Variant report

Variant	esv1813823
Chromosome Location	chr2:127417657-127441005
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:390)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:390 , 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	chr2:127431270-127432113	K562	blood:	n/a	n/a
2	ATF2	chr2:127421667-127422215	GM12878	blood:	n/a	n/a
3	BACH1	chr2:127424089-127424167	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr2:127434513-127435247	GM12878	blood:	n/a	n/a
5	BCL3	chr2:127419353-127419748	GM12878	blood:	n/a	n/a
6	BCL3	chr2:127434589-127435177	GM12878	blood:	n/a	n/a
7	BCL3	chr2:127419319-127419733	GM12878	blood:	n/a	n/a
8	BCL3	chr2:127431489-127432150	K562	blood:	n/a	chr2:127431799-127431806 chr2:127431761-127431768 chr2:127432056-127432069
9	BHLHE40	chr2:127421753-127422394	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:127420454-127420471	K562	blood:	n/a	n/a
11	BHLHE40	chr2:127434883-127434932	K562	blood:	n/a	n/a
12	BHLHE40	chr2:127419483-127419608	K562	blood:	n/a	n/a
13	BHLHE40	chr2:127431316-127431977	K562	blood:	n/a	n/a
14	BHLHE40	chr2:127421937-127421989	K562	blood:	n/a	n/a
15	BRCA1	chr2:127434746-127434749	GM12878	blood:	n/a	n/a
16	CBX3	chr2:127433109-127433587	K562	blood:	n/a	n/a
17	CBX3	chr2:127431212-127432602	K562	blood:	n/a	n/a
18	CBX3	chr2:127432901-127433637	K562	blood:	n/a	n/a
19	CBX3	chr2:127434326-127434831	K562	blood:	n/a	n/a
20	CBX3	chr2:127431600-127431982	K562	blood:	n/a	n/a
21	CCNT2	chr2:127431572-127432099	K562	blood:	n/a	chr2:127431796-127431816
22	CEBPB	chr2:127427463-127427579	A549	lung:	n/a	chr2:127427482-127427493
23	CEBPB	chr2:127419006-127419093	K562	blood:	n/a	n/a
24	CEBPB	chr2:127427442-127427534	IMR90	lung:	n/a	chr2:127427482-127427493
25	CEBPB	chr2:127426042-127426046	K562	blood:	n/a	n/a
26	CEBPB	chr2:127431566-127431956	K562	blood:	n/a	n/a
27	CEBPB	chr2:127427335-127427633	K562	blood:	n/a	chr2:127427482-127427493
28	CEBPB	chr2:127427459-127427573	HepG2	liver:	n/a	chr2:127427482-127427493
29	CEBPB	chr2:127439244-127439415	K562	blood:	n/a	n/a
30	CEBPD	chr2:127431478-127432102	K562	blood:	n/a	n/a
31	CEBPD	chr2:127431465-127432099	K562	blood:	n/a	n/a
32	CHD1	chr2:127421561-127422110	GM12878	blood:	n/a	n/a
33	CHD2	chr2:127419512-127419628	GM12878	blood:	n/a	n/a
34	CHD2	chr2:127431522-127431995	K562	blood:	n/a	n/a
35	CHD2	chr2:127421749-127422413	GM12878	blood:	n/a	n/a
36	CREB1	chr2:127431461-127432093	K562	blood:	n/a	n/a
37	CTCF	chr2:127422000-127422150	GM12865	blood:	n/a	n/a
38	CTCF	chr2:127440960-127441110	GM12869	blood:	n/a	n/a
39	CTCF	chr2:127432081-127432212	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:127421933-127422205	GM12878	blood:	n/a	n/a
41	CTCF	chr2:127440920-127441070	GM12872	blood:	n/a	n/a
42	CTCF	chr2:127440840-127440990	AG10803	skin:	n/a	n/a
43	CTCF	chr2:127418600-127418750	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr2:127440920-127441070	HVMF	connective:	n/a	n/a
45	CTCF	chr2:127440900-127441050	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr2:127440880-127441030	GM12871	blood:	n/a	n/a
47	CTCF	chr2:127440940-127441090	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr2:127431846-127432362	K562	blood:	n/a	n/a
49	CTCF	chr2:127440920-127441070	K562	blood:	n/a	n/a
50	CTCF	chr2:127431757-127432329	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:127426516-127426566	H1-hESC	embryonic stem cell:	embryo
2	chr2:127426516-127426566	NHDF-neo	bronchial:	n/a
3	chr2:127426516-127426566	HIPEpiC	eye:	n/a
4	chr2:127426516-127426566	SKMC	muscle:	n/a
5	chr2:127426516-127426566	NH-A	brain:	n/a
6	chr2:127426516-127426566	PrEC	prostate:	n/a
7	chr2:127426516-127426566	GM19239	blood:	n/a
8	chr2:127426516-127426566	SK-N-MC	brain:	n/a
9	chr2:127426516-127426566	HEK293	kidney:	embryo
10	chr2:127426516-127426566	HCF	heart:	n/a
11	chr2:127426516-127426566	ProgFib	skin:	n/a
12	chr2:127426516-127426566	HL-60	blood:	n/a
13	chr2:127426516-127426566	BE2_C	brain:	n/a
14	chr2:127426516-127426566	IMR90	lung:	fetal
15	chr2:127426516-127426566	HepG2	liver:	n/a
16	chr2:127426516-127426566	PFSK-1	brain:	n/a
17	chr2:127426516-127426566	NHBE	bronchial:	n/a
18	chr2:127426516-127426566	HCPEpiC	choroid plexus:	n/a
19	chr2:127426516-127426566	SK-N-SH	brain:	n/a
20	chr2:127426516-127426566	AoSMC	blood vessel:	n/a
21	chr2:127426516-127426566	AG10803	skin:	n/a
22	chr2:127426516-127426566	HRPEpiC	eye:	n/a
23	chr2:127426516-127426566	HMEC	breast:	n/a
24	chr2:127426516-127426566	HEEpiC	esophagus:	n/a
25	chr2:127426516-127426566	K562	blood:	n/a
26	chr2:127426516-127426566	HNPCEpiC	eye:	n/a
27	chr2:127426516-127426566	ovcar-3	ovarian:	n/a
28	chr2:127426516-127426566	MCF10A-Er-Src	breast:	n/a
29	chr2:127426516-127426566	HUVEC	blood vessel:	n/a
30	chr2:127426516-127426566	AG04450	lung:	fetal
31	chr2:127426516-127426566	HRCEpiC	kidney:	n/a
32	chr2:127426516-127426566	BJ	skin:	n/a
33	chr2:127426516-127426566	HAEpiC	amniotic membrane:	n/a
34	chr2:127426516-127426566	HPAEpiC	pulmonary alveolar:	n/a
35	chr2:127426516-127426566	GM12892	blood:	n/a
36	chr2:127426516-127426566	NB4	blood:	n/a
37	chr2:127426516-127426566	NT2-D1	testis:	n/a
38	chr2:127426516-127426566	Caco-2	colon:	n/a
39	chr2:127426516-127426566	GM12878	blood:	n/a
40	chr2:127426516-127426566	ECC-1	luminal epithelium:	n/a
41	chr2:127426516-127426566	AG04449	skin:	fetal
42	chr2:127426516-127426566	RPTEC	kidney:	n/a
43	chr2:127426516-127426566	A549	lung:	n/a
44	chr2:127426516-127426566	PANC-1	pancreas:	n/a
45	chr2:127426516-127426566	AG09309	skin:	n/a
46	chr2:127426516-127426566	U87	brain:	n/a
47	chr2:127426516-127426566	Hepatocyte	liver:	n/a
48	chr2:127426516-127426566	SAEC	small airway:	n/a
49	chr2:127426516-127426566	GM06990	blood:	n/a
50	chr2:127426516-127426566	HCT-116	colon:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:127440013..127442980-chr2:127454337..127456567,2	K562	blood:
2	chr2:127426020..127428369-chr2:127431324..127434102,4	K562	blood:
3	chr2:127430614..127433355-chr2:127436468..127438269,2	K562	blood:
4	chr2:127430614..127434258-chr2:127435312..127438269,3	K562	blood:
5	chr2:127434663..127437638-chr2:127440272..127442975,3	K562	blood:
6	chr2:127426536..127429355-chr2:127441115..127443378,3	K562	blood:
7	chr2:127433698..127435508-chr2:127441094..127442678,2	K562	blood:
8	chr2:127434549..127436811-chr2:127437779..127440229,2	K562	blood:
9	chr2:127434549..127436811-chr2:127437779..127440229,2	K562	blood:
10	chr2:127437217..127440041-chr2:127447833..127449448,2	K562	blood:
11	chr2:127421256..127423531-chr2:127529484..127531021,2	K562	blood:
12	chr2:127423618..127425430-chr2:127436236..127438617,2	MCF-7	breast:
13	chr2:127430249..127432742-chr2:127444629..127446893,2	K562	blood:
14	chr2:127426020..127428369-chr2:127431324..127434102,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC114783.1.1-5	chr2:127437198-127437996	NONHSAT074134
2	lnc-AC114783.1.1-6	chr2:127435877-127436463	NONHSAT074133

No data

Variant related genes	Relation type
ENSG00000235128	TF binding region
ENSG00000235128	CpG island
ENSG00000235128	chromatin interactions

Extended variants
information (count: 1045 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1045 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575163364	chr2:127417718-127417719	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs190900497	chr2:127417725-127417726	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs544005812	chr2:127417808-127417809	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs561061742	chr2:127417821-127417822	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs28369972	chr2:127417822-127417823	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs574162053	chr2:127417895-127417896	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs573151074	chr2:127417900-127417901	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs559868153	chr2:127417910-127417911	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs144319699	chr2:127417920-127417921	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs552437793	chr2:127417929-127417930	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs180803609	chr2:127417942-127417943	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs530911882	chr2:127417948-127417949	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs550670131	chr2:127417963-127417964	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs540564597	chr2:127417986-127417987	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs28387094	chr2:127417987-127417988	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs564582614	chr2:127417994-127417995	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs147711604	chr2:127418011-127418012	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs567064677	chr2:127418014-127418015	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs539000283	chr2:127418076-127418077	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs550297182	chr2:127418077-127418078	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs569907653	chr2:127418116-127418117	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs559184523	chr2:127418140-127418141	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs77514386	chr2:127418173-127418174	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs562029943	chr2:127418183-127418184	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs537864290	chr2:127418205-127418206	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs375496316	chr2:127418213-127418214	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs574198827	chr2:127418214-127418215	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs118100270	chr2:127418263-127418264	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs142564007	chr2:127418296-127418297	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs186196031	chr2:127418325-127418326	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs549037008	chr2:127418340-127418341	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs576612780	chr2:127418400-127418401	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs545806625	chr2:127418453-127418454	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs28387095	chr2:127418459-127418460	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs531470565	chr2:127418462-127418463	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs191019027	chr2:127418502-127418503	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs561217867	chr2:127418555-127418556	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs530261977	chr2:127418559-127418560	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs117790872	chr2:127418598-127418599	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs558981975	chr2:127418706-127418707	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs575932155	chr2:127418731-127418732	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs372670492	chr2:127418732-127418733	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs146902343	chr2:127418733-127418734	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs539244703	chr2:127418794-127418795	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs552462207	chr2:127418835-127418836	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs7574360	chr2:127418837-127418838	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs145891209	chr2:127418840-127418841	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs554190428	chr2:127418932-127418933	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs567709075	chr2:127418960-127418961	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs542731114	chr2:127418991-127418992	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	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
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
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Mental retardation	17621639	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Medulloblastoma	16968546	CNVD
Neurocytoma	17123091	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:997 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:127415000-127417800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:127415000-127417800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:127415000-127423200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr2:127415200-127417800	Weak transcription	Brain Germinal Matrix	brain
5	chr2:127415200-127428000	Weak transcription	Gastric	stomach
6	chr2:127415400-127417800	Enhancers	Pancreas	Pancrea
7	chr2:127415400-127418400	Weak transcription	Brain Hippocampus Middle	brain
8	chr2:127415400-127419600	Enhancers	Esophagus	oesophagus
9	chr2:127415600-127417800	Transcr. at gene 5' and 3'	K562	blood
10	chr2:127415600-127418800	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
11	chr2:127415600-127421000	Enhancers	Left Ventricle	heart
12	chr2:127415600-127422800	Enhancers	Right Atrium	heart
13	chr2:127415600-127423200	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr2:127415600-127424600	Enhancers	Right Ventricle	heart
15	chr2:127416000-127417800	Enhancers	HSMM	muscle
16	chr2:127416000-127421400	Weak transcription	Liver	Liver
17	chr2:127416000-127422600	Genic enhancers	Fetal Muscle Leg	muscle
18	chr2:127416000-127423600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr2:127416200-127417800	Enhancers	Colonic Mucosa	Colon
20	chr2:127416200-127417800	Enhancers	Fetal Lung	lung
21	chr2:127416200-127417800	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr2:127416200-127418600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr2:127416200-127418600	Enhancers	Colon Smooth Muscle	Colon
24	chr2:127416200-127419400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr2:127416200-127429000	Weak transcription	Fetal Intestine Small	intestine
26	chr2:127416200-127430000	Weak transcription	Fetal Intestine Large	intestine
27	chr2:127416200-127430200	Weak transcription	Aorta	Aorta
28	chr2:127416600-127417800	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr2:127416600-127420400	Enhancers	Ovary	ovary
30	chr2:127416600-127425000	Enhancers	Fetal Heart	heart
31	chr2:127416800-127421800	Enhancers	Primary B cells from cord blood	blood
32	chr2:127416800-127425400	Weak transcription	Small Intestine	intestine
33	chr2:127417000-127418000	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:127417000-127418000	Strong transcription	Fetal Stomach	stomach
35	chr2:127417000-127418000	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr2:127417000-127419000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr2:127417000-127419600	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr2:127417000-127419600	Enhancers	Fetal Thymus	thymus
39	chr2:127417000-127420000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr2:127417000-127421200	Weak transcription	Brain Substantia Nigra	brain
41	chr2:127417000-127421200	Enhancers	Placenta	Placenta
42	chr2:127417000-127421400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr2:127417000-127422400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr2:127417000-127423200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr2:127417000-127423400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr2:127417000-127424000	Enhancers	Psoas Muscle	Psoas
47	chr2:127417200-127417800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:127417200-127417800	Enhancers	Primary T cells fromperipheralblood	blood
49	chr2:127417200-127417800	Enhancers	Thymus	Thymus
50	chr2:127417200-127418000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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