Variant report

Variant	nsv874792
Chromosome Location	chr2:110732676-110871665
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1624)
CpG islands
(count:368)
Chromatin interactive
region (count:18)
LncRNA
region (count:8)
Mature miRNA
region (count: 3)
miRNA target
sites (count:0)

(count:1624 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:110859522-110859666	HepG2	liver:	n/a	n/a
2	ATF3	chr2:110858656-110859426	A549	lung:	n/a	n/a
3	ATF3	chr2:110858605-110859874	A549	lung:	n/a	n/a
4	ATF3	chr2:110863340-110864704	A549	lung:	n/a	n/a
5	ATF3	chr2:110863282-110864651	A549	lung:	n/a	n/a
6	BATF	chr2:110829579-110829796	GM12878	blood:	n/a	n/a
7	BATF	chr2:110738365-110738645	GM12878	blood:	n/a	n/a
8	BATF	chr2:110733954-110734198	GM12878	blood:	n/a	n/a
9	BATF	chr2:110859621-110859879	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:110738261-110738582	GM12878	blood:	n/a	n/a
11	BCL3	chr2:110861855-110862496	A549	lung:	n/a	n/a
12	BCL3	chr2:110858630-110860176	A549	lung:	n/a	chr2:110859557-110859566 chr2:110859688-110859697 chr2:110859202-110859211
13	BCL3	chr2:110863085-110865362	A549	lung:	n/a	chr2:110863098-110863107
14	BCL3	chr2:110871334-110872613	A549	lung:	n/a	n/a
15	BCL3	chr2:110863087-110865215	A549	lung:	n/a	chr2:110863098-110863107
16	BCL3	chr2:110858636-110860316	A549	lung:	n/a	chr2:110859557-110859566 chr2:110859688-110859697 chr2:110859202-110859211
17	BCL3	chr2:110871502-110872812	A549	lung:	n/a	n/a
18	BCL3	chr2:110861718-110862627	A549	lung:	n/a	n/a
19	BHLHE40	chr2:110829505-110829790	HepG2	liver:	n/a	n/a
20	BHLHE40	chr2:110858908-110858916	K562	blood:	n/a	n/a
21	BHLHE40	chr2:110745383-110745582	HepG2	liver:	n/a	n/a
22	BHLHE40	chr2:110871580-110872256	HepG2	liver:	n/a	n/a
23	BHLHE40	chr2:110858774-110859754	A549	lung:	n/a	n/a
24	BHLHE40	chr2:110863718-110864150	A549	lung:	n/a	n/a
25	BHLHE40	chr2:110863741-110864010	HepG2	liver:	n/a	n/a
26	BRCA1	chr2:110863081-110864069	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr2:110858725-110859542	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr2:110738340-110738572	K562	blood:	n/a	n/a
29	CEBPB	chr2:110863164-110864849	HCT-116	colon:	n/a	n/a
30	CEBPB	chr2:110863522-110864600	A549	lung:	n/a	n/a
31	CEBPB	chr2:110810802-110811002	A549	lung:	n/a	chr2:110810876-110810887
32	CEBPB	chr2:110864241-110864498	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:110863325-110864836	A549	lung:	n/a	n/a
34	CEBPB	chr2:110858979-110859462	A549	lung:	n/a	n/a
35	CEBPB	chr2:110861712-110862302	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr2:110810820-110811025	HepG2	liver:	n/a	chr2:110810876-110810887
37	CEBPB	chr2:110863350-110864062	MCF-7	breast:	n/a	n/a
38	CEBPB	chr2:110864244-110864588	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:110870081-110870415	A549	lung:	n/a	n/a
40	CEBPB	chr2:110858873-110859809	A549	lung:	n/a	n/a
41	CEBPB	chr2:110858731-110859782	A549	lung:	n/a	n/a
42	CEBPB	chr2:110810829-110810999	Hela-S3	cervix:	n/a	chr2:110810876-110810887
43	CEBPB	chr2:110852762-110853042	IMR90	lung:	n/a	chr2:110852900-110852913
44	CEBPB	chr2:110864143-110864674	A549	lung:	n/a	n/a
45	CEBPB	chr2:110858740-110859579	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr2:110863557-110864104	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr2:110757218-110757426	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr2:110863610-110864043	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr2:110863396-110864118	A549	lung:	n/a	n/a
50	CEBPB	chr2:110810834-110810990	K562	blood:	n/a	chr2:110810876-110810887

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:110871644-110871694	U87	brain:	n/a
2	chr2:110827645-110827695	GM06990	blood:	n/a
3	chr2:110871644-110871694	U87	brain:	n/a
4	chr2:110827645-110827695	GM06990	blood:	n/a
5	chr2:110827645-110827695	HRE	kidney:	n/a
6	chr2:110871644-110871694	GM06990	blood:	n/a
7	chr2:110871644-110871694	GM12878	blood:	n/a
8	chr2:110859091-110859141	NT2-D1	testis:	n/a
9	chr2:110871644-110871694	PFSK-1	brain:	n/a
10	chr2:110829661-110829711	SK-N-SH	brain:	n/a
11	chr2:110833739-110833789	GM12892	blood:	n/a
12	chr2:110859091-110859141	NH-A	brain:	n/a
13	chr2:110871644-110871694	AG04450	lung:	fetal
14	chr2:110863886-110863936	HUVEC	blood vessel:	n/a
15	chr2:110833739-110833789	HCT-116	colon:	n/a
16	chr2:110829661-110829711	T-47D	breast:	n/a
17	chr2:110833739-110833789	MCF10A-Er-Src	breast:	n/a
18	chr2:110863886-110863936	ProgFib	skin:	n/a
19	chr2:110863886-110863936	A549	lung:	n/a
20	chr2:110827645-110827695	SK-N-MC	brain:	n/a
21	chr2:110829661-110829711	BJ	skin:	n/a
22	chr2:110827645-110827695	AoSMC	blood vessel:	n/a
23	chr2:110829661-110829711	ECC-1	luminal epithelium:	n/a
24	chr2:110827645-110827695	GM19239	blood:	n/a
25	chr2:110859091-110859141	AG09309	skin:	n/a
26	chr2:110833739-110833789	HepG2	liver:	n/a
27	chr2:110859091-110859141	Jurkat	blood:	n/a
28	chr2:110859091-110859141	AoSMC	blood vessel:	n/a
29	chr2:110829661-110829711	HRPEpiC	eye:	n/a
30	chr2:110871644-110871694	HNPCEpiC	eye:	n/a
31	chr2:110827645-110827695	T-47D	breast:	n/a
32	chr2:110827645-110827695	PANC-1	pancreas:	n/a
33	chr2:110863886-110863936	HEEpiC	esophagus:	n/a
34	chr2:110863886-110863936	HCF	heart:	n/a
35	chr2:110833739-110833789	ECC-1	luminal epithelium:	n/a
36	chr2:110827645-110827695	ECC-1	luminal epithelium:	n/a
37	chr2:110871644-110871694	IMR90	lung:	fetal
38	chr2:110829661-110829711	Jurkat	blood:	n/a
39	chr2:110833739-110833789	GM12878	blood:	n/a
40	chr2:110833739-110833789	SAEC	small airway:	n/a
41	chr2:110829661-110829711	HRE	kidney:	n/a
42	chr2:110863886-110863936	NT2-D1	testis:	n/a
43	chr2:110871644-110871694	HMEC	breast:	n/a
44	chr2:110863886-110863936	BE2_C	brain:	n/a
45	chr2:110863886-110863936	AG10803	skin:	n/a
46	chr2:110829661-110829711	BE2_C	brain:	n/a
47	chr2:110859091-110859141	GM12891	blood:	n/a
48	chr2:110829661-110829711	HPAEpiC	pulmonary alveolar:	n/a
49	chr2:110827645-110827695	PFSK-1	brain:	n/a
50	chr2:110863886-110863936	Jurkat	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:110858332..110860187-chr2:110869577..110871663,2	MCF-7	breast:
2	chr2:110857583..110859746-chr2:110914068..110916196,2	MCF-7	breast:
3	chr2:110855266..110858639-chr2:110858645..110861501,3	MCF-7	breast:
4	chr2:110859259..110860018-chr7:26239929..26240470,2	Hela-S3	cervix:
5	chr2:110857860..110860963-chr2:110860996..110866153,6	MCF-7	breast:
6	chr2:110862148..110865580-chr2:110871176..110875147,4	MCF-7	breast:
7	chr2:110855266..110858639-chr2:110858645..110861501,3	MCF-7	breast:
8	chr2:110871483..110872172-chr2:110914465..110915379,4	MCF-7	breast:
9	chr2:110863346..110864881-chr2:110906381..110908081,2	MCF-7	breast:
10	chr2:110863205..110865655-chr2:110910127..110912316,2	MCF-7	breast:
11	chr2:110855709..110858865-chr2:110862093..110865475,3	MCF-7	breast:
12	chr2:110855709..110858865-chr2:110862093..110865475,3	MCF-7	breast:
13	chr2:110859680..110861955-chr2:110862122..110864189,2	MCF-7	breast:
14	chr2:110864486..110867223-chr2:110872239..110874303,2	MCF-7	breast:
15	chr2:110859680..110861955-chr2:110862122..110864189,2	MCF-7	breast:
16	chr2:110859324..110861924-chr2:110871252..110875012,4	MCF-7	breast:
17	chr2:110858332..110860187-chr2:110869577..110871663,2	MCF-7	breast:
18	chr2:110857860..110860963-chr2:110860996..110866153,6	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LIMS3-1	chr2:110751978-110753717	ENSG00000204588
2	lnc-LIMS3-1	chr2:110746130-110746278	NONHSAT073165
3	lnc-LIMS3-1	chr2:110744703-110744767	NONHSAT073165
4	lnc-LIMS3-1	chr2:110751978-110752031	NONHSAT073165
5	lnc-LIMS3-1	chr2:110746317-110746379	NONHSAT073165
6	lnc-MALL-3	chr2:110769842-110770178	NONHSAT073169
7	lnc-LIMS3-1	chr2:110745138-110745187	NONHSAT073165
8	lnc-LIMS3-1	chr2:110745849-110746379	ENSG00000204588

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4436b-3p	chr2:110844020-110844041	MIMAT0019941
hsa-miR-4436b-5p	chr2:110844067-110844088	MIMAT0019940
hsa-miR-4267	chr2:110827594-110827609	MIMAT0016893

No data

Variant related genes	Relation type
ENSG00000229730	TF binding region
LINC01123	TF binding region
MIR4436B1	TF binding region
MIR4267	TF binding region
ZBTB45P1	TF binding region
ENSG00000235721	TF binding region
GPAA1P1	TF binding region
ENSG00000229730	CpG island
LINC01123	CpG island
MIR4436B1	CpG island
MIR4267	CpG island
ZBTB45P1	CpG island
ENSG00000235721	CpG island
GPAA1P1	CpG island
ENSG00000144063	chromatin interactions
ENSG00000122566	chromatin interactions

Extended variants
information (count: 1089 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1089 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540625662	chr2:110738259-110738260	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs336701	chr2:110738305-110738306	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs369269722	chr2:110738327-110738328	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs560727210	chr2:110738391-110738392	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs529603276	chr2:110738494-110738495	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs549743418	chr2:110738737-110738738	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs185889550	chr2:110738774-110738775	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs531964331	chr2:110738777-110738778	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs199500468	chr2:110738798-110738799	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs550367611	chr2:110738812-110738813	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs367985110	chr2:110738843-110738844	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs538696574	chr2:110738844-110738845	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs539014538	chr2:110738899-110738900	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs546569449	chr2:110738931-110738932	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs2124961	chr2:110739130-110739131	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs563189274	chr2:110739678-110739679	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs571399457	chr2:110742211-110742212	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs339196	chr2:110742626-110742627	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs373152667	chr2:110743667-110743668	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs336709	chr2:110743690-110743691	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs533992791	chr2:110743774-110743775	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs554277122	chr2:110743814-110743815	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs565138343	chr2:110743840-110743841	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs200875767	chr2:110743841-110743842	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs388398	chr2:110743852-110743853	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs142252171	chr2:110743856-110743857	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs62159145	chr2:110744420-110744421	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs377420291	chr2:110745996-110745997	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs188552360	chr2:110746170-110746171	Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs539306421	chr2:110746193-110746194	Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs67932826	chr2:110746204-110746205	Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs572573222	chr2:110746240-110746241	Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs542732988	chr2:110746576-110746577	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs370823008	chr2:110749174-110749175	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs559776662	chr2:110749659-110749660	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs376647021	chr2:110749833-110749834	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs567909426	chr2:110750038-110750039	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs564090933	chr2:110750041-110750042	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs371148779	chr2:110752474-110752475	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs374410466	chr2:110752547-110752548	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs542359240	chr2:110752772-110752773	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs368759779	chr2:110752774-110752775	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs371117761	chr2:110752796-110752797	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs373637784	chr2:110752797-110752798	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs336708	chr2:110752828-110752829	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs367775221	chr2:110752837-110752838	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs78186126	chr2:110752838-110752839	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs201575560	chr2:110752859-110752860	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs562481253	chr2:110752877-110752878	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs368197526	chr2:110752879-110752880	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Disease	19212409	CNVD

Chromatin state (count:561 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:110746000-110746400	Active TSS	Fetal Intestine Small	intestine
2	chr2:110757400-110757600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr2:110783800-110784000	Enhancers	Fetal Intestine Large	intestine
4	chr2:110783800-110786000	Weak transcription	Pancreas	Pancrea
5	chr2:110785800-110792600	Weak transcription	Fetal Intestine Large	intestine
6	chr2:110786000-110786400	Enhancers	Fetal Muscle Trunk	muscle
7	chr2:110792600-110793000	Enhancers	Pancreas	Pancrea
8	chr2:110805800-110806600	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr2:110805800-110806600	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr2:110806000-110806600	Enhancers	Pancreas	Pancrea
11	chr2:110806000-110807600	Enhancers	Fetal Muscle Trunk	muscle
12	chr2:110806000-110807600	Enhancers	HepG2	liver
13	chr2:110806200-110806600	Enhancers	HSMMtube	muscle
14	chr2:110806400-110807000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr2:110810400-110811000	Enhancers	HUVEC	blood vessel
16	chr2:110810600-110810800	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr2:110810600-110810800	Enhancers	Fetal Heart	heart
18	chr2:110810600-110810800	Enhancers	A549	lung
19	chr2:110810600-110810800	Enhancers	NHEK	skin
20	chr2:110810600-110811000	Enhancers	Fetal Lung	lung
21	chr2:110810600-110811000	Enhancers	Dnd41	blood
22	chr2:110811000-110812000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr2:110811000-110812000	Weak transcription	Fetal Heart	heart
24	chr2:110811000-110812000	Weak transcription	Fetal Lung	lung
25	chr2:110811000-110812000	Weak transcription	A549	lung
26	chr2:110811000-110812000	Weak transcription	HUVEC	blood vessel
27	chr2:110811000-110812000	Weak transcription	NHEK	skin
28	chr2:110812000-110812200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr2:110812000-110812200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr2:110812000-110812200	Enhancers	Fetal Brain Male	brain
31	chr2:110812000-110812200	Enhancers	Fetal Lung	lung
32	chr2:110812000-110812400	Enhancers	H1 Cell Line	embryonic stem cell
33	chr2:110812000-110812400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr2:110812000-110812400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr2:110812000-110812400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:110812000-110812400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:110812000-110812400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr2:110812000-110812400	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr2:110812000-110812400	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr2:110812000-110812400	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr2:110812000-110812400	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr2:110812000-110812400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr2:110812000-110812400	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr2:110812000-110812400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr2:110812000-110812400	Enhancers	Brain Hippocampus Middle	brain
46	chr2:110812000-110812400	Enhancers	Fetal Heart	heart
47	chr2:110812000-110812400	Enhancers	Fetal Intestine Large	intestine
48	chr2:110812000-110812400	Enhancers	Fetal Intestine Small	intestine
49	chr2:110812000-110812400	Enhancers	Fetal Stomach	stomach
50	chr2:110812000-110812400	Enhancers	Left Ventricle	heart

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