Variant report

Variant	nsv1014680
Chromosome Location	chr2:213142147-213301614
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:469)
CpG islands
(count:183)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:213288860-213289080	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:213224153-213224545	HepG2	liver:	n/a	n/a
3	ATF2	chr2:213164628-213165033	GM12878	blood:	n/a	n/a
4	BCL11A	chr2:213293765-213294070	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr2:213164643-213165029	GM12878	blood:	n/a	chr2:213164727-213164736
6	BCL11A	chr2:213164602-213165058	GM12878	blood:	n/a	chr2:213164727-213164736
7	BHLHE40	chr2:213164655-213165134	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:213224318-213224388	HepG2	liver:	n/a	n/a
9	CCNT2	chr2:213167804-213168004	K562	blood:	n/a	n/a
10	CEBPB	chr2:213253278-213253564	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:213192968-213193202	A549	lung:	n/a	chr2:213193066-213193077
12	CEBPB	chr2:213240564-213240940	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:213209262-213209565	IMR90	lung:	n/a	chr2:213209320-213209329 chr2:213209437-213209454 chr2:213209320-213209329 chr2:213209442-213209453 chr2:213209440-213209451
14	CEBPB	chr2:213209362-213209592	HepG2	liver:	n/a	chr2:213209437-213209454 chr2:213209442-213209453 chr2:213209440-213209451
15	CEBPB	chr2:213224251-213224578	HepG2	liver:	n/a	chr2:213224544-213224556
16	CEBPB	chr2:213155653-213155877	HepG2	liver:	n/a	chr2:213155792-213155803 chr2:213155790-213155801 chr2:213155790-213155803
17	CEBPB	chr2:213286777-213287045	A549	lung:	n/a	n/a
18	CEBPB	chr2:213240458-213240973	A549	lung:	n/a	n/a
19	CEBPB	chr2:213165371-213165600	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:213240450-213241002	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:213209329-213209566	A549	lung:	n/a	chr2:213209437-213209454 chr2:213209442-213209453 chr2:213209440-213209451
22	CEBPB	chr2:213192916-213193235	IMR90	lung:	n/a	chr2:213193066-213193077
23	CEBPB	chr2:213240595-213240973	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr2:213192901-213193253	HepG2	liver:	n/a	chr2:213193066-213193077
25	CEBPB	chr2:213165459-213165613	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr2:213271036-213271238	HepG2	liver:	n/a	chr2:213271134-213271147
27	CEBPB	chr2:213209433-213209436	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr2:213164541-213165145	GM12878	blood:	n/a	n/a
29	CTCF	chr2:213161460-213161610	GM12875	blood:	n/a	n/a
30	CTCF	chr2:213188780-213188930	GM12865	blood:	n/a	n/a
31	CTCF	chr2:213267160-213267310	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr2:213267159-213267287	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr2:213142140-213142290	Caco-2	colon:	n/a	n/a
34	CTCF	chr2:213267120-213267270	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr2:213267220-213267370	AG10803	skin:	n/a	n/a
36	CTCF	chr2:213267052-213267430	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:213267180-213267330	AG10803	skin:	n/a	n/a
38	CTCF	chr2:213267140-213267290	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:213267160-213267353	LNCaP	prostate:	n/a	n/a
40	CTCF	chr2:213196867-213196975	GM20000	blood:	n/a	n/a
41	CTCF	chr2:213195020-213195170	BE2_C	brain:	n/a	n/a
42	CTCF	chr2:213267123-213267325	GM12878	blood:	n/a	n/a
43	CTCF	chr2:213289000-213289150	HEK293	kidney:	n/a	n/a
44	CTCF	chr2:213289020-213289170	HCT-116	colon:	n/a	n/a
45	CTCF	chr2:213160480-213160630	HepG2	liver:	n/a	n/a
46	CTCF	chr2:213286680-213286830	AG10803	skin:	n/a	n/a
47	CTCF	chr2:213289002-213289100	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr2:213267100-213267250	AG09309	skin:	n/a	n/a
49	CTCF	chr2:213267160-213267310	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr2:213267198-213267247	LNCaP	prostate:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:213248884-213248934	U87	brain:	n/a
2	chr2:213248884-213248934	AG04449	skin:	fetal
3	chr2:213248884-213248934	AG04450	lung:	fetal
4	chr2:213228956-213229006	HMEC	breast:	n/a
5	chr2:213228956-213229006	HNPCEpiC	eye:	n/a
6	chr2:213228956-213229006	ovcar-3	ovarian:	n/a
7	chr2:213228956-213229006	GM12892	blood:	n/a
8	chr2:213228956-213229006	AG04450	lung:	fetal
9	chr2:213292541-213292591	CMK	blood:	n/a
10	chr2:213292541-213292591	HNPCEpiC	eye:	n/a
11	chr2:213292541-213292591	AG09309	skin:	n/a
12	chr2:213228956-213229006	GM19239	blood:	n/a
13	chr2:213248884-213248934	HRPEpiC	eye:	n/a
14	chr2:213292541-213292591	PFSK-1	brain:	n/a
15	chr2:213228956-213229006	LNCaP	prostate:	n/a
16	chr2:213248884-213248934	HAEpiC	amniotic membrane:	n/a
17	chr2:213292541-213292591	K562	blood:	n/a
18	chr2:213292541-213292591	HEEpiC	esophagus:	n/a
19	chr2:213292541-213292591	HRE	kidney:	n/a
20	chr2:213248884-213248934	GM19239	blood:	n/a
21	chr2:213228956-213229006	PFSK-1	brain:	n/a
22	chr2:213228956-213229006	HCPEpiC	choroid plexus:	n/a
23	chr2:213248884-213248934	ECC-1	luminal epithelium:	n/a
24	chr2:213228956-213229006	HL-60	blood:	n/a
25	chr2:213292541-213292591	NHDF-neo	bronchial:	n/a
26	chr2:213228956-213229006	HRCEpiC	kidney:	n/a
27	chr2:213292541-213292591	GM19239	blood:	n/a
28	chr2:213248884-213248934	A549	lung:	n/a
29	chr2:213228956-213229006	HRE	kidney:	n/a
30	chr2:213248884-213248934	SAEC	small airway:	n/a
31	chr2:213248884-213248934	PANC-1	pancreas:	n/a
32	chr2:213248884-213248934	SK-N-SH_RA	brain:	n/a
33	chr2:213228956-213229006	HepG2	liver:	n/a
34	chr2:213228956-213229006	NH-A	brain:	n/a
35	chr2:213228956-213229006	HEK293	kidney:	embryo
36	chr2:213292541-213292591	IMR90	lung:	fetal
37	chr2:213228956-213229006	Hela-S3	cervix:	n/a
38	chr2:213228956-213229006	ECC-1	luminal epithelium:	n/a
39	chr2:213248884-213248934	MCF10A-Er-Src	breast:	n/a
40	chr2:213292541-213292591	GM06990	blood:	n/a
41	chr2:213248884-213248934	BE2_C	brain:	n/a
42	chr2:213292541-213292591	GM12891	blood:	n/a
43	chr2:213292541-213292591	SKMC	muscle:	n/a
44	chr2:213292541-213292591	AoSMC	blood vessel:	n/a
45	chr2:213228956-213229006	GM06990	blood:	n/a
46	chr2:213228956-213229006	Jurkat	blood:	n/a
47	chr2:213248884-213248934	HMEC	breast:	n/a
48	chr2:213228956-213229006	NB4	blood:	n/a
49	chr2:213248884-213248934	T-47D	breast:	n/a
50	chr2:213228956-213229006	U87	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:213294886..213296406-chrX:142860992..142862514,2	K562	blood:
2	chr2:213169330..213171305-chr2:213174705..213177385,2	MCF-7	breast:
3	chr2:213213790..213216008-chr2:213223245..213225984,2	MCF-7	breast:
4	chr2:213213790..213216008-chr2:213223245..213225984,2	MCF-7	breast:
5	chr2:213169330..213171305-chr2:213174705..213177385,2	MCF-7	breast:
6	chr2:213169267..213171740-chr2:213191721..213193864,2	MCF-7	breast:
7	chr2:213280702..213283541-chr2:213286415..213289040,2	MCF-7	breast:
8	chr2:213223218..213224821-chr2:213227410..213229033,2	MCF-7	breast:
9	chr2:213252657..213254943-chr2:213260775..213262754,2	K562	blood:
10	chr2:213280702..213283541-chr2:213286415..213289040,2	MCF-7	breast:
11	chr2:213202563..213204297-chr2:213206010..213208677,2	K562	blood:
12	chr2:213169267..213171740-chr2:213191721..213193864,2	MCF-7	breast:
13	chr2:213223218..213224821-chr2:213227410..213229033,2	MCF-7	breast:
14	chr2:213165115..213165752-chr21:42883583..42884373,2	MCF-7	breast:
15	chr2:213145552..213149044-chr2:213151103..213154081,3	MCF-7	breast:
16	chr2:213217638..213221383-chr2:213223310..213226579,3	MCF-7	breast:
17	chr2:213202563..213204297-chr2:213206010..213208677,2	K562	blood:
18	chr2:213145552..213149044-chr2:213151103..213154081,3	MCF-7	breast:
19	chr2:213217638..213221383-chr2:213223310..213226579,3	MCF-7	breast:
20	chr2:213252657..213254943-chr2:213260775..213262754,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548f-3p	chr2:213291008-213291026	MIMAT0005895_1

No data

Variant related genes	Relation type
MIR548F2	TF binding region
ERBB4	TF binding region
MIR548F2	CpG island
ERBB4	CpG island

Extended variants
information (count: 5780 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:5780 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114388700	chr2:213142151-213142152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs79233971	chr2:213142172-213142173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546094713	chr2:213142231-213142232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575271651	chr2:213142241-213142242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs377349040	chr2:213142248-213142249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs76263877	chr2:213142264-213142265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574684175	chr2:213142326-213142327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs111922497	chr2:213142355-213142356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138500273	chr2:213142369-213142370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370689158	chr2:213142394-213142395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560433390	chr2:213142419-213142420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192137278	chr2:213142428-213142429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185384394	chr2:213142467-213142468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190312092	chr2:213142480-213142481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs193271355	chr2:213142511-213142512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548173510	chr2:213142512-213142513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561487108	chr2:213142602-213142603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs80326718	chr2:213142630-213142631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138371137	chr2:213142674-213142675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559158050	chr2:213142714-213142715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs55872057	chr2:213142732-213142733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566754365	chr2:213142746-213142747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113354045	chr2:213142792-213142793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532554814	chr2:213142805-213142806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149263156	chr2:213142815-213142816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569357209	chr2:213142839-213142840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537910312	chr2:213142912-213142913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs77101837	chr2:213142940-213142941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568358440	chr2:213142981-213142982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112517958	chr2:213143019-213143020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537587011	chr2:213143033-213143034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554093045	chr2:213143045-213143046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577175058	chr2:213143079-213143080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548073433	chr2:213143080-213143081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143452129	chr2:213143140-213143141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556346911	chr2:213143147-213143148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73066369	chr2:213143151-213143152	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs114609408	chr2:213143171-213143172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561769541	chr2:213143204-213143205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527272970	chr2:213143254-213143255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112836883	chr2:213143257-213143258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34560702	chr2:213143266-213143267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13002202	chr2:213143285-213143286	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs560431085	chr2:213143303-213143304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs17346524	chr2:213143316-213143317	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs188175374	chr2:213143349-213143350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs367695175	chr2:213143392-213143393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552361582	chr2:213143436-213143437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs137858951	chr2:213143442-213143443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181061676	chr2:213143456-213143457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Pancreatic cancer	17952125	CNVD
Schizophrenia	18990708	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:632 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213134200-213145200	Weak transcription	Aorta	Aorta
2	chr2:213134400-213147400	Weak transcription	Brain Substantia Nigra	brain
3	chr2:213136600-213147400	Weak transcription	Psoas Muscle	Psoas
4	chr2:213139200-213145400	Weak transcription	Fetal Heart	heart
5	chr2:213139200-213146200	Weak transcription	Brain Hippocampus Middle	brain
6	chr2:213141800-213147400	Weak transcription	Brain Anterior Caudate	brain
7	chr2:213142000-213147200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:213145200-213145600	Enhancers	Aorta	Aorta
9	chr2:213145400-213145600	Enhancers	Fetal Heart	heart
10	chr2:213145600-213146000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr2:213145600-213146000	Weak transcription	Fetal Heart	heart
12	chr2:213145600-213146800	Weak transcription	Aorta	Aorta
13	chr2:213146000-213149400	Enhancers	Fetal Heart	heart
14	chr2:213146200-213150200	Enhancers	Brain Hippocampus Middle	brain
15	chr2:213146400-213146800	Enhancers	Brain Angular Gyrus	brain
16	chr2:213146800-213147200	Active TSS	Aorta	Aorta
17	chr2:213146800-213148400	Enhancers	Brain Cingulate Gyrus	brain
18	chr2:213146800-213149000	Weak transcription	Brain Angular Gyrus	brain
19	chr2:213146800-213149600	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr2:213147200-213147800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr2:213147200-213148000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr2:213147200-213148200	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr2:213147200-213149000	Weak transcription	Aorta	Aorta
24	chr2:213147400-213147800	Enhancers	Brain Substantia Nigra	brain
25	chr2:213147400-213148000	Enhancers	Psoas Muscle	Psoas
26	chr2:213147400-213148400	Enhancers	Brain Anterior Caudate	brain
27	chr2:213147600-213148000	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr2:213147800-213148200	Enhancers	Brain Germinal Matrix	brain
29	chr2:213147800-213148200	Flanking Active TSS	Brain Substantia Nigra	brain
30	chr2:213147800-213148800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr2:213148000-213148200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr2:213148000-213149000	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr2:213148000-213149000	Weak transcription	Psoas Muscle	Psoas
34	chr2:213148000-213155000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr2:213148200-213150000	Enhancers	Brain Substantia Nigra	brain
36	chr2:213148400-213149000	Weak transcription	Brain Cingulate Gyrus	brain
37	chr2:213148400-213149200	Weak transcription	Brain Anterior Caudate	brain
38	chr2:213148600-213149000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr2:213148600-213150000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr2:213148800-213149000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
41	chr2:213148800-213149200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr2:213149000-213149200	Enhancers	Aorta	Aorta
43	chr2:213149000-213149200	Enhancers	Brain Cingulate Gyrus	brain
44	chr2:213149000-213149200	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr2:213149000-213149400	Enhancers	Psoas Muscle	Psoas
46	chr2:213149000-213149600	Enhancers	Fetal Kidney	kidney
47	chr2:213149000-213149800	Enhancers	Brain Angular Gyrus	brain
48	chr2:213149200-213150000	Weak transcription	Aorta	Aorta
49	chr2:213149200-213150000	Enhancers	Brain Anterior Caudate	brain
50	chr2:213149400-213149800	Weak transcription	Fetal Heart	heart

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