Variant report

Variant	nsv1052233
Chromosome Location	chr10:46024620-46088061
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:359)
CpG islands
(count:488)
Chromatin interactive
region (count:23)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:359 , 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	chr10:46076689-46077359	K562	blood:	n/a	chr10:46076954-46076970
2	ARID3A	chr10:46053147-46053169	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:46053837-46054169	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:46071413-46072318	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:46073900-46074203	HepG2	liver:	n/a	n/a
6	BACH1	chr10:46083140-46083213	K562	blood:	n/a	n/a
7	BATF	chr10:46048680-46048912	GM12878	blood:	n/a	n/a
8	BATF	chr10:46048777-46048912	GM12878	blood:	n/a	n/a
9	BHLHE40	chr10:46075877-46076884	GM12878	blood:	n/a	n/a
10	BHLHE40	chr10:46049120-46049135	GM12878	blood:	n/a	n/a
11	BHLHE40	chr10:46071505-46071697	HepG2	liver:	n/a	n/a
12	CBX3	chr10:46085333-46085677	K562	blood:	n/a	n/a
13	CBX3	chr10:46070238-46070703	K562	blood:	n/a	n/a
14	CBX3	chr10:46052839-46053381	K562	blood:	n/a	n/a
15	CBX3	chr10:46052948-46053303	K562	blood:	n/a	n/a
16	CEBPB	chr10:46084467-46084734	HepG2	liver:	n/a	n/a
17	CEBPB	chr10:46051289-46051641	IMR90	lung:	n/a	chr10:46051446-46051457 chr10:46051433-46051444
18	CEBPB	chr10:46077515-46077744	HepG2	liver:	n/a	n/a
19	CEBPB	chr10:46040650-46040978	HepG2	liver:	n/a	chr10:46040811-46040822
20	CEBPB	chr10:46051286-46051631	Hela-S3	cervix:	n/a	chr10:46051446-46051457 chr10:46051433-46051444
21	CEBPB	chr10:46083592-46083777	K562	blood:	n/a	n/a
22	CEBPB	chr10:46040674-46040941	A549	lung:	n/a	chr10:46040811-46040822
23	CEBPB	chr10:46051317-46051601	K562	blood:	n/a	chr10:46051446-46051457 chr10:46051433-46051444
24	CEBPB	chr10:46051316-46051621	HepG2	liver:	n/a	chr10:46051446-46051457 chr10:46051433-46051444
25	CEBPB	chr10:46083584-46083771	HepG2	liver:	n/a	n/a
26	CEBPB	chr10:46051298-46051581	A549	lung:	n/a	chr10:46051446-46051457 chr10:46051433-46051444
27	CEBPB	chr10:46040656-46041003	K562	blood:	n/a	chr10:46040811-46040822
28	CEBPB	chr10:46084512-46084673	A549	lung:	n/a	n/a
29	CEBPB	chr10:46072292-46072465	HepG2	liver:	n/a	chr10:46072355-46072366
30	CEBPB	chr10:46064920-46065043	HepG2	liver:	n/a	chr10:46064929-46064940
31	CEBPB	chr10:46074482-46074642	K562	blood:	n/a	n/a
32	CHD1	chr10:46075818-46076469	GM12878	blood:	n/a	n/a
33	CHD2	chr10:46076349-46076680	GM12878	blood:	n/a	n/a
34	CTCF	chr10:46037549-46037576	GM10266	blood:	n/a	n/a
35	CTCF	chr10:46061374-46061559	GM12878	blood:	n/a	n/a
36	CTCF	chr10:46053980-46054130	HepG2	liver:	n/a	n/a
37	CTCF	chr10:46053940-46054090	HepG2	liver:	n/a	n/a
38	CTCF	chr10:46040780-46040930	HEK293	kidney:	n/a	n/a
39	CTCF	chr10:46040640-46040790	GM12873	blood:	n/a	n/a
40	CTCF	chr10:46076720-46076870	GM12873	blood:	n/a	n/a
41	CTCF	chr10:46061414-46061448	GM12878	blood:	n/a	n/a
42	CTCF	chr10:46040720-46040870	HEK293	kidney:	n/a	n/a
43	CTCF	chr10:46040740-46040890	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr10:46076620-46076770	K562	blood:	n/a	n/a
45	CTCF	chr10:46080540-46080690	HCM	heart:	n/a	n/a
46	CUX1	chr10:46077216-46077435	GM12878	blood:	n/a	n/a
47	CUX1	chr10:46075810-46077334	K562	blood:	n/a	n/a
48	CUX1	chr10:46075876-46076829	GM12878	blood:	n/a	n/a
49	CUX1	chr10:46074023-46074510	K562	blood:	n/a	n/a
50	EBF1	chr10:46076354-46076794	GM12878	blood:	n/a	chr10:46076585-46076596

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:46032264-46032314	HUVEC	blood vessel:	n/a
2	chr10:46065860-46065910	HepG2	liver:	n/a
3	chr10:46076550-46076600	K562	blood:	n/a
4	chr10:46076550-46076600	ovcar-3	ovarian:	n/a
5	chr10:46029359-46029409	GM12892	blood:	n/a
6	chr10:46029359-46029409	Hepatocyte	liver:	n/a
7	chr10:46065860-46065910	NB4	blood:	n/a
8	chr10:46053734-46053784	RPTEC	kidney:	n/a
9	chr10:46065860-46065910	SAEC	small airway:	n/a
10	chr10:46032264-46032314	HMEC	breast:	n/a
11	chr10:46053734-46053784	Hepatocyte	liver:	n/a
12	chr10:46053734-46053784	AG10803	skin:	n/a
13	chr10:46032264-46032314	NB4	blood:	n/a
14	chr10:46029359-46029409	H1-hESC	embryonic stem cell:	embryo
15	chr10:46032202-46032252	SK-N-SH_RA	brain:	n/a
16	chr10:46029359-46029409	Hela-S3	cervix:	n/a
17	chr10:46065860-46065910	AG04450	lung:	fetal
18	chr10:46030793-46030843	AG09309	skin:	n/a
19	chr10:46032202-46032252	GM06990	blood:	n/a
20	chr10:46032202-46032252	SK-N-MC	brain:	n/a
21	chr10:46065860-46065910	Hepatocyte	liver:	n/a
22	chr10:46032264-46032314	NHDF-neo	bronchial:	n/a
23	chr10:46065860-46065910	HCM	heart:	n/a
24	chr10:46032181-46032231	AG09309	skin:	n/a
25	chr10:46065860-46065910	SK-N-SH_RA	brain:	n/a
26	chr10:46030793-46030843	HRPEpiC	eye:	n/a
27	chr10:46032264-46032314	CMK	blood:	n/a
28	chr10:46032202-46032252	HEK293	kidney:	embryo
29	chr10:46032202-46032252	HPAEpiC	pulmonary alveolar:	n/a
30	chr10:46053734-46053784	NHBE	bronchial:	n/a
31	chr10:46076550-46076600	GM12878	blood:	n/a
32	chr10:46053734-46053784	IMR90	lung:	fetal
33	chr10:46029359-46029409	HPAEpiC	pulmonary alveolar:	n/a
34	chr10:46065860-46065910	HPAEpiC	pulmonary alveolar:	n/a
35	chr10:46030793-46030843	SKMC	muscle:	n/a
36	chr10:46065860-46065910	BJ	skin:	n/a
37	chr10:46032202-46032252	PANC-1	pancreas:	n/a
38	chr10:46076550-46076600	HUVEC	blood vessel:	n/a
39	chr10:46065860-46065910	HRCEpiC	kidney:	n/a
40	chr10:46032181-46032231	HL-60	blood:	n/a
41	chr10:46032181-46032231	HCPEpiC	choroid plexus:	n/a
42	chr10:46030793-46030843	A549	lung:	n/a
43	chr10:46032181-46032231	RPTEC	kidney:	n/a
44	chr10:46053734-46053784	Hela-S3	cervix:	n/a
45	chr10:46029359-46029409	GM19239	blood:	n/a
46	chr10:46029359-46029409	NH-A	brain:	n/a
47	chr10:46065860-46065910	K562	blood:	n/a
48	chr10:46029359-46029409	NB4	blood:	n/a
49	chr10:46053734-46053784	T-47D	breast:	n/a
50	chr10:46032181-46032231	GM12891	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:46038014..46040186-chr10:46047906..46049912,2	K562	blood:
2	chr10:46014012..46015571-chr10:46081118..46083546,2	K562	blood:
3	chr10:46038014..46040186-chr10:46047906..46049912,2	K562	blood:
4	chr10:46074816..46082903-chr10:46083299..46090228,15	K562	blood:
5	chr10:46049227..46053354-chr10:46053983..46058180,6	K562	blood:
6	chr10:46043857..46045748-chr10:46047438..46049398,2	K562	blood:
7	chr10:46042311..46044795-chr10:46052336..46053839,2	K562	blood:
8	chr10:46075326..46077121-chr10:46078521..46080983,2	K562	blood:
9	chr10:46054558..46056066-chr10:46056809..46059379,2	K562	blood:
10	chr10:46083877..46085539-chr10:46088603..46090274,2	K562	blood:
11	chr10:46047681..46050727-chr10:46051442..46055483,4	K562	blood:
12	chr10:46045209..46047210-chr10:46049150..46053014,3	K562	blood:
13	chr10:46079502..46081170-chr10:46092167..46094339,3	K562	blood:
14	chr10:46042311..46044795-chr10:46052336..46053839,2	K562	blood:
15	chr10:46017813..46021385-chr10:46021525..46026200,4	K562	blood:
16	chr10:46047681..46050727-chr10:46051442..46055483,4	K562	blood:
17	chr10:46045209..46047210-chr10:46049150..46053014,3	K562	blood:
18	chr10:46070111..46072532-chr10:46080912..46083330,2	K562	blood:
19	chr10:46043857..46045748-chr10:46047438..46049398,2	K562	blood:
20	chr10:46054558..46056066-chr10:46056809..46059379,2	K562	blood:
21	chr10:46075326..46077121-chr10:46078521..46080983,2	K562	blood:
22	chr10:46070111..46072532-chr10:46080912..46083330,2	K562	blood:
23	chr10:46049227..46053354-chr10:46053983..46058180,6	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALOX5-1	chr10:46045257-46045361	NONHSAT013106
2	lnc-ALOX5-1	chr10:46043743-46043887	NONHSAT013106
3	lnc-ALOX5-1	chr10:46056139-46056282	NONHSAT013106
4	lnc-ZFAND4-1	chr10:46048560-46048652	NONHSAT013107

No data

Variant related genes	Relation type
MARCH8	TF binding region
MARCH8	CpG island
ENSG00000165406	chromatin interactions

Extended variants
information (count: 2330 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2330 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1073525	chr10:46024620-46024621	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566003870	chr10:46024656-46024657	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1072740	chr10:46024674-46024675	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34897497	chr10:46024677-46024678	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs73287387	chr10:46024693-46024694	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs11239550	chr10:46024729-46024730	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
7	rs555154169	chr10:46024741-46024742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182364856	chr10:46024742-46024743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186630502	chr10:46024774-46024775	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568579599	chr10:46024802-46024803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191131333	chr10:46024808-46024809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545323302	chr10:46024838-46024839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563619596	chr10:46024855-46024856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184789446	chr10:46024870-46024871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550180875	chr10:46024953-46024954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12775527	chr10:46024990-46024991	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs147611287	chr10:46024994-46024995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547551542	chr10:46025134-46025135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142137132	chr10:46025175-46025176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146006764	chr10:46025221-46025222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs117126848	chr10:46025234-46025235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551649717	chr10:46025237-46025238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545490957	chr10:46025314-46025315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138351094	chr10:46025332-46025333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555365060	chr10:46025344-46025345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556333350	chr10:46025369-46025370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573622743	chr10:46025381-46025382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534726947	chr10:46025393-46025394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142440667	chr10:46025412-46025413	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs189737976	chr10:46025413-46025414	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs545261727	chr10:46025422-46025423	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs563556825	chr10:46025498-46025499	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs546313950	chr10:46025545-46025546	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs192935193	chr10:46025580-46025581	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs576111862	chr10:46025581-46025582	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs12269403	chr10:46025611-46025612	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs564537229	chr10:46025678-46025679	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs72798212	chr10:46025712-46025713	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs529328447	chr10:46025762-46025763	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs143231569	chr10:46025775-46025776	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs148310646	chr10:46025808-46025809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540608955	chr10:46025845-46025846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533335272	chr10:46025872-46025873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551588596	chr10:46025908-46025909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185223313	chr10:46025927-46025928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs72798213	chr10:46025932-46025933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189636547	chr10:46025946-46025947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79255254	chr10:46025998-46025999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537499276	chr10:46026008-46026009	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530709395	chr10:46026032-46026033	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioblastoma multiforme	21138945	CNVD
Autism	19287141	CNVD
Intellectual disability	21948486	CNVD
Glioblastoma multiforme	21525872	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1259 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45999000-46025600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr10:46005000-46025200	Weak transcription	Primary B cells from peripheral blood	blood
3	chr10:46005400-46029800	Weak transcription	Fetal Kidney	kidney
4	chr10:46007800-46027400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr10:46008400-46027200	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr10:46009400-46044400	Weak transcription	Thymus	Thymus
7	chr10:46010000-46027800	Weak transcription	Lung	lung
8	chr10:46010000-46056000	Weak transcription	Esophagus	oesophagus
9	chr10:46010200-46027200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr10:46010200-46028800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr10:46010800-46025600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr10:46011000-46025400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr10:46011400-46027200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr10:46011600-46030200	Weak transcription	HepG2	liver
15	chr10:46013200-46027400	Weak transcription	Left Ventricle	heart
16	chr10:46014000-46027400	Weak transcription	Fetal Intestine Small	intestine
17	chr10:46014400-46070000	Weak transcription	Psoas Muscle	Psoas
18	chr10:46015000-46025600	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr10:46015400-46025800	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr10:46015600-46026000	Weak transcription	Aorta	Aorta
21	chr10:46015600-46043400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr10:46016000-46027400	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr10:46016200-46027400	Weak transcription	Liver	Liver
24	chr10:46017200-46027000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr10:46017800-46027200	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr10:46017800-46029600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr10:46018000-46052800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr10:46018400-46027200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr10:46018400-46040400	Weak transcription	K562	blood
30	chr10:46018800-46027600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr10:46019200-46039200	Weak transcription	Fetal Intestine Large	intestine
32	chr10:46021200-46028000	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr10:46021400-46028000	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr10:46021800-46029400	Weak transcription	Brain Germinal Matrix	brain
35	chr10:46021800-46030200	Weak transcription	Primary B cells from cord blood	blood
36	chr10:46022000-46027000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr10:46022000-46027400	Weak transcription	Fetal Lung	lung
38	chr10:46022000-46027400	Weak transcription	Fetal Stomach	stomach
39	chr10:46022000-46027400	Weak transcription	Ovary	ovary
40	chr10:46022000-46027400	Weak transcription	Pancreas	Pancrea
41	chr10:46022000-46027400	Weak transcription	Stomach Smooth Muscle	stomach
42	chr10:46022000-46027600	Weak transcription	Brain Hippocampus Middle	brain
43	chr10:46022000-46027800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr10:46022000-46028800	Weak transcription	Placenta	Placenta
45	chr10:46022000-46029800	Weak transcription	Primary T cells from cord blood	blood
46	chr10:46022000-46030200	Weak transcription	Gastric	stomach
47	chr10:46022000-46030400	Weak transcription	Brain Cingulate Gyrus	brain
48	chr10:46022000-46032600	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr10:46022000-46043400	Weak transcription	Brain Angular Gyrus	brain
50	chr10:46022000-46046600	Weak transcription	Fetal Muscle Trunk	muscle

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