF-7	breast:
47	chr2:180664595..180667266-chr2:180669827..180672570,2	K562	blood:
48	chr2:180658967..180660810-chr2:180663202..180665986,2	MCF-7	breast:
49	chr2:180800902..180803071-chr2:180803313..180806078,2	K562	blood:
50	chr2:180083839..180084369-chr2:180763413..180764243,2	K562	blood:

(count:4 , 50 per page) page: 1

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

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
ENSG00000221240	chromatin interactions
ENSG00000202216	chromatin interactions
ENSG00000144331	chromatin interactions
HPSE	Mature miRNA region

Extended variants
information (count: 4864 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:4864 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572324013	chr2:180629419-180629420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs62180387	chr2:180629422-180629423	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs13017621	chr2:180629451-180629452	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs62180388	chr2:180629511-180629512	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs547546899	chr2:180629512-180629513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533376154	chr2:180629580-180629581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150908576	chr2:180629590-180629591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369255805	chr2:180629591-180629592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558431701	chr2:180629631-180629632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575178481	chr2:180629659-180629660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs62180389	chr2:180629688-180629689	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs563121453	chr2:180629752-180629753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574322536	chr2:180629775-180629776	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140996113	chr2:180629778-180629779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540336551	chr2:180629797-180629798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139427255	chr2:180629879-180629880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577514258	chr2:180629959-180629960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149660242	chr2:180629963-180629964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs114385698	chr2:180629977-180629978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113008649	chr2:180630023-180630024	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35635820	chr2:180630103-180630104	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563219341	chr2:180630115-180630116	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532029638	chr2:180630127-180630128	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76508191	chr2:180630176-180630177	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113512063	chr2:180630186-180630187	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369113394	chr2:180630258-180630259	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192292793	chr2:180630271-180630272	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565672639	chr2:180630274-180630275	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547880283	chr2:180630309-180630310	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77728190	chr2:180630317-180630318	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538493579	chr2:180630347-180630348	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183734265	chr2:180630381-180630382	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10182519	chr2:180630391-180630392	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs188719453	chr2:180630411-180630412	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368161794	chr2:180630419-180630420	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554532842	chr2:180630467-180630468	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548156525	chr2:180630539-180630540	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574381562	chr2:180630586-180630587	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533505525	chr2:180630634-180630635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553952794	chr2:180630657-180630658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577005560	chr2:180630658-180630659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546456281	chr2:180630708-180630709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs357686	chr2:180630724-180630725	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs192968852	chr2:180630753-180630754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142193227	chr2:180630757-180630758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370506061	chr2:180630758-180630759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183573879	chr2:180630786-180630787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187341838	chr2:180630792-180630793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs71029829	chr2:180630793-180630794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs16866984	chr2:180630846-180630847	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:49)

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
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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:836 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180623600-180630200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:180624200-180629600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:180625400-180630000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr2:180629400-180631200	Weak transcription	Liver	Liver
5	chr2:180629600-180630600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:180629600-180633200	Weak transcription	Stomach Smooth Muscle	stomach
7	chr2:180630000-180630200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr2:180630000-180630800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr2:180630000-180631200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr2:180630000-180631200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr2:180630000-180631800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr2:180630000-180632200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr2:180630000-180632200	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr2:180630200-180631000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr2:180630200-180631200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr2:180630200-180632200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr2:180630400-180631000	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr2:180630600-180631600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:180630800-180631800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr2:180630800-180633400	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr2:180631000-180632000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr2:180631000-180633200	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr2:180631200-180632200	Strong transcription	Liver	Liver
24	chr2:180631600-180632000	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:180631600-180632200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:180631800-180632000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr2:180632000-180632200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr2:180632000-180633400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr2:180632200-180633200	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr2:180632200-180634000	Weak transcription	Liver	Liver
31	chr2:180633200-180633400	Enhancers	Fetal Heart	heart
32	chr2:180633200-180633400	Enhancers	Fetal Thymus	thymus
33	chr2:180633200-180633600	Enhancers	Colon Smooth Muscle	Colon
34	chr2:180633200-180633600	Enhancers	K562	blood
35	chr2:180633200-180634200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr2:180633200-180634400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr2:180633200-180634400	Enhancers	Fetal Stomach	stomach
38	chr2:180633200-180634400	Enhancers	Stomach Smooth Muscle	stomach
39	chr2:180633200-180635000	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr2:180633400-180633600	Enhancers	H1 Cell Line	embryonic stem cell
41	chr2:180633400-180633600	Enhancers	Brain Hippocampus Middle	brain
42	chr2:180633400-180633600	Flanking Active TSS	Fetal Heart	heart
43	chr2:180633400-180633800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr2:180633400-180633800	Enhancers	Fetal Lung	lung
45	chr2:180633400-180634000	Enhancers	Rectal Smooth Muscle	rectum
46	chr2:180633400-180634200	Enhancers	Osteobl	bone
47	chr2:180633400-180634600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:180633400-180635000	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr2:180633600-180633800	Enhancers	Fetal Heart	heart
50	chr2:180633600-180634000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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