Variant report

Variant	nsv1014479
Chromosome Location	chr2:213370690-213413231
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:599)
CpG islands
(count:1221)
Chromatin interactive
region (count:15)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:599 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:213400803-213401775	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:213401997-213402263	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:213402946-213403789	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr2:213370363-213370703	GM12878	blood:	n/a	chr2:213370531-213370542
5	BRCA1	chr2:213402263-213402279	HepG2	liver:	n/a	n/a
6	CEBPB	chr2:213375009-213375063	H1-hESC	embryonic stem cell:	n/a	chr2:213375009-213375018 chr2:213375009-213375020 chr2:213375009-213375018 chr2:213375009-213375018 chr2:213375009-213375018
7	CEBPB	chr2:213374877-213375196	HepG2	liver:	n/a	chr2:213375009-213375018 chr2:213375009-213375020 chr2:213375009-213375018 chr2:213375007-213375018 chr2:213375009-213375018 chr2:213375009-213375018 chr2:213375007-213375020
8	CEBPB	chr2:213401039-213401263	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr2:213402488-213402825	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr2:213413184-213413476	HepG2	liver:	n/a	chr2:213413325-213413336
11	CEBPB	chr2:213374901-213375173	IMR90	lung:	n/a	chr2:213375009-213375018 chr2:213375009-213375020 chr2:213375009-213375018 chr2:213375007-213375018 chr2:213375009-213375018 chr2:213375009-213375018 chr2:213375007-213375020
12	CEBPB	chr2:213403563-213404207	Hela-S3	cervix:	n/a	n/a
13	CHD1	chr2:213402626-213402790	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr2:213403476-213404207	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr2:213402257-213402830	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr2:213402431-213402438	HepG2	liver:	n/a	n/a
17	CHD2	chr2:213403694-213404221	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTBP2	chr2:213400916-213404322	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr2:213401360-213401510	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr2:213385200-213385350	GM12870	blood:	n/a	n/a
21	CTCF	chr2:213393200-213393350	GM12864	blood:	n/a	n/a
22	CTCF	chr2:213402580-213402730	BE2_C	brain:	n/a	chr2:213402588-213402601
23	CTCF	chr2:213401360-213401510	HRE	kidney:	n/a	n/a
24	CTCF	chr2:213397420-213397570	BE2_C	brain:	n/a	n/a
25	CTCF	chr2:213402638-213402725	Fibrobl	skin:	n/a	n/a
26	CTCF	chr2:213382583-213382660	LNCaP	prostate:	n/a	chr2:213382593-213382611 chr2:213382595-213382608
27	CTCF	chr2:213385075-213385347	HepG2	liver:	n/a	n/a
28	CTCF	chr2:213413220-213413370	GM12878	blood:	n/a	chr2:213413330-213413351
29	CTCF	chr2:213385172-213385341	NHEK	skin:	n/a	n/a
30	CTCF	chr2:213385140-213385290	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr2:213382540-213382690	HRPEpiC	eye:	n/a	chr2:213382593-213382611 chr2:213382595-213382608
32	CTCF	chr2:213401920-213402070	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr2:213385260-213385410	HCT-116	colon:	n/a	n/a
34	CTCF	chr2:213401420-213401570	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr2:213382560-213382710	AG10803	skin:	n/a	chr2:213382593-213382611 chr2:213382595-213382608
36	CTCF	chr2:213412900-213413050	HPF	lung:	n/a	n/a
37	CTCF	chr2:213393220-213393370	RPTEC	kidney:	n/a	n/a
38	CTCF	chr2:213385180-213385330	HMEC	breast:	n/a	n/a
39	CTCF	chr2:213402617-213402734	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:213385200-213385350	BJ	skin:	n/a	n/a
41	CTCF	chr2:213393280-213393430	AG09319	gingival:	n/a	n/a
42	CTCF	chr2:213385160-213385310	BE2_C	brain:	n/a	n/a
43	CTCF	chr2:213393320-213393470	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr2:213397280-213397430	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr2:213382486-213382759	GM12878	blood:	n/a	chr2:213382593-213382611 chr2:213382595-213382608
46	CTCF	chr2:213397380-213397530	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr2:213385220-213385370	AG04450	lung:	n/a	n/a
48	CTCF	chr2:213385180-213385330	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr2:213393156-213393607	HCT-116	colon:	n/a	n/a
50	CTCF	chr2:213402540-213402690	AG09319	gingival:	n/a	chr2:213402588-213402601

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:213401565-213401615	HPAEpiC	pulmonary alveolar:	n/a
2	chr2:213401565-213401615	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:213401333-213401383	RPTEC	kidney:	n/a
4	chr2:213403960-213404010	HMEC	breast:	n/a
5	chr2:213400869-213400919	PANC-1	pancreas:	n/a
6	chr2:213403960-213404010	NB4	blood:	n/a
7	chr2:213403734-213403784	H1-hESC	embryonic stem cell:	embryo
8	chr2:213401195-213401245	NT2-D1	testis:	n/a
9	chr2:213401996-213402046	CMK	blood:	n/a
10	chr2:213403960-213404010	ECC-1	luminal epithelium:	n/a
11	chr2:213403929-213403979	Caco-2	colon:	n/a
12	chr2:213401333-213401383	PFSK-1	brain:	n/a
13	chr2:213406960-213407010	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:213403929-213403979	MCF-7	breast:	n/a
15	chr2:213403929-213403979	HRPEpiC	eye:	n/a
16	chr2:213401195-213401245	SK-N-SH_RA	brain:	n/a
17	chr2:213401056-213401106	HCPEpiC	choroid plexus:	n/a
18	chr2:213401333-213401383	HPAEpiC	pulmonary alveolar:	n/a
19	chr2:213401996-213402046	HRCEpiC	kidney:	n/a
20	chr2:213400869-213400919	Hepatocyte	liver:	n/a
21	chr2:213401544-213401594	MCF10A-Er-Src	breast:	n/a
22	chr2:213403321-213403371	SKMC	muscle:	n/a
23	chr2:213400697-213400747	U87	brain:	n/a
24	chr2:213403859-213403909	HEK293	kidney:	embryo
25	chr2:213401565-213401615	PANC-1	pancreas:	n/a
26	chr2:213401565-213401615	AoSMC	blood vessel:	n/a
27	chr2:213401544-213401594	HRE	kidney:	n/a
28	chr2:213403321-213403371	HIPEpiC	eye:	n/a
29	chr2:213402433-213402483	HRPEpiC	eye:	n/a
30	chr2:213403321-213403371	HRPEpiC	eye:	n/a
31	chr2:213403859-213403909	NT2-D1	testis:	n/a
32	chr2:213401056-213401106	NHBE	bronchial:	n/a
33	chr2:213403212-213403262	NHDF-neo	bronchial:	n/a
34	chr2:213403212-213403262	HNPCEpiC	eye:	n/a
35	chr2:213401565-213401615	A549	lung:	n/a
36	chr2:213403960-213404010	NT2-D1	testis:	n/a
37	chr2:213402181-213402231	GM12891	blood:	n/a
38	chr2:213402815-213402865	RPTEC	kidney:	n/a
39	chr2:213403212-213403262	U87	brain:	n/a
40	chr2:213401544-213401594	IMR90	lung:	fetal
41	chr2:213401996-213402046	HEEpiC	esophagus:	n/a
42	chr2:213401565-213401615	Jurkat	blood:	n/a
43	chr2:213403960-213404010	BE2_C	brain:	n/a
44	chr2:213402433-213402483	ovcar-3	ovarian:	n/a
45	chr2:213401544-213401594	NH-A	brain:	n/a
46	chr2:213402433-213402483	MCF-7	breast:	n/a
47	chr2:213402181-213402231	AG09309	skin:	n/a
48	chr2:213402181-213402231	IMR90	lung:	fetal
49	chr2:213402815-213402865	HEEpiC	esophagus:	n/a
50	chr2:213403212-213403262	HEK293	kidney:	embryo

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:213401536..213403038-chr2:213405253..213408127,2	MCF-7	breast:
2	chr2:211949622..211950636-chr2:213412760..213413513,3	MCF-7	breast:
3	chr2:213392043..213394903-chr2:213396609..213399566,4	MCF-7	breast:
4	chr17:57924251..57926616-chr2:213401786..213403830,2	MCF-7	breast:
5	chr2:213392043..213394903-chr2:213396609..213399566,4	MCF-7	breast:
6	chr2:213401917..213403622-chr2:213408443..213409958,2	MCF-7	breast:
7	chr2:213392919..213394585-chr2:213396394..213398532,2	K562	blood:
8	chr2:212742372..212744206-chr2:213400637..213402216,2	MCF-7	breast:
9	chr2:213394025..213397226-chr2:213401428..213405238,3	MCF-7	breast:
10	chr2:212099679..212101187-chr2:213398262..213400932,2	MCF-7	breast:
11	chr2:213401536..213403038-chr2:213405253..213408127,2	MCF-7	breast:
12	chr2:213392919..213394585-chr2:213396394..213398532,2	K562	blood:
13	chr2:213370671..213373168-chr2:213375734..213377389,2	MCF-7	breast:
14	chr2:213042144..213043012-chr2:213382544..213383068,2	MCF-7	breast:
15	chr2:213370671..213373168-chr2:213375734..213377389,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAG16-10	chr2:213389892-213390223	l_2023_chr2:213368288-213390223_testes
2	lnc-SPAG16-10	chr2:213384075-213384142	l_2023_chr2:213368288-213390223_testes

No data

Variant related genes	Relation type
ERBB4	TF binding region
ERBB4	CpG island
ENSG00000178568	chromatin interactions
ENSG00000201524	chromatin interactions

Extended variants
information (count: 1523 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1523 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113651000	chr2:213370709-213370710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs74501745	chr2:213370715-213370716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116142494	chr2:213370716-213370717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542051641	chr2:213370727-213370728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs76522327	chr2:213370754-213370755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368463454	chr2:213370768-213370769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575499065	chr2:213370806-213370807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545766386	chr2:213370824-213370825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575809442	chr2:213370840-213370841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375430939	chr2:213370853-213370854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552484660	chr2:213370875-213370876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370101263	chr2:213370876-213370877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571034220	chr2:213370878-213370879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111942710	chr2:213370893-213370894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540304448	chr2:213370928-213370929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562254587	chr2:213370994-213370995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529454778	chr2:213371016-213371017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551163140	chr2:213371037-213371038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6752016	chr2:213371066-213371067	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs371191520	chr2:213371073-213371074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs76451859	chr2:213371076-213371077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139118956	chr2:213371078-213371079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534652467	chr2:213371079-213371080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546368942	chr2:213371127-213371128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149869685	chr2:213371189-213371190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs386654832	chr2:213371236-213371237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372305093	chr2:213371244-213371245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570836627	chr2:213371256-213371257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79173357	chr2:213371258-213371259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575163672	chr2:213371276-213371277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539331137	chr2:213371291-213371292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540898545	chr2:213371297-213371298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557655390	chr2:213371376-213371377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs79624022	chr2:213371400-213371401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375263076	chr2:213371469-213371470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540270238	chr2:213371472-213371473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561999928	chr2:213371474-213371475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs114686372	chr2:213371508-213371509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs80274178	chr2:213371546-213371547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563083984	chr2:213371554-213371555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75114964	chr2:213371607-213371608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145104282	chr2:213371639-213371640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556881834	chr2:213371776-213371777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189885941	chr2:213371811-213371812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116269945	chr2:213371847-213371848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568036352	chr2:213371872-213371873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182485157	chr2:213371900-213371901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537942260	chr2:213371934-213371935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75037638	chr2:213371935-213371936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187044212	chr2:213371947-213371948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	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
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	21147756	CNVD
Schizophrenia	18990708	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:633 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213367800-213372200	Weak transcription	Aorta	Aorta
2	chr2:213370400-213373800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:213373800-213376000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:213376000-213376200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr2:213376200-213378600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:213378600-213378800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:213378800-213379000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr2:213379000-213380800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:213380800-213384400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:213381200-213381400	Enhancers	Brain Substantia Nigra	brain
11	chr2:213381200-213383000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:213381400-213382000	Weak transcription	Brain Substantia Nigra	brain
13	chr2:213381400-213384400	Enhancers	Fetal Heart	heart
14	chr2:213381600-213382400	Enhancers	Brain Anterior Caudate	brain
15	chr2:213382000-213382600	Enhancers	Brain Substantia Nigra	brain
16	chr2:213382600-213391800	Weak transcription	Brain Substantia Nigra	brain
17	chr2:213383000-213383400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:213383400-213383600	Enhancers	Aorta	Aorta
19	chr2:213383400-213383800	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr2:213383400-213384000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:213383600-213392200	Weak transcription	Aorta	Aorta
22	chr2:213383800-213388400	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr2:213384400-213384800	Weak transcription	Fetal Heart	heart
24	chr2:213384400-213395400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr2:213384800-213385800	Enhancers	Fetal Heart	heart
26	chr2:213385800-213386800	Weak transcription	Fetal Heart	heart
27	chr2:213386800-213390600	Enhancers	Fetal Heart	heart
28	chr2:213388400-213388800	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr2:213388800-213392800	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr2:213390600-213391600	Weak transcription	Fetal Heart	heart
31	chr2:213391600-213399200	Enhancers	Fetal Heart	heart
32	chr2:213391800-213392000	Enhancers	Brain Substantia Nigra	brain
33	chr2:213392000-213392800	Weak transcription	Brain Substantia Nigra	brain
34	chr2:213392200-213392800	Active TSS	Aorta	Aorta
35	chr2:213392600-213392800	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr2:213392600-213393200	Enhancers	Brain Hippocampus Middle	brain
37	chr2:213392800-213393000	Enhancers	Psoas Muscle	Psoas
38	chr2:213392800-213393000	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr2:213392800-213393200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr2:213392800-213393200	Flanking Active TSS	Aorta	Aorta
41	chr2:213392800-213393200	Flanking Active TSS	Brain Substantia Nigra	brain
42	chr2:213392800-213393200	Enhancers	Right Atrium	heart
43	chr2:213392800-213393200	Active TSS	Right Ventricle	heart
44	chr2:213392800-213393200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
45	chr2:213393000-213393200	Enhancers	Brain Angular Gyrus	brain
46	chr2:213393000-213393200	Enhancers	Brain Cingulate Gyrus	brain
47	chr2:213393000-213393600	Enhancers	Brain Anterior Caudate	brain
48	chr2:213393000-213399000	Weak transcription	Psoas Muscle	Psoas
49	chr2:213393000-213400800	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr2:213393200-213393600	Active TSS	Aorta	Aorta

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