Variant report

Variant	nsv963711
Chromosome Location	chr2:114358889-114381866
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1194)
CpG islands
(count:671)
Chromatin interactive
region (count:5)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1194 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:114367604-114367630	K562	blood:	n/a	n/a
2	ARID3A	chr2:114361646-114361961	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:114360929-114361189	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:114361677-114361888	K562	blood:	n/a	n/a
5	ATF1	chr2:114367425-114367625	K562	blood:	n/a	n/a
6	ATF1	chr2:114361242-114361940	K562	blood:	n/a	n/a
7	ATF2	chr2:114361567-114361900	GM12878	blood:	n/a	n/a
8	ATF2	chr2:114361453-114361981	GM12878	blood:	n/a	n/a
9	ATF3	chr2:114361611-114361934	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr2:114359623-114359862	GM12878	blood:	n/a	n/a
11	ATF3	chr2:114361262-114361840	A549	lung:	n/a	n/a
12	ATF3	chr2:114361178-114361912	HepG2	liver:	n/a	n/a
13	ATF3	chr2:114361199-114361999	K562	blood:	n/a	n/a
14	ATF3	chr2:114361244-114361527	GM12878	blood:	n/a	n/a
15	ATF3	chr2:114359628-114359819	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr2:114359657-114359767	GM12878	blood:	n/a	n/a
17	ATF3	chr2:114361120-114361577	HepG2	liver:	n/a	n/a
18	ATF3	chr2:114361562-114362008	A549	lung:	n/a	n/a
19	ATF3	chr2:114361184-114362015	GM12878	blood:	n/a	n/a
20	ATF3	chr2:114359653-114359828	K562	blood:	n/a	n/a
21	ATF3	chr2:114361598-114361885	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr2:114361596-114362020	HepG2	liver:	n/a	n/a
23	BATF	chr2:114359584-114359759	GM12878	blood:	n/a	n/a
24	BATF	chr2:114359080-114359259	GM12878	blood:	n/a	n/a
25	BATF	chr2:114381240-114381532	GM12878	blood:	n/a	n/a
26	BATF	chr2:114363533-114363803	GM12878	blood:	n/a	n/a
27	BATF	chr2:114361970-114362553	GM12878	blood:	n/a	n/a
28	BATF	chr2:114381555-114381747	GM12878	blood:	n/a	n/a
29	BATF	chr2:114371894-114372100	GM12878	blood:	n/a	n/a
30	BATF	chr2:114366018-114366205	GM12878	blood:	n/a	n/a
31	BATF	chr2:114367221-114367484	GM12878	blood:	n/a	n/a
32	BATF	chr2:114363680-114363884	GM12878	blood:	n/a	n/a
33	BATF	chr2:114370957-114371184	GM12878	blood:	n/a	n/a
34	BATF	chr2:114366912-114367587	GM12878	blood:	n/a	n/a
35	BATF	chr2:114362909-114363236	GM12878	blood:	n/a	n/a
36	BATF	chr2:114361478-114362107	GM12878	blood:	n/a	n/a
37	BATF	chr2:114359457-114359883	GM12878	blood:	n/a	n/a
38	BATF	chr2:114358733-114359308	GM12878	blood:	n/a	n/a
39	BCL11A	chr2:114361535-114362539	GM12878	blood:	n/a	n/a
40	BCL11A	chr2:114381108-114381508	GM12878	blood:	n/a	n/a
41	BCL11A	chr2:114358372-114359354	GM12878	blood:	n/a	n/a
42	BCL11A	chr2:114377588-114377832	GM12878	blood:	n/a	n/a
43	BCL11A	chr2:114359458-114359824	GM12878	blood:	n/a	n/a
44	BCL11A	chr2:114381251-114381571	GM12878	blood:	n/a	n/a
45	BCL11A	chr2:114361489-114362197	GM12878	blood:	n/a	n/a
46	BCL11A	chr2:114362979-114363180	GM12878	blood:	n/a	n/a
47	BCL11A	chr2:114358969-114359373	GM12878	blood:	n/a	n/a
48	BCL11A	chr2:114362360-114362601	GM12878	blood:	n/a	n/a
49	BCL11A	chr2:114361056-114361325	GM12878	blood:	n/a	n/a
50	BCL11A	chr2:114378501-114378802	GM12878	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:114359188-114359238	HepG2	liver:	n/a
2	chr2:114359188-114359238	Hela-S3	cervix:	n/a
3	chr2:114359188-114359238	HL-60	blood:	n/a
4	chr2:114359736-114359786	HRE	kidney:	n/a
5	chr2:114359873-114359923	HEEpiC	esophagus:	n/a
6	chr2:114361816-114361866	HCM	heart:	n/a
7	chr2:114361124-114361174	NHDF-neo	bronchial:	n/a
8	chr2:114359188-114359238	HCT-116	colon:	n/a
9	chr2:114361925-114361975	MCF-7	breast:	n/a
10	chr2:114361162-114361212	HRPEpiC	eye:	n/a
11	chr2:114359762-114359812	GM12892	blood:	n/a
12	chr2:114359251-114359301	NHDF-neo	bronchial:	n/a
13	chr2:114361124-114361174	ProgFib	skin:	n/a
14	chr2:114359188-114359238	AG10803	skin:	n/a
15	chr2:114359762-114359812	LNCaP	prostate:	n/a
16	chr2:114359762-114359812	HMEC	breast:	n/a
17	chr2:114361124-114361174	Caco-2	colon:	n/a
18	chr2:114360096-114360146	K562	blood:	n/a
19	chr2:114361162-114361212	HCM	heart:	n/a
20	chr2:114359188-114359238	BJ	skin:	n/a
21	chr2:114359873-114359923	U87	brain:	n/a
22	chr2:114359188-114359238	HIPEpiC	eye:	n/a
23	chr2:114361124-114361174	BE2_C	brain:	n/a
24	chr2:114362443-114362493	HCF	heart:	n/a
25	chr2:114361124-114361174	ovcar-3	ovarian:	n/a
26	chr2:114360096-114360146	PANC-1	pancreas:	n/a
27	chr2:114361816-114361866	Hepatocyte	liver:	n/a
28	chr2:114361816-114361866	ECC-1	luminal epithelium:	n/a
29	chr2:114360096-114360146	HepG2	liver:	n/a
30	chr2:114361162-114361212	RPTEC	kidney:	n/a
31	chr2:114362443-114362493	SK-N-SH	brain:	n/a
32	chr2:114361162-114361212	BE2_C	brain:	n/a
33	chr2:114362443-114362493	GM12891	blood:	n/a
34	chr2:114362443-114362493	MCF10A-Er-Src	breast:	n/a
35	chr2:114360096-114360146	NB4	blood:	n/a
36	chr2:114359251-114359301	HRE	kidney:	n/a
37	chr2:114361816-114361866	ovcar-3	ovarian:	n/a
38	chr2:114361816-114361866	HEEpiC	esophagus:	n/a
39	chr2:114361124-114361174	RPTEC	kidney:	n/a
40	chr2:114359873-114359923	ovcar-3	ovarian:	n/a
41	chr2:114361124-114361174	AG04449	skin:	fetal
42	chr2:114359251-114359301	GM19239	blood:	n/a
43	chr2:114361124-114361174	HRE	kidney:	n/a
44	chr2:114359762-114359812	HEK293	kidney:	embryo
45	chr2:114359873-114359923	K562	blood:	n/a
46	chr2:114361124-114361174	ECC-1	luminal epithelium:	n/a
47	chr2:114359873-114359923	AG04449	skin:	fetal
48	chr2:114359762-114359812	HPAEpiC	pulmonary alveolar:	n/a
49	chr2:114361925-114361975	HepG2	liver:	n/a
50	chr2:114359188-114359238	ProgFib	skin:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:114359257..114359811-chr2:114457510..114458087,2	MCF-7	breast:
2	chr2:114361263..114362251-chr2:114457536..114458288,3	MCF-7	breast:
3	chr2:114344560..114345063-chr2:114361338..114362244,2	MCF-7	breast:
4	chr2:114361748..114362273-chr21:48118691..48119211,2	MCF-7	breast:
5	chr2:114361344..114362249-chr2:114457515..114458330,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC35F5-14	chr2:114379645-114379738	NONHSAT073823
2	lnc-SLC35F5-15	chr2:114364924-114365485	NONHSAT073814
3	lnc-SLC35F5-16	chr2:114358789-114359153	NONHSAT073811
4	lnc-SLC35F5-16	chr2:114358789-114359153	NONHSAT073810
5	lnc-SLC35F5-14	chr2:114379690-114379738	NONHSAT073821
6	lnc-SLC35F5-14	chr2:114379303-114379593	NONHSAT073820
7	lnc-SLC35F5-14	chr2:114379690-114379738	NONHSAT073822
8	lnc-SLC35F5-16	chr2:114361172-114361294	NONHSAT073809
9	lnc-SLC35F5-15	chr2:114363444-114364918	NONHSAT073814
10	lnc-SLC35F5-14	chr2:114379303-114379593	NONHSAT073821
11	lnc-SLC35F5-16	chr2:114358789-114359006	NONHSAT073809
12	lnc-SLC35F5-14	chr2:114379409-114379596	NONHSAT073822

No data

Variant related genes	Relation type
RABL2A	TF binding region
RPL23AP7	TF binding region
DDX11L2	TF binding region
RABL2A	CpG island
RPL23AP7	CpG island
DDX11L2	CpG island

Extended variants
information (count: 794 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62162365	chr2:114358942-114358943	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs371893258	chr2:114359000-114359001	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs553526099	chr2:114359010-114359011	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs573531221	chr2:114359040-114359041	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs536140383	chr2:114359042-114359043	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs555995626	chr2:114359060-114359061	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs146209431	chr2:114359070-114359071	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs57442816	chr2:114359095-114359096	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs544248522	chr2:114359170-114359171	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs564528259	chr2:114359208-114359209	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs7349310	chr2:114359213-114359214	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs373798661	chr2:114359227-114359228	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs185315296	chr2:114359233-114359234	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs11489987	chr2:114359234-114359235	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs368761412	chr2:114359282-114359283	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs112251957	chr2:114359289-114359290	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs7567469	chr2:114359292-114359293	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs7340323	chr2:114359323-114359324	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs7340221	chr2:114359338-114359339	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs7349236	chr2:114359341-114359342	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs540765267	chr2:114359343-114359344	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs560659824	chr2:114359370-114359371	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs2758122	chr2:114359409-114359410	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs529558084	chr2:114359416-114359417	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs200788173	chr2:114359435-114359436	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs368682297	chr2:114359446-114359447	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs7349239	chr2:114359484-114359485	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs7340224	chr2:114359486-114359487	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs6542164	chr2:114359507-114359508	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs7349380	chr2:114359537-114359538	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs3888754	chr2:114359545-114359546	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs532045565	chr2:114359582-114359583	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs7349240	chr2:114359620-114359621	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs62162370	chr2:114359624-114359625	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs11490624	chr2:114359626-114359627	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs551059516	chr2:114359698-114359699	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs571246520	chr2:114359717-114359718	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs9653425	chr2:114359737-114359738	Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs7340386	chr2:114359744-114359745	Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs113533093	chr2:114359754-114359755	Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs114229670	chr2:114359767-114359768	Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs147484486	chr2:114359775-114359776	Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs75788979	chr2:114359776-114359777	Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	mRNA abundance
44	rs567028498	chr2:114359780-114359781	Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs190118182	chr2:114359782-114359783	Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs374055143	chr2:114359786-114359787	Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs527963425	chr2:114359791-114359792	Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs182807066	chr2:114359804-114359805	Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs576230295	chr2:114359806-114359807	Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs144329639	chr2:114359813-114359814	Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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	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
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
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114342400-114360800	Weak transcription	Esophagus	oesophagus
2	chr2:114342600-114360600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:114342600-114360800	Weak transcription	Brain Germinal Matrix	brain
4	chr2:114342800-114360000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr2:114342800-114360000	Weak transcription	Placenta	Placenta
6	chr2:114342800-114360000	Weak transcription	Thymus	Thymus
7	chr2:114342800-114360600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:114342800-114360600	Weak transcription	Psoas Muscle	Psoas
9	chr2:114342800-114360800	Weak transcription	Aorta	Aorta
10	chr2:114342800-114360800	Weak transcription	Ovary	ovary
11	chr2:114343000-114360400	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr2:114343000-114360600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr2:114343000-114360600	Weak transcription	Stomach Smooth Muscle	stomach
14	chr2:114343000-114360600	Weak transcription	HSMMtube	muscle
15	chr2:114343000-114360800	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr2:114343000-114361000	Weak transcription	Small Intestine	intestine
17	chr2:114343200-114360400	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr2:114343200-114360600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr2:114343200-114360600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr2:114343200-114360600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr2:114343200-114360600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr2:114343200-114360600	Weak transcription	Duodenum Mucosa	Duodenum
23	chr2:114343200-114360600	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr2:114343200-114360600	Weak transcription	NHLF	lung
25	chr2:114343200-114360800	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr2:114343200-114360800	Weak transcription	Liver	Liver
27	chr2:114343400-114359800	Weak transcription	Dnd41	blood
28	chr2:114345600-114360200	Weak transcription	Fetal Heart	heart
29	chr2:114345600-114360600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr2:114345800-114360400	Weak transcription	Primary B cells from peripheral blood	blood
31	chr2:114346000-114360200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr2:114346000-114360600	Weak transcription	Right Ventricle	heart
33	chr2:114346000-114361000	Weak transcription	Stomach Mucosa	stomach
34	chr2:114347600-114360600	Weak transcription	Colonic Mucosa	Colon
35	chr2:114347800-114360600	Weak transcription	Pancreas	Pancrea
36	chr2:114350000-114360000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr2:114350000-114360000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr2:114350000-114360400	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr2:114350000-114360600	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr2:114350000-114360600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr2:114350000-114360600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr2:114350000-114360600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr2:114350000-114360600	Weak transcription	Brain Cingulate Gyrus	brain
44	chr2:114350000-114360600	Weak transcription	Brain Hippocampus Middle	brain
45	chr2:114350000-114360600	Weak transcription	Left Ventricle	heart
46	chr2:114350000-114360600	Weak transcription	Lung	lung
47	chr2:114350000-114360600	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr2:114350000-114360800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr2:114350200-114360400	Weak transcription	Primary T cells from cord blood	blood
50	chr2:114350200-114360400	Weak transcription	Primary T cells fromperipheralblood	blood

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