Variant report

Variant	nsv874785
Chromosome Location	chr2:110524250-110843108
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2826)
CpG islands
(count:305)
Chromatin interactive
region (count:0)
LncRNA
region (count:13)
Mature miRNA
region (count: 1)
miRNA target
sites (count:3)

(count:2826 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr2:110555685-110555899	GM12878	blood:	n/a	n/a
2	BATF	chr2:110596658-110596861	GM12878	blood:	n/a	n/a
3	BATF	chr2:110645383-110645632	GM12878	blood:	n/a	n/a
4	BATF	chr2:110550261-110550597	GM12878	blood:	n/a	n/a
5	BATF	chr2:110554721-110555155	GM12878	blood:	n/a	n/a
6	BATF	chr2:110663352-110663813	GM12878	blood:	n/a	chr2:110663553-110663564 chr2:110663608-110663619
7	BATF	chr2:110628682-110629136	GM12878	blood:	n/a	n/a
8	BATF	chr2:110653035-110653493	GM12878	blood:	n/a	n/a
9	BATF	chr2:110738365-110738645	GM12878	blood:	n/a	n/a
10	BATF	chr2:110554663-110555199	GM12878	blood:	n/a	n/a
11	BATF	chr2:110653717-110654248	GM12878	blood:	n/a	chr2:110654054-110654064 chr2:110654053-110654064
12	BATF	chr2:110551684-110552114	GM12878	blood:	n/a	n/a
13	BATF	chr2:110596705-110596958	GM12878	blood:	n/a	n/a
14	BATF	chr2:110655074-110655448	GM12878	blood:	n/a	n/a
15	BATF	chr2:110662784-110663052	GM12878	blood:	n/a	chr2:110662929-110662940
16	BATF	chr2:110597287-110597588	GM12878	blood:	n/a	n/a
17	BATF	chr2:110594892-110595317	GM12878	blood:	n/a	n/a
18	BATF	chr2:110663321-110663821	GM12878	blood:	n/a	chr2:110663553-110663564 chr2:110663608-110663619
19	BATF	chr2:110591595-110591865	GM12878	blood:	n/a	n/a
20	BATF	chr2:110733954-110734198	GM12878	blood:	n/a	n/a
21	BATF	chr2:110552518-110552811	GM12878	blood:	n/a	n/a
22	BATF	chr2:110565195-110565489	GM12878	blood:	n/a	n/a
23	BATF	chr2:110829579-110829796	GM12878	blood:	n/a	n/a
24	BATF	chr2:110592910-110593154	GM12878	blood:	n/a	n/a
25	BATF	chr2:110645180-110645680	GM12878	blood:	n/a	n/a
26	BATF	chr2:110653650-110654385	GM12878	blood:	n/a	chr2:110654054-110654064 chr2:110654053-110654064
27	BATF	chr2:110595079-110595276	GM12878	blood:	n/a	n/a
28	BATF	chr2:110628689-110629008	GM12878	blood:	n/a	n/a
29	BCL11A	chr2:110552372-110552860	GM12878	blood:	n/a	chr2:110552563-110552572
30	BCL11A	chr2:110738261-110738582	GM12878	blood:	n/a	n/a
31	BCL11A	chr2:110667539-110667813	GM12878	blood:	n/a	n/a
32	BCL11A	chr2:110550280-110550534	GM12878	blood:	n/a	n/a
33	BCL11A	chr2:110599243-110599681	GM12878	blood:	n/a	n/a
34	BCL11A	chr2:110622746-110622931	GM12878	blood:	n/a	n/a
35	BCL11A	chr2:110659894-110660095	GM12878	blood:	n/a	chr2:110659948-110659957
36	BCL11A	chr2:110663268-110663851	GM12878	blood:	n/a	n/a
37	BCL11A	chr2:110552529-110552917	GM12878	blood:	n/a	chr2:110552563-110552572
38	BCL11A	chr2:110554748-110555164	GM12878	blood:	n/a	n/a
39	BCL11A	chr2:110653155-110653347	GM12878	blood:	n/a	n/a
40	BCL11A	chr2:110653775-110654123	GM12878	blood:	n/a	n/a
41	BCL11A	chr2:110608683-110608858	GM12878	blood:	n/a	n/a
42	BCL11A	chr2:110653735-110654258	GM12878	blood:	n/a	n/a
43	BCL11A	chr2:110663316-110663738	GM12878	blood:	n/a	n/a
44	BCL11A	chr2:110555695-110555957	GM12878	blood:	n/a	n/a
45	BCL11A	chr2:110615296-110615523	GM12878	blood:	n/a	n/a
46	BCL11A	chr2:110551708-110552101	GM12878	blood:	n/a	n/a
47	BCL11A	chr2:110584727-110584955	GM12878	blood:	n/a	n/a
48	BCL11A	chr2:110653076-110653477	GM12878	blood:	n/a	n/a
49	BCL11A	chr2:110602022-110602295	GM12878	blood:	n/a	n/a
50	BCL11A	chr2:110628740-110628913	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:110706159-110706209	HIPEpiC	eye:	n/a
2	chr2:110833739-110833789	ProgFib	skin:	n/a
3	chr2:110706159-110706209	NH-A	brain:	n/a
4	chr2:110827645-110827695	AG04450	lung:	fetal
5	chr2:110827645-110827695	NHBE	bronchial:	n/a
6	chr2:110827645-110827695	ProgFib	skin:	n/a
7	chr2:110706159-110706209	PANC-1	pancreas:	n/a
8	chr2:110705781-110705831	HAEpiC	amniotic membrane:	n/a
9	chr2:110706159-110706209	AoSMC	blood vessel:	n/a
10	chr2:110833739-110833789	SAEC	small airway:	n/a
11	chr2:110827645-110827695	HCF	heart:	n/a
12	chr2:110705781-110705831	Caco-2	colon:	n/a
13	chr2:110827645-110827695	NB4	blood:	n/a
14	chr2:110829661-110829711	CMK	blood:	n/a
15	chr2:110705781-110705831	PFSK-1	brain:	n/a
16	chr2:110706159-110706209	ovcar-3	ovarian:	n/a
17	chr2:110827645-110827695	ovcar-3	ovarian:	n/a
18	chr2:110829661-110829711	ovcar-3	ovarian:	n/a
19	chr2:110705781-110705831	HPAEpiC	pulmonary alveolar:	n/a
20	chr2:110833739-110833789	HAEpiC	amniotic membrane:	n/a
21	chr2:110827645-110827695	CMK	blood:	n/a
22	chr2:110833739-110833789	H1-hESC	embryonic stem cell:	embryo
23	chr2:110705781-110705831	K562	blood:	n/a
24	chr2:110829661-110829711	NH-A	brain:	n/a
25	chr2:110827645-110827695	K562	blood:	n/a
26	chr2:110829661-110829711	K562	blood:	n/a
27	chr2:110833739-110833789	Jurkat	blood:	n/a
28	chr2:110829661-110829711	SK-N-SH_RA	brain:	n/a
29	chr2:110827645-110827695	HRCEpiC	kidney:	n/a
30	chr2:110706159-110706209	PFSK-1	brain:	n/a
31	chr2:110706159-110706209	HCPEpiC	choroid plexus:	n/a
32	chr2:110705781-110705831	A549	lung:	n/a
33	chr2:110705781-110705831	AG04449	skin:	fetal
34	chr2:110706159-110706209	BJ	skin:	n/a
35	chr2:110706159-110706209	AG09319	gingival:	n/a
36	chr2:110833739-110833789	HCPEpiC	choroid plexus:	n/a
37	chr2:110706159-110706209	AG04449	skin:	fetal
38	chr2:110829661-110829711	A549	lung:	n/a
39	chr2:110829661-110829711	LNCaP	prostate:	n/a
40	chr2:110829661-110829711	PANC-1	pancreas:	n/a
41	chr2:110833739-110833789	SK-N-MC	brain:	n/a
42	chr2:110705781-110705831	HMEC	breast:	n/a
43	chr2:110706159-110706209	NHBE	bronchial:	n/a
44	chr2:110705781-110705831	HRPEpiC	eye:	n/a
45	chr2:110827645-110827695	HRE	kidney:	n/a
46	chr2:110706159-110706209	U87	brain:	n/a
47	chr2:110706159-110706209	HEEpiC	esophagus:	n/a
48	chr2:110706159-110706209	BE2_C	brain:	n/a
49	chr2:110829661-110829711	AG04450	lung:	fetal
50	chr2:110705781-110705831	MCF-7	breast:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LIMS3-1	chr2:110746317-110746379	NONHSAT073165
2	lnc-LIMS3-1	chr2:110744703-110744767	NONHSAT073165
3	lnc-LIMS3-1	chr2:110746130-110746278	NONHSAT073165
4	lnc-LIMS3-1	chr2:110751978-110752031	NONHSAT073165
5	lnc-SEPT10-2	chr2:110615775-110615987	ucscGeneNc_uc010fjz_1
6	lnc-MALL-3	chr2:110769842-110770178	NONHSAT073169
7	lnc-LIMS3.1-2	chr2:110595460-110595619	NONHSAT073153
8	lnc-LIMS3-1	chr2:110751978-110753717	ENSG00000204588
9	lnc-SEPT10-2	chr2:110595035-110595535	ucscGeneNc_uc010fjz_1
10	lnc-LIMS3.1-2	chr2:110596511-110596570	NONHSAT073153
11	lnc-SEPT10-2	chr2:110598802-110598916	ucscGeneNc_uc010fjz_1
12	lnc-LIMS3-1	chr2:110745849-110746379	ENSG00000204588
13	lnc-LIMS3-1	chr2:110745138-110745187	NONHSAT073165

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4267	chr2:110827594-110827609	MIMAT0016893

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RGPD5	hsa-miR-335-5p	chr2:110614364-110614387
2	RGPD6	hsa-miR-15a-5p	chr2:110615252-110615272
3	RGPD6	hsa-miR-15a-5p	chr2:110614843-110614864

Variant related genes	Relation type
ENSG00000235721	TF binding region
ENSG00000229730	TF binding region
GPAA1P1	TF binding region
LINC01123	TF binding region
ENSG00000186148	TF binding region
LIMS3	TF binding region
RGPD5	TF binding region
MIR4267	TF binding region
ZBTB45P1	TF binding region
ENSG00000235721	CpG island
ENSG00000229730	CpG island
GPAA1P1	CpG island
LINC01123	CpG island
ENSG00000186148	CpG island
LIMS3	CpG island
RGPD5	CpG island
MIR4267	CpG island
ZBTB45P1	CpG island

Extended variants
information (count: 340 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62151741	chr2:110551101-110551102	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs28478863	chr2:110552127-110552128	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs574513766	chr2:110552180-110552181	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs543726285	chr2:110552181-110552182	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs368194978	chr2:110552185-110552186	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs372016063	chr2:110556568-110556569	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs10191102	chr2:110556714-110556715	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs112178381	chr2:110564671-110564672	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs2918665	chr2:110572702-110572703	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs28589309	chr2:110572744-110572745	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs2918664	chr2:110572752-110572753	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs150007575	chr2:110572888-110572889	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs2438862	chr2:110572971-110572972	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs111968970	chr2:110574953-110574954	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs2673122	chr2:110574954-110574955	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs62163513	chr2:110591985-110591986	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs55711961	chr2:110595885-110595886	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs62161350	chr2:110651914-110651915	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs62161352	chr2:110652608-110652609	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs62161353	chr2:110652617-110652618	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs62161354	chr2:110653592-110653593	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs62161355	chr2:110653661-110653662	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs62161356	chr2:110653663-110653664	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs62161357	chr2:110653709-110653710	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs113406090	chr2:110654079-110654080	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs3806526	chr2:110655896-110655897	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs62162963	chr2:110656623-110656624	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs62159067	chr2:110685770-110685771	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs78658664	chr2:110685934-110685935	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs336803	chr2:110694251-110694252	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs1966906	chr2:110694378-110694379	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs540625662	chr2:110738259-110738260	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs336701	chr2:110738305-110738306	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs369269722	chr2:110738327-110738328	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs560727210	chr2:110738391-110738392	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs529603276	chr2:110738494-110738495	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs549743418	chr2:110738737-110738738	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs185889550	chr2:110738774-110738775	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs531964331	chr2:110738777-110738778	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs199500468	chr2:110738798-110738799	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs550367611	chr2:110738812-110738813	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs367985110	chr2:110738843-110738844	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs538696574	chr2:110738844-110738845	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs539014538	chr2:110738899-110738900	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs546569449	chr2:110738931-110738932	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs2124961	chr2:110739130-110739131	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs563189274	chr2:110739678-110739679	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs571399457	chr2:110742211-110742212	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs339196	chr2:110742626-110742627	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs373152667	chr2:110743667-110743668	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
Autism	22549408	CNVD
Autism	21865298	CNVD
small cell lung cancer	20016488	CNVD
Disease	19212409	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:110552000-110552400	Active TSS	H1 Cell Line	embryonic stem cell
2	chr2:110552000-110552400	Active TSS	H9 Cell Line	embryonic stem cell
3	chr2:110552000-110552400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:110552000-110552400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:110552000-110552400	Active TSS	Cortex derived primary cultured neurospheres	brain
6	chr2:110552000-110552400	Active TSS	Left Ventricle	heart
7	chr2:110552000-110552400	Active TSS	Ovary	ovary
8	chr2:110552000-110552400	Active TSS	Psoas Muscle	Psoas
9	chr2:110552000-110552400	Active TSS	Right Atrium	heart
10	chr2:110552000-110552400	Active TSS	Right Ventricle	heart
11	chr2:110552000-110552400	Active TSS	Thymus	Thymus
12	chr2:110552000-110552400	Active TSS	HMEC	breast
13	chr2:110552000-110552400	Active TSS	HSMM	muscle
14	chr2:110746000-110746400	Active TSS	Fetal Intestine Small	intestine
15	chr2:110757400-110757600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr2:110783800-110784000	Enhancers	Fetal Intestine Large	intestine
17	chr2:110783800-110786000	Weak transcription	Pancreas	Pancrea
18	chr2:110785800-110792600	Weak transcription	Fetal Intestine Large	intestine
19	chr2:110786000-110786400	Enhancers	Fetal Muscle Trunk	muscle
20	chr2:110792600-110793000	Enhancers	Pancreas	Pancrea
21	chr2:110805800-110806600	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr2:110805800-110806600	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr2:110806000-110806600	Enhancers	Pancreas	Pancrea
24	chr2:110806000-110807600	Enhancers	Fetal Muscle Trunk	muscle
25	chr2:110806000-110807600	Enhancers	HepG2	liver
26	chr2:110806200-110806600	Enhancers	HSMMtube	muscle
27	chr2:110806400-110807000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr2:110810400-110811000	Enhancers	HUVEC	blood vessel
29	chr2:110810600-110810800	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr2:110810600-110810800	Enhancers	Fetal Heart	heart
31	chr2:110810600-110810800	Enhancers	A549	lung
32	chr2:110810600-110810800	Enhancers	NHEK	skin
33	chr2:110810600-110811000	Enhancers	Fetal Lung	lung
34	chr2:110810600-110811000	Enhancers	Dnd41	blood
35	chr2:110811000-110812000	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr2:110811000-110812000	Weak transcription	Fetal Heart	heart
37	chr2:110811000-110812000	Weak transcription	Fetal Lung	lung
38	chr2:110811000-110812000	Weak transcription	A549	lung
39	chr2:110811000-110812000	Weak transcription	HUVEC	blood vessel
40	chr2:110811000-110812000	Weak transcription	NHEK	skin
41	chr2:110812000-110812200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr2:110812000-110812200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr2:110812000-110812200	Enhancers	Fetal Brain Male	brain
44	chr2:110812000-110812200	Enhancers	Fetal Lung	lung
45	chr2:110812000-110812400	Enhancers	H1 Cell Line	embryonic stem cell
46	chr2:110812000-110812400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr2:110812000-110812400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr2:110812000-110812400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:110812000-110812400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:110812000-110812400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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