Variant report

Variant	nsv2874
Chromosome Location	chr2:110289373-110333621
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:648)
CpG islands
(count:61)
Chromatin interactive
region (count:24)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:648 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:110315840-110316481	HepG2	liver:	n/a	chr2:110316153-110316169
2	ARID3A	chr2:110295405-110295698	HepG2	liver:	n/a	n/a
3	ATF1	chr2:110332183-110332280	K562	blood:	n/a	n/a
4	ATF1	chr2:110316161-110316375	K562	blood:	n/a	n/a
5	BACH1	chr2:110316076-110316457	H1-hESC	embryonic stem cell:	n/a	chr2:110316237-110316251
6	BATF	chr2:110303694-110303989	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:110318618-110318814	K562	blood:	n/a	n/a
8	BHLHE40	chr2:110303673-110304338	GM12878	blood:	n/a	n/a
9	BRCA1	chr2:110303768-110304108	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr2:110323217-110323255	GM12878	blood:	n/a	n/a
11	CBX3	chr2:110316109-110316524	HCT-116	colon:	n/a	n/a
12	CBX3	chr2:110316016-110316627	HCT-116	colon:	n/a	n/a
13	CEBPB	chr2:110315906-110316624	HCT-116	colon:	n/a	n/a
14	CEBPB	chr2:110316145-110316543	MCF-7	breast:	n/a	n/a
15	CEBPB	chr2:110316159-110316500	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:110316194-110316456	K562	blood:	n/a	n/a
17	CEBPB	chr2:110319933-110320356	A549	lung:	n/a	n/a
18	CEBPB	chr2:110320035-110320337	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:110319830-110320488	HCT-116	colon:	n/a	n/a
20	CEBPB	chr2:110316107-110316423	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:110316011-110316543	A549	lung:	n/a	n/a
22	CEBPB	chr2:110316091-110316468	A549	lung:	n/a	n/a
23	CEBPB	chr2:110316139-110316513	A549	lung:	n/a	n/a
24	CEBPB	chr2:110303715-110304017	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr2:110315947-110316485	HCT-116	colon:	n/a	n/a
26	CEBPB	chr2:110316157-110316528	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:110316145-110316530	IMR90	lung:	n/a	n/a
28	CEBPB	chr2:110316170-110316443	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:110320038-110320369	A549	lung:	n/a	n/a
30	CEBPB	chr2:110319904-110320377	A549	lung:	n/a	n/a
31	CEBPB	chr2:110326118-110326245	HepG2	liver:	n/a	chr2:110326154-110326167
32	CEBPB	chr2:110316157-110316500	K562	blood:	n/a	n/a
33	CEBPB	chr2:110316136-110316534	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr2:110316125-110316559	MCF-7	breast:	n/a	n/a
35	CHD2	chr2:110328501-110328710	K562	blood:	n/a	n/a
36	CHD2	chr2:110299281-110299388	GM12878	blood:	n/a	n/a
37	CHD2	chr2:110316148-110316448	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr2:110303719-110304005	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr2:110303820-110303970	AG04450	lung:	n/a	n/a
40	CTCF	chr2:110303704-110304012	A549	lung:	n/a	n/a
41	CTCF	chr2:110303671-110304030	A549	lung:	n/a	n/a
42	CTCF	chr2:110298940-110299090	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr2:110303760-110303910	GM12878	blood:	n/a	n/a
44	CTCF	chr2:110303800-110303950	HRE	kidney:	n/a	n/a
45	CTCF	chr2:110303633-110304034	A549	lung:	n/a	n/a
46	CTCF	chr2:110303820-110303970	HCFaa	heart:	n/a	n/a
47	CTCF	chr2:110303600-110303750	HCM	heart:	n/a	n/a
48	CTCF	chr2:110303719-110303988	MCF-7	breast:	n/a	n/a
49	CTCF	chr2:110303760-110303910	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr2:110303800-110303950	GM12873	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:110317956-110318006	GM12892	blood:	n/a
2	chr2:110317956-110318006	AG09309	skin:	n/a
3	chr2:110317956-110318006	H1-hESC	embryonic stem cell:	embryo
4	chr2:110317956-110318006	HIPEpiC	eye:	n/a
5	chr2:110317956-110318006	PrEC	prostate:	n/a
6	chr2:110317956-110318006	HRE	kidney:	n/a
7	chr2:110317956-110318006	RPTEC	kidney:	n/a
8	chr2:110317956-110318006	K562	blood:	n/a
9	chr2:110317956-110318006	ovcar-3	ovarian:	n/a
10	chr2:110317956-110318006	HCPEpiC	choroid plexus:	n/a
11	chr2:110317956-110318006	MCF-7	breast:	n/a
12	chr2:110317956-110318006	HNPCEpiC	eye:	n/a
13	chr2:110317956-110318006	SKMC	muscle:	n/a
14	chr2:110317956-110318006	HRPEpiC	eye:	n/a
15	chr2:110317956-110318006	T-47D	breast:	n/a
16	chr2:110317956-110318006	PANC-1	pancreas:	n/a
17	chr2:110317956-110318006	SK-N-MC	brain:	n/a
18	chr2:110317956-110318006	NH-A	brain:	n/a
19	chr2:110317956-110318006	NHBE	bronchial:	n/a
20	chr2:110317956-110318006	AG10803	skin:	n/a
21	chr2:110317956-110318006	AG04449	skin:	fetal
22	chr2:110317956-110318006	GM19239	blood:	n/a
23	chr2:110317956-110318006	IMR90	lung:	fetal
24	chr2:110317956-110318006	GM12891	blood:	n/a
25	chr2:110317956-110318006	A549	lung:	n/a
26	chr2:110317956-110318006	HAEpiC	amniotic membrane:	n/a
27	chr2:110317956-110318006	HUVEC	blood vessel:	n/a
28	chr2:110317956-110318006	SK-N-SH	brain:	n/a
29	chr2:110317956-110318006	Hela-S3	cervix:	n/a
30	chr2:110317956-110318006	Jurkat	blood:	n/a
31	chr2:110317956-110318006	HEEpiC	esophagus:	n/a
32	chr2:110317956-110318006	NT2-D1	testis:	n/a
33	chr2:110317956-110318006	HCT-116	colon:	n/a
34	chr2:110317956-110318006	PFSK-1	brain:	n/a
35	chr2:110317956-110318006	Caco-2	colon:	n/a
36	chr2:110317956-110318006	AoSMC	blood vessel:	n/a
37	chr2:110317956-110318006	ProgFib	skin:	n/a
38	chr2:110317956-110318006	HCF	heart:	n/a
39	chr2:110317956-110318006	HEK293	kidney:	embryo
40	chr2:110317956-110318006	HL-60	blood:	n/a
41	chr2:110317956-110318006	NB4	blood:	n/a
42	chr2:110317956-110318006	U87	brain:	n/a
43	chr2:110317956-110318006	GM06990	blood:	n/a
44	chr2:110317956-110318006	MCF10A-Er-Src	breast:	n/a
45	chr2:110317956-110318006	LNCaP	prostate:	n/a
46	chr2:110317956-110318006	SK-N-SH_RA	brain:	n/a
47	chr2:110317956-110318006	ECC-1	luminal epithelium:	n/a
48	chr2:110317956-110318006	BJ	skin:	n/a
49	chr2:110317956-110318006	HRCEpiC	kidney:	n/a
50	chr2:110317956-110318006	HPAEpiC	pulmonary alveolar:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:110314274..110316891-chr2:110317469..110319541,2	K562	blood:
2	chr2:110303139..110304334-chr2:110493545..110494430,6	MCF-7	breast:
3	chr2:110266262..110268417-chr2:110288079..110290936,2	K562	blood:
4	chr2:110295767..110297906-chr2:110298255..110300414,3	K562	blood:
5	chr2:110273684..110274551-chr2:110303700..110304336,2	MCF-7	breast:
6	chr2:110303406..110303961-chr2:110421277..110421785,2	MCF-7	breast:
7	chr2:110306100..110309560-chr2:110371773..110373561,3	MCF-7	breast:
8	chr2:110310683..110312314-chr2:110314864..110316411,2	MCF-7	breast:
9	chr2:110315553..110317822-chr2:110320975..110322550,2	MCF-7	breast:
10	chr2:110295767..110297372-chr2:110298255..110300414,2	K562	blood:
11	chr2:110303649..110304318-chr2:110493558..110494245,2	K562	blood:
12	chr2:110295767..110297906-chr2:110298255..110300414,3	K562	blood:
13	chr2:110303360..110304330-chr2:110420115..110421127,10	MCF-7	breast:
14	chr2:110310683..110312314-chr2:110314864..110316411,2	MCF-7	breast:
15	chr2:110303351..110304315-chr2:110420246..110421095,4	MCF-7	breast:
16	chr2:110315553..110317822-chr2:110320975..110322550,2	MCF-7	breast:
17	chr2:110314274..110316891-chr2:110317469..110319541,2	K562	blood:
18	chr2:110315967..110317938-chr2:110370785..110372677,2	MCF-7	breast:
19	chr2:110295767..110297372-chr2:110298255..110300414,2	K562	blood:
20	chr2:110273676..110274668-chr2:110298391..110299091,2	K562	blood:
21	chr2:110316867..110319657-chr2:110370281..110372107,2	MCF-7	breast:
22	chr2:110321272..110323476-chr2:110330973..110332963,2	MCF-7	breast:
23	chr2:110287242..110289237-chr2:110289566..110292595,3	MCF-7	breast:
24	chr2:110321272..110323476-chr2:110330973..110332963,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MALL-6	chr2:110329652-110329823	l_1917_NR_027063
2	lnc-MALL-6	chr2:110331530-110331629	l_1917_NR_027063
3	lnc-MALL-6	chr2:110327081-110327741	l_1917_NR_027063
4	lnc-MALL-6	chr2:110326395-110326488	l_1917_NR_027063
5	lnc-SH3RF3-2	chr2:110310113-110310423	NONHSAT073143
6	lnc-MALL-6	chr2:110332525-110332654	l_1917_NR_027063
7	lnc-MALL-6	chr2:110326395-110326488	NONHSAT073144
8	lnc-MALL-6	chr2:110329651-110329823	NONHSAT073144
9	lnc-MALL-6	chr2:110327081-110327741	NONHSAT073144
10	lnc-MALL-6	chr2:110331530-110331629	NONHSAT073144
11	lnc-MALL-6	chr2:110330543-110330673	NONHSAT073144
12	lnc-MALL-6	chr2:110332525-110332654	NONHSAT073144
13	lnc-MALL-6	chr2:110330543-110330673	l_1917_NR_027063

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SEPT10	hsa-miR-192-5p	chr2:110300408-110300429
2	SEPT10	hsa-miR-215-5p	chr2:110300408-110300429

Variant related genes	Relation type
SEPT10	TF binding region
ENSG00000237916	TF binding region
SEPT10	CpG island
ENSG00000237916	CpG island
ENSG00000186522	chromatin interactions
ENSG00000198142	chromatin interactions

Extended variants
information (count: 1723 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1723 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545103053	chr2:110289419-110289420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138624083	chr2:110289452-110289453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564931887	chr2:110289533-110289534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555064213	chr2:110289586-110289587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541223264	chr2:110289614-110289615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561207879	chr2:110289619-110289620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571747823	chr2:110289621-110289622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549936351	chr2:110289641-110289642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563724458	chr2:110289778-110289779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534327147	chr2:110289784-110289785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146712309	chr2:110289821-110289822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs116564661	chr2:110289840-110289841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140368080	chr2:110289884-110289885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372744168	chr2:110289885-110289886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534925329	chr2:110289928-110289929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34519997	chr2:110289954-110289955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs9330320	chr2:110289984-110289985	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs373214104	chr2:110290053-110290054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528771536	chr2:110290094-110290095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77409098	chr2:110290118-110290119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139723862	chr2:110290140-110290141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376151579	chr2:110290142-110290143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9330321	chr2:110290160-110290161	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs115345877	chr2:110290187-110290188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575996720	chr2:110290265-110290266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538209211	chr2:110290333-110290334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558732443	chr2:110290357-110290358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563534922	chr2:110290368-110290369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs9798179	chr2:110290381-110290382	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs561043663	chr2:110290414-110290415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs574520680	chr2:110290424-110290425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs188016629	chr2:110290446-110290447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs576464314	chr2:110290507-110290508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532544103	chr2:110290550-110290551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552153285	chr2:110290558-110290559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs559451603	chr2:110290571-110290572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543156610	chr2:110290761-110290762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528540643	chr2:110290775-110290776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192444304	chr2:110290785-110290786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568651732	chr2:110290793-110290794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559776850	chr2:110290829-110290830	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs183720034	chr2:110290880-110290881	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs528446305	chr2:110290904-110290905	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs113959993	chr2:110290924-110290925	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs538668185	chr2:110290986-110290987	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs558571926	chr2:110291058-110291059	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs3923006	chr2:110291087-110291088	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs111800848	chr2:110291101-110291102	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs562312843	chr2:110291107-110291108	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs534731193	chr2:110291108-110291109	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Autism	22495311	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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
lymphocytic leukemia	21291569	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
Autism	22495309	CNVD
Bipolar disorder	19214233	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
Williams Syndrome	20824207	CNVD
Autism	22549408	CNVD
Autism	21865298	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1007 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:110274000-110292800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:110280600-110290600	Weak transcription	Fetal Kidney	kidney
3	chr2:110281000-110292800	Weak transcription	Spleen	Spleen
4	chr2:110285000-110299200	Weak transcription	Aorta	Aorta
5	chr2:110287200-110293200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:110288000-110292600	Weak transcription	Right Ventricle	heart
7	chr2:110288000-110293200	Weak transcription	Ovary	ovary
8	chr2:110288000-110299000	Weak transcription	Esophagus	oesophagus
9	chr2:110288600-110293000	Weak transcription	Gastric	stomach
10	chr2:110288800-110292600	Weak transcription	Right Atrium	heart
11	chr2:110288800-110292800	Weak transcription	Placenta	Placenta
12	chr2:110288800-110293000	Weak transcription	Lung	lung
13	chr2:110289200-110292400	Weak transcription	Fetal Heart	heart
14	chr2:110290200-110291000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr2:110290400-110291400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr2:110290600-110291400	Enhancers	Fetal Kidney	kidney
17	chr2:110290600-110291800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:110290600-110293400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr2:110290800-110291000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr2:110290800-110291400	Bivalent Enhancer	HepG2	liver
21	chr2:110291000-110309400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr2:110291400-110291800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr2:110291400-110295800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr2:110291400-110295800	Weak transcription	Fetal Kidney	kidney
25	chr2:110291600-110291800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr2:110291600-110292800	Bivalent Enhancer	HepG2	liver
27	chr2:110291800-110309400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr2:110292400-110293000	Enhancers	Fetal Heart	heart
29	chr2:110292400-110293400	Enhancers	Pancreas	Pancrea
30	chr2:110292400-110296400	Enhancers	HSMMtube	muscle
31	chr2:110292600-110293200	Enhancers	Fetal Lung	lung
32	chr2:110292600-110293400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr2:110292600-110293400	Enhancers	Right Atrium	heart
34	chr2:110292600-110293400	Enhancers	Right Ventricle	heart
35	chr2:110292600-110293400	Enhancers	HSMM	muscle
36	chr2:110292800-110293000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr2:110292800-110293000	Enhancers	Spleen	Spleen
38	chr2:110292800-110293200	Enhancers	Placenta	Placenta
39	chr2:110292800-110293200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
40	chr2:110292800-110293200	Flanking Bivalent TSS/Enh	HepG2	liver
41	chr2:110292800-110293400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr2:110292800-110293400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr2:110292800-110293400	Enhancers	Fetal Muscle Leg	muscle
44	chr2:110292800-110293400	Enhancers	NHDF-Ad	bronchial
45	chr2:110292800-110293400	Enhancers	NHLF	lung
46	chr2:110292800-110293600	Enhancers	Fetal Intestine Small	intestine
47	chr2:110293000-110293200	Enhancers	Fetal Muscle Trunk	muscle
48	chr2:110293000-110293200	Enhancers	Placenta Amnion	Placenta Amnion
49	chr2:110293000-110293400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr2:110293000-110293400	Enhancers	iPS-20b Cell Line	embryonic stem cell

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