Variant report

Variant	nsv535631
Chromosome Location	chr2:34468037-34738307
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	ATF2	chr2:34492233-34492695	GM12878	blood:	n/a	n/a
2	ATF2	chr2:34590863-34591498	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr2:34626250-34626627	GM12878	blood:	n/a	chr2:34626402-34626412 chr2:34626401-34626412
4	BATF	chr2:34626271-34626588	GM12878	blood:	n/a	chr2:34626402-34626412 chr2:34626401-34626412
5	BATF	chr2:34516235-34516448	GM12878	blood:	n/a	n/a
6	BATF	chr2:34492248-34492667	GM12878	blood:	n/a	chr2:34492484-34492495
7	BATF	chr2:34516238-34516504	GM12878	blood:	n/a	n/a
8	BATF	chr2:34492306-34492669	GM12878	blood:	n/a	chr2:34492484-34492495
9	BCL11A	chr2:34492295-34492624	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:34591088-34591422	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr2:34626351-34626529	GM12878	blood:	n/a	chr2:34626400-34626409 chr2:34626401-34626410
12	BCL3	chr2:34633212-34633509	GM12878	blood:	n/a	chr2:34633318-34633327 chr2:34633317-34633326
13	BCL3	chr2:34633202-34633571	GM12878	blood:	n/a	chr2:34633318-34633327 chr2:34633317-34633326
14	BHLHE40	chr2:34492074-34492695	GM12878	blood:	n/a	n/a
15	BHLHE40	chr2:34633159-34633448	GM12878	blood:	n/a	n/a
16	CCNT2	chr2:34623370-34623530	K562	blood:	n/a	n/a
17	CEBPB	chr2:34706631-34706981	IMR90	lung:	n/a	chr2:34706794-34706805
18	CEBPB	chr2:34637625-34637979	A549	lung:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
19	CEBPB	chr2:34610823-34611180	IMR90	lung:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008
20	CEBPB	chr2:34637693-34638019	A549	lung:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
21	CEBPB	chr2:34610850-34611138	MCF-7	breast:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008
22	CEBPB	chr2:34651815-34652025	H1-hESC	embryonic stem cell:	n/a	chr2:34651953-34651964
23	CEBPB	chr2:34637610-34637983	IMR90	lung:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
24	CEBPB	chr2:34637607-34637980	HepG2	liver:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
25	CEBPB	chr2:34505441-34505585	A549	lung:	n/a	chr2:34505549-34505560 chr2:34505551-34505560 chr2:34505551-34505562
26	CEBPB	chr2:34637636-34637968	Hela-S3	cervix:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
27	CEBPB	chr2:34505394-34505654	HepG2	liver:	n/a	chr2:34505549-34505560 chr2:34505551-34505560 chr2:34505551-34505562
28	CEBPB	chr2:34651784-34652054	A549	lung:	n/a	chr2:34651953-34651964
29	CEBPB	chr2:34637613-34637978	K562	blood:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
30	CEBPB	chr2:34706608-34706989	HepG2	liver:	n/a	chr2:34706794-34706805
31	CEBPB	chr2:34637705-34637966	MCF-7	breast:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
32	CEBPB	chr2:34717914-34718139	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:34517483-34517740	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:34651788-34652080	HepG2	liver:	n/a	chr2:34651953-34651964
35	CEBPB	chr2:34610798-34611191	HepG2	liver:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008
36	CEBPB	chr2:34590884-34591363	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr2:34634613-34634777	A549	lung:	n/a	n/a
38	CEBPB	chr2:34541175-34541372	HepG2	liver:	n/a	chr2:34541344-34541357 chr2:34541346-34541357 chr2:34541341-34541358 chr2:34541344-34541355
39	CEBPB	chr2:34633778-34633979	HepG2	liver:	n/a	chr2:34633880-34633891 chr2:34633878-34633891 chr2:34633878-34633889 chr2:34633878-34633891
40	CEBPB	chr2:34717910-34718155	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr2:34736004-34736033	HepG2	liver:	n/a	chr2:34736017-34736028
42	CEBPB	chr2:34651786-34652048	K562	blood:	n/a	chr2:34651953-34651964
43	CEBPB	chr2:34531788-34532038	A549	lung:	n/a	n/a
44	CEBPB	chr2:34637621-34637979	H1-hESC	embryonic stem cell:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
45	CEBPB	chr2:34512235-34512435	HepG2	liver:	n/a	chr2:34512358-34512369 chr2:34512358-34512371
46	CEBPB	chr2:34637712-34637983	ECC-1	luminal epithelium:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
47	CEBPB	chr2:34651781-34652060	IMR90	lung:	n/a	chr2:34651953-34651964
48	CEBPB	chr2:34637703-34637950	MCF-7	breast:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
49	CEBPB	chr2:34661633-34661923	HepG2	liver:	n/a	chr2:34661857-34661869
50	CEBPB	chr2:34608697-34608972	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:34719719-34719769	GM12892	blood:	n/a
2	chr2:34633637-34633687	GM12892	blood:	n/a
3	chr2:34633637-34633687	CMK	blood:	n/a
4	chr2:34719719-34719769	HEEpiC	esophagus:	n/a
5	chr2:34720275-34720325	HCPEpiC	choroid plexus:	n/a
6	chr2:34720275-34720325	AG10803	skin:	n/a
7	chr2:34633637-34633687	AG04449	skin:	fetal
8	chr2:34633637-34633687	Hepatocyte	liver:	n/a
9	chr2:34590591-34590641	HNPCEpiC	eye:	n/a
10	chr2:34719719-34719769	T-47D	breast:	n/a
11	chr2:34719719-34719769	Hepatocyte	liver:	n/a
12	chr2:34633637-34633687	PrEC	prostate:	n/a
13	chr2:34720275-34720325	SK-N-SH_RA	brain:	n/a
14	chr2:34633637-34633687	AG09309	skin:	n/a
15	chr2:34720275-34720325	GM19239	blood:	n/a
16	chr2:34719565-34719615	SKMC	muscle:	n/a
17	chr2:34719719-34719769	HUVEC	blood vessel:	n/a
18	chr2:34590591-34590641	HCPEpiC	choroid plexus:	n/a
19	chr2:34590591-34590641	HMEC	breast:	n/a
20	chr2:34590591-34590641	GM12878	blood:	n/a
21	chr2:34719565-34719615	SK-N-SH	brain:	n/a
22	chr2:34719719-34719769	CMK	blood:	n/a
23	chr2:34633637-34633687	ECC-1	luminal epithelium:	n/a
24	chr2:34719719-34719769	HNPCEpiC	eye:	n/a
25	chr2:34590591-34590641	GM06990	blood:	n/a
26	chr2:34590591-34590641	NB4	blood:	n/a
27	chr2:34719719-34719769	SAEC	small airway:	n/a
28	chr2:34590591-34590641	MCF-7	breast:	n/a
29	chr2:34719565-34719615	Jurkat	blood:	n/a
30	chr2:34590591-34590641	HepG2	liver:	n/a
31	chr2:34590591-34590641	SK-N-SH	brain:	n/a
32	chr2:34719719-34719769	HPAEpiC	pulmonary alveolar:	n/a
33	chr2:34719565-34719615	HUVEC	blood vessel:	n/a
34	chr2:34719565-34719615	HAEpiC	amniotic membrane:	n/a
35	chr2:34719565-34719615	HCT-116	colon:	n/a
36	chr2:34719565-34719615	NH-A	brain:	n/a
37	chr2:34590591-34590641	AG09319	gingival:	n/a
38	chr2:34720275-34720325	HUVEC	blood vessel:	n/a
39	chr2:34720275-34720325	U87	brain:	n/a
40	chr2:34719565-34719615	HRE	kidney:	n/a
41	chr2:34590591-34590641	GM12891	blood:	n/a
42	chr2:34719719-34719769	BE2_C	brain:	n/a
43	chr2:34719719-34719769	HRCEpiC	kidney:	n/a
44	chr2:34719565-34719615	HMEC	breast:	n/a
45	chr2:34719565-34719615	PFSK-1	brain:	n/a
46	chr2:34719719-34719769	NB4	blood:	n/a
47	chr2:34720275-34720325	NHBE	bronchial:	n/a
48	chr2:34590591-34590641	NT2-D1	testis:	n/a
49	chr2:34719719-34719769	PANC-1	pancreas:	n/a
50	chr2:34590591-34590641	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:41466170..41467868-chr2:34623111..34624611,2	MCF-7	breast:
2	chr2:34590795..34592507-chr2:34600278..34603033,2	K562	blood:
3	chr2:34451708..34454413-chr2:34493747..34495311,2	K562	blood:
4	chr2:34636657..34638446-chr2:34644514..34646250,2	K562	blood:
5	chr2:34469910..34471896-chr2:34475795..34477495,2	MCF-7	breast:
6	chr2:34636657..34638446-chr2:34644514..34646250,2	K562	blood:
7	chr2:34707651..34709954-chr2:34710435..34712219,2	MCF-7	breast:
8	chr2:34469910..34471896-chr2:34475795..34477495,2	MCF-7	breast:
9	chr2:34624209..34626557-chr2:34688886..34690644,2	K562	blood:
10	chr2:34520994..34523413-chr2:34524356..34526580,2	MCF-7	breast:
11	chr2:34590795..34592507-chr2:34600278..34603033,2	K562	blood:
12	chr2:34624209..34626557-chr2:34688886..34690644,2	K562	blood:
13	chr2:34520994..34523413-chr2:34524356..34526580,2	MCF-7	breast:
14	chr2:34707651..34709954-chr2:34710435..34712219,2	MCF-7	breast:
15	chr17:57969237..57970939-chr2:34675539..34678526,2	MCF-7	breast:
16	chr2:34541264..34543781-chr2:34553502..34555371,2	MCF-7	breast:
17	chr2:34541264..34543781-chr2:34553502..34555371,2	MCF-7	breast:
18	chr12:46765173..46767943-chr2:34590937..34593382,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASGRP3-1	chr2:34522535-34522820	ENSG00000203386
2	lnc-RASGRP3-3	chr2:34608855-34609276	ENSG00000226785
3	lnc-RASGRP3-1	chr2:34511710-34511813	ENSG00000203386
4	lnc-RASGRP3-3	chr2:34609584-34609636	ENSG00000226785
5	lnc-RASGRP3-3	chr2:34609584-34609796	NONHSAT070034
6	lnc-RASGRP3-3	chr2:34511701-34511813	NONHSAT070034
7	lnc-RASGRP3-13	chr2:34713820-34713911	NONHSAT070033

Variant related genes	Relation type
ENSG00000212025	TF binding region
ENSG00000226785	TF binding region
ENSG00000212025	CpG island
ENSG00000226785	CpG island
ENSG00000108443	chromatin interactions
ENSG00000258096	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000108423	chromatin interactions

Extended variants
information (count: 5360 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:5360 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558135026	chr2:34468090-34468091	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs148307744	chr2:34468304-34468305	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73927738	chr2:34468378-34468379	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs741557	chr2:34468438-34468439	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs529075005	chr2:34468443-34468444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542888235	chr2:34468487-34468488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192011139	chr2:34468490-34468491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531643772	chr2:34468509-34468510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551063401	chr2:34468525-34468526	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs72782916	chr2:34468539-34468540	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs546242053	chr2:34468565-34468566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112906080	chr2:34468575-34468576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547448569	chr2:34468577-34468578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2005906	chr2:34468642-34468643	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs183276478	chr2:34468657-34468658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555549533	chr2:34468665-34468666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185317541	chr2:34468691-34468692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538551834	chr2:34468741-34468742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144869399	chr2:34468766-34468767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201520348	chr2:34468806-34468807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533612873	chr2:34468811-34468812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553388523	chr2:34468812-34468813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs3072780	chr2:34468832-34468833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372233289	chr2:34468833-34468834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557831928	chr2:34468843-34468844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576263890	chr2:34468870-34468871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577952600	chr2:34468890-34468891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78022065	chr2:34468961-34468962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554301610	chr2:34468968-34468969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189676340	chr2:34468970-34468971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574272025	chr2:34468977-34468978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201902810	chr2:34468978-34468979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200354329	chr2:34468979-34468980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376453280	chr2:34468981-34468982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182810078	chr2:34468986-34468987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576225833	chr2:34469023-34469024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545272925	chr2:34469059-34469060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138321015	chr2:34469083-34469084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527275958	chr2:34469090-34469091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377710974	chr2:34469097-34469098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547031848	chr2:34469140-34469141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147856129	chr2:34469144-34469145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544506560	chr2:34469147-34469148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs741556	chr2:34469155-34469156	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs549136490	chr2:34469169-34469170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569122749	chr2:34469188-34469189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs55861488	chr2:34469189-34469190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374473214	chr2:34469231-34469232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538088476	chr2:34469238-34469239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs72782919	chr2:34469279-34469280	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Incontinentia Pigmenti	22033527	CNVD
Alcoholism	22295116	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:34465600-34468400	Enhancers	Ovary	ovary
2	chr2:34466400-34468200	Enhancers	Pancreas	Pancrea
3	chr2:34466400-34468400	Enhancers	Fetal Lung	lung
4	chr2:34466400-34468600	Enhancers	Fetal Brain Male	brain
5	chr2:34466600-34468600	Enhancers	Liver	Liver
6	chr2:34467000-34468200	Enhancers	Brain Germinal Matrix	brain
7	chr2:34467000-34468600	Enhancers	Fetal Intestine Large	intestine
8	chr2:34467000-34468600	Enhancers	Fetal Intestine Small	intestine
9	chr2:34467000-34468600	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr2:34467200-34468200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
11	chr2:34467200-34468400	Enhancers	Duodenum Mucosa	Duodenum
12	chr2:34467400-34468200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr2:34467400-34475600	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr2:34467600-34469200	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr2:34468000-34468200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr2:34468000-34468200	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr2:34468000-34468400	Flanking Active TSS	Fetal Kidney	kidney
18	chr2:34468200-34479200	Weak transcription	Pancreas	Pancrea
19	chr2:34468400-34477200	Weak transcription	Fetal Lung	lung
20	chr2:34468600-34474600	Weak transcription	Fetal Intestine Small	intestine
21	chr2:34468600-34474600	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr2:34469200-34469400	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr2:34469400-34469600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr2:34469400-34469600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:34470800-34471800	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr2:34471800-34472200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr2:34472200-34472400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr2:34472200-34473000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr2:34472600-34472800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr2:34472800-34473200	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr2:34473200-34479200	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr2:34474400-34474600	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr2:34474600-34474800	Enhancers	Fetal Intestine Small	intestine
34	chr2:34474600-34474800	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr2:34474600-34477600	Enhancers	Fetal Intestine Large	intestine
36	chr2:34474800-34475400	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr2:34474800-34475400	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr2:34474800-34475600	Weak transcription	Fetal Intestine Small	intestine
39	chr2:34475400-34475600	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr2:34475600-34476000	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr2:34475600-34476400	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr2:34475600-34480800	Enhancers	Fetal Intestine Small	intestine
43	chr2:34476000-34477000	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr2:34476400-34477600	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr2:34476600-34476800	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr2:34477000-34477400	Enhancers	Rectal Mucosa Donor 29	rectum
47	chr2:34477200-34477600	Enhancers	Fetal Lung	lung
48	chr2:34477600-34478400	Weak transcription	Fetal Intestine Large	intestine
49	chr2:34477600-34478400	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr2:34477600-34479400	Weak transcription	Fetal Lung	lung

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