Variant report

Variant	nsv1047117
Chromosome Location	chr10:46027942-46075946
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:277)
CpG islands
(count:428)
Chromatin interactive
region (count:17)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:277 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:46053837-46054169	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:46053147-46053169	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:46073900-46074203	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:46071413-46072318	HepG2	liver:	n/a	n/a
5	BATF	chr10:46048680-46048912	GM12878	blood:	n/a	n/a
6	BATF	chr10:46048777-46048912	GM12878	blood:	n/a	n/a
7	BHLHE40	chr10:46049120-46049135	GM12878	blood:	n/a	n/a
8	BHLHE40	chr10:46075877-46076884	GM12878	blood:	n/a	n/a
9	BHLHE40	chr10:46071505-46071697	HepG2	liver:	n/a	n/a
10	CBX3	chr10:46070238-46070703	K562	blood:	n/a	n/a
11	CBX3	chr10:46052839-46053381	K562	blood:	n/a	n/a
12	CBX3	chr10:46052948-46053303	K562	blood:	n/a	n/a
13	CEBPB	chr10:46051289-46051641	IMR90	lung:	n/a	chr10:46051446-46051457 chr10:46051433-46051444
14	CEBPB	chr10:46040674-46040941	A549	lung:	n/a	chr10:46040811-46040822
15	CEBPB	chr10:46064920-46065043	HepG2	liver:	n/a	chr10:46064929-46064940
16	CEBPB	chr10:46051286-46051631	Hela-S3	cervix:	n/a	chr10:46051446-46051457 chr10:46051433-46051444
17	CEBPB	chr10:46072292-46072465	HepG2	liver:	n/a	chr10:46072355-46072366
18	CEBPB	chr10:46040656-46041003	K562	blood:	n/a	chr10:46040811-46040822
19	CEBPB	chr10:46074482-46074642	K562	blood:	n/a	n/a
20	CEBPB	chr10:46051298-46051581	A549	lung:	n/a	chr10:46051446-46051457 chr10:46051433-46051444
21	CEBPB	chr10:46051316-46051621	HepG2	liver:	n/a	chr10:46051446-46051457 chr10:46051433-46051444
22	CEBPB	chr10:46040650-46040978	HepG2	liver:	n/a	chr10:46040811-46040822
23	CEBPB	chr10:46051317-46051601	K562	blood:	n/a	chr10:46051446-46051457 chr10:46051433-46051444
24	CHD1	chr10:46075818-46076469	GM12878	blood:	n/a	n/a
25	CTCF	chr10:46061414-46061448	GM12878	blood:	n/a	n/a
26	CTCF	chr10:46040720-46040870	HEK293	kidney:	n/a	n/a
27	CTCF	chr10:46040740-46040890	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr10:46040640-46040790	GM12873	blood:	n/a	n/a
29	CTCF	chr10:46053980-46054130	HepG2	liver:	n/a	n/a
30	CTCF	chr10:46040780-46040930	HEK293	kidney:	n/a	n/a
31	CTCF	chr10:46061374-46061559	GM12878	blood:	n/a	n/a
32	CTCF	chr10:46037549-46037576	GM10266	blood:	n/a	n/a
33	CTCF	chr10:46053940-46054090	HepG2	liver:	n/a	n/a
34	CUX1	chr10:46074023-46074510	K562	blood:	n/a	n/a
35	CUX1	chr10:46075810-46077334	K562	blood:	n/a	n/a
36	CUX1	chr10:46075876-46076829	GM12878	blood:	n/a	n/a
37	EGR1	chr10:46070609-46070818	K562	blood:	n/a	n/a
38	ELF1	chr10:46052974-46053372	K562	blood:	n/a	chr10:46053152-46053163 chr10:46053133-46053144 chr10:46053131-46053144 chr10:46053151-46053164
39	ELF1	chr10:46052944-46053351	HepG2	liver:	n/a	chr10:46053152-46053163 chr10:46053133-46053144 chr10:46053131-46053144 chr10:46053151-46053164
40	ELF1	chr10:46052953-46053310	HepG2	liver:	n/a	chr10:46053152-46053163 chr10:46053133-46053144 chr10:46053131-46053144 chr10:46053151-46053164
41	EP300	chr10:46048685-46048885	GM12878	blood:	n/a	n/a
42	EP300	chr10:46075827-46076259	GM12878	blood:	n/a	chr10:46075915-46075928 chr10:46076105-46076119
43	EP300	chr10:46052028-46052102	K562	blood:	n/a	chr10:46052077-46052086
44	EP300	chr10:46061655-46062492	SK-N-SH	brain:	n/a	n/a
45	EP300	chr10:46071337-46071888	HepG2	liver:	n/a	n/a
46	EP300	chr10:46073841-46074302	HepG2	liver:	n/a	n/a
47	EP300	chr10:46055663-46055986	HepG2	liver:	n/a	n/a
48	EP300	chr10:46052962-46053305	K562	blood:	n/a	n/a
49	EP300	chr10:46055751-46055946	K562	blood:	n/a	n/a
50	EP300	chr10:46053849-46053902	K562	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:46029359-46029409	AG04450	lung:	fetal
2	chr10:46029359-46029409	AG04450	lung:	fetal
3	chr10:46029359-46029409	AG04449	skin:	fetal
4	chr10:46032181-46032231	AG04449	skin:	fetal
5	chr10:46032181-46032231	HEK293	kidney:	embryo
6	chr10:46032181-46032231	AG04450	lung:	fetal
7	chr10:46032181-46032231	ECC-1	luminal epithelium:	n/a
8	chr10:46032264-46032314	AoSMC	blood vessel:	n/a
9	chr10:46032264-46032314	GM12878	blood:	n/a
10	chr10:46030793-46030843	NT2-D1	testis:	n/a
11	chr10:46065860-46065910	RPTEC	kidney:	n/a
12	chr10:46053734-46053784	T-47D	breast:	n/a
13	chr10:46030793-46030843	HAEpiC	amniotic membrane:	n/a
14	chr10:46029359-46029409	AoSMC	blood vessel:	n/a
15	chr10:46053734-46053784	HCT-116	colon:	n/a
16	chr10:46032202-46032252	NB4	blood:	n/a
17	chr10:46032202-46032252	HCT-116	colon:	n/a
18	chr10:46029359-46029409	NT2-D1	testis:	n/a
19	chr10:46032264-46032314	HNPCEpiC	eye:	n/a
20	chr10:46065860-46065910	HUVEC	blood vessel:	n/a
21	chr10:46032181-46032231	ProgFib	skin:	n/a
22	chr10:46032264-46032314	HAEpiC	amniotic membrane:	n/a
23	chr10:46032202-46032252	GM12892	blood:	n/a
24	chr10:46065860-46065910	HCF	heart:	n/a
25	chr10:46030793-46030843	NHDF-neo	bronchial:	n/a
26	chr10:46030793-46030843	SK-N-SH_RA	brain:	n/a
27	chr10:46032264-46032314	SAEC	small airway:	n/a
28	chr10:46053734-46053784	HUVEC	blood vessel:	n/a
29	chr10:46032202-46032252	AG10803	skin:	n/a
30	chr10:46032264-46032314	MCF10A-Er-Src	breast:	n/a
31	chr10:46030793-46030843	BJ	skin:	n/a
32	chr10:46053734-46053784	GM06990	blood:	n/a
33	chr10:46032202-46032252	PANC-1	pancreas:	n/a
34	chr10:46029359-46029409	U87	brain:	n/a
35	chr10:46032264-46032314	HEK293	kidney:	embryo
36	chr10:46032181-46032231	ovcar-3	ovarian:	n/a
37	chr10:46065860-46065910	NHDF-neo	bronchial:	n/a
38	chr10:46032202-46032252	HPAEpiC	pulmonary alveolar:	n/a
39	chr10:46053734-46053784	GM12892	blood:	n/a
40	chr10:46030793-46030843	AG04450	lung:	fetal
41	chr10:46032181-46032231	AG09319	gingival:	n/a
42	chr10:46053734-46053784	HepG2	liver:	n/a
43	chr10:46065860-46065910	HCM	heart:	n/a
44	chr10:46029359-46029409	HIPEpiC	eye:	n/a
45	chr10:46032202-46032252	NH-A	brain:	n/a
46	chr10:46032181-46032231	HUVEC	blood vessel:	n/a
47	chr10:46029359-46029409	NHBE	bronchial:	n/a
48	chr10:46032202-46032252	NHBE	bronchial:	n/a
49	chr10:46030793-46030843	GM06990	blood:	n/a
50	chr10:46030793-46030843	HRPEpiC	eye:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:46047681..46050727-chr10:46051442..46055483,4	K562	blood:
2	chr10:46042311..46044795-chr10:46052336..46053839,2	K562	blood:
3	chr10:46043857..46045748-chr10:46047438..46049398,2	K562	blood:
4	chr10:46054558..46056066-chr10:46056809..46059379,2	K562	blood:
5	chr10:46047681..46050727-chr10:46051442..46055483,4	K562	blood:
6	chr10:46074816..46082903-chr10:46083299..46090228,15	K562	blood:
7	chr10:46049227..46053354-chr10:46053983..46058180,6	K562	blood:
8	chr10:46038014..46040186-chr10:46047906..46049912,2	K562	blood:
9	chr10:46042311..46044795-chr10:46052336..46053839,2	K562	blood:
10	chr10:46045209..46047210-chr10:46049150..46053014,3	K562	blood:
11	chr10:46038014..46040186-chr10:46047906..46049912,2	K562	blood:
12	chr10:46054558..46056066-chr10:46056809..46059379,2	K562	blood:
13	chr10:46045209..46047210-chr10:46049150..46053014,3	K562	blood:
14	chr10:46043857..46045748-chr10:46047438..46049398,2	K562	blood:
15	chr10:46049227..46053354-chr10:46053983..46058180,6	K562	blood:
16	chr10:46070111..46072532-chr10:46080912..46083330,2	K562	blood:
17	chr10:46075326..46077121-chr10:46078521..46080983,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 1826 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1826 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142280812	chr10:46027945-46027946	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573536044	chr10:46027956-46027957	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374740111	chr10:46027957-46027958	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1994426	chr10:46028010-46028011	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs189804749	chr10:46028018-46028019	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs144363881	chr10:46028144-46028145	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs550334447	chr10:46028194-46028195	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs376819028	chr10:46028255-46028256	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs562576446	chr10:46028340-46028341	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs182679373	chr10:46028347-46028348	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs548327042	chr10:46028388-46028389	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs538819401	chr10:46028434-46028435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188118859	chr10:46028452-46028453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147834018	chr10:46028465-46028466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552045759	chr10:46028512-46028513	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562055549	chr10:46028536-46028537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368170309	chr10:46028546-46028547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs77833583	chr10:46028557-46028558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140989641	chr10:46028599-46028600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201435975	chr10:46028610-46028611	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142329756	chr10:46028636-46028637	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538999551	chr10:46028638-46028639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557096388	chr10:46028652-46028653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371554606	chr10:46028665-46028666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111936295	chr10:46028683-46028684	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs58437785	chr10:46028698-46028699	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs536355299	chr10:46028732-46028733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112728054	chr10:46028761-46028762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555152880	chr10:46028776-46028777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192870852	chr10:46028789-46028790	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540869381	chr10:46028799-46028800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113286525	chr10:46028827-46028828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113349471	chr10:46028843-46028844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565556415	chr10:46028880-46028881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577489289	chr10:46028901-46028902	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544162711	chr10:46028932-46028933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150227081	chr10:46028950-46028951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76112318	chr10:46028959-46028960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547881237	chr10:46028977-46028978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559859583	chr10:46028996-46028997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115158558	chr10:46029000-46029001	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145085744	chr10:46029057-46029058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185330553	chr10:46029058-46029059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377584446	chr10:46029066-46029067	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374155074	chr10:46029079-46029080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570384165	chr10:46029081-46029082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537764958	chr10:46029088-46029089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550909732	chr10:46029161-46029162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569160808	chr10:46029217-46029218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536697459	chr10:46029218-46029219	Weak 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:781 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:46005400-46029800	Weak transcription	Fetal Kidney	kidney
2	chr10:46009400-46044400	Weak transcription	Thymus	Thymus
3	chr10:46010000-46056000	Weak transcription	Esophagus	oesophagus
4	chr10:46010200-46028800	Weak transcription	Rectal Smooth Muscle	rectum
5	chr10:46011600-46030200	Weak transcription	HepG2	liver
6	chr10:46014400-46070000	Weak transcription	Psoas Muscle	Psoas
7	chr10:46015600-46043400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr10:46017800-46029600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr10:46018000-46052800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr10:46018400-46040400	Weak transcription	K562	blood
11	chr10:46019200-46039200	Weak transcription	Fetal Intestine Large	intestine
12	chr10:46021200-46028000	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr10:46021400-46028000	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr10:46021800-46029400	Weak transcription	Brain Germinal Matrix	brain
15	chr10:46021800-46030200	Weak transcription	Primary B cells from cord blood	blood
16	chr10:46022000-46028800	Weak transcription	Placenta	Placenta
17	chr10:46022000-46029800	Weak transcription	Primary T cells from cord blood	blood
18	chr10:46022000-46030200	Weak transcription	Gastric	stomach
19	chr10:46022000-46030400	Weak transcription	Brain Cingulate Gyrus	brain
20	chr10:46022000-46032600	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr10:46022000-46043400	Weak transcription	Brain Angular Gyrus	brain
22	chr10:46022000-46046600	Weak transcription	Fetal Muscle Trunk	muscle
23	chr10:46022200-46028000	Weak transcription	Fetal Muscle Leg	muscle
24	chr10:46022200-46029800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr10:46022200-46030000	Weak transcription	Brain Substantia Nigra	brain
26	chr10:46022200-46043600	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr10:46022800-46030200	Weak transcription	Colon Smooth Muscle	Colon
28	chr10:46024400-46052800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr10:46024600-46044600	Weak transcription	Duodenum Mucosa	Duodenum
30	chr10:46025400-46028200	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr10:46025600-46029200	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr10:46025800-46028800	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr10:46026200-46057600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr10:46026400-46044400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr10:46026800-46028400	Strong transcription	Primary B cells from peripheral blood	blood
36	chr10:46027000-46028200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr10:46027000-46028400	Strong transcription	Adipose Nuclei	Adipose
38	chr10:46027000-46028400	Strong transcription	Brain Anterior Caudate	brain
39	chr10:46027000-46028800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr10:46027000-46028800	Strong transcription	Primary hematopoietic stem cells	blood
41	chr10:46027000-46028800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr10:46027000-46029600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr10:46027200-46028000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr10:46027200-46028000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr10:46027200-46028800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr10:46027200-46028800	Strong transcription	Rectal Mucosa Donor 29	rectum
47	chr10:46027200-46028800	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr10:46027200-46043200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
49	chr10:46027200-46047000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr10:46027400-46028000	Genic enhancers	Sigmoid Colon	Sigmoid Colon

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