Variant report

Variant	nsv875478
Chromosome Location	chr2:182960289-182998122
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:357)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:357 , 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	BRCA1	chr2:182997572-182998190	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr2:182993890-182994206	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr2:182967930-182968193	HepG2	liver:	n/a	chr2:182968079-182968090 chr2:182968079-182968092 chr2:182968123-182968134 chr2:182968080-182968091
4	CEBPB	chr2:182981661-182981727	K562	blood:	n/a	chr2:182981681-182981692
5	CEBPB	chr2:182967986-182968205	IMR90	lung:	n/a	chr2:182968079-182968090 chr2:182968079-182968092 chr2:182968123-182968134 chr2:182968080-182968091
6	CEBPB	chr2:182972550-182972815	HepG2	liver:	n/a	chr2:182972667-182972678
7	CEBPB	chr2:182981540-182981834	IMR90	lung:	n/a	chr2:182981681-182981692
8	CEBPB	chr2:182981597-182981861	HepG2	liver:	n/a	chr2:182981681-182981692
9	CTCF	chr2:182966100-182966250	GM12875	blood:	n/a	chr2:182966165-182966186
10	CTCF	chr2:182997360-182997678	MCF-7	breast:	n/a	n/a
11	CTCF	chr2:182997440-182997590	GM12873	blood:	n/a	n/a
12	CTCF	chr2:182966140-182966290	NB4	blood:	n/a	chr2:182966165-182966186
13	CTCF	chr2:182997460-182997610	HUVEC	blood vessel:	n/a	n/a
14	CTCF	chr2:182966120-182966270	GM12867	blood:	n/a	chr2:182966165-182966186
15	CTCF	chr2:182997482-182997574	MCF-7	breast:	n/a	n/a
16	CTCF	chr2:182997440-182997590	HRE	kidney:	n/a	n/a
17	CTCF	chr2:182966160-182966310	HPAF	blood vessel:	n/a	chr2:182966165-182966186
18	CTCF	chr2:182966160-182966310	HepG2	liver:	n/a	chr2:182966165-182966186
19	CTCF	chr2:182966120-182966270	SAEC	small airway:	n/a	chr2:182966165-182966186
20	CTCF	chr2:182997420-182997570	HRE	kidney:	n/a	n/a
21	CTCF	chr2:182997480-182997630	HMEC	breast:	n/a	n/a
22	CTCF	chr2:182997440-182997590	HRPEpiC	eye:	n/a	n/a
23	CTCF	chr2:182966200-182966350	AG04450	lung:	n/a	n/a
24	CTCF	chr2:182966093-182966256	K562	blood:	n/a	chr2:182966165-182966186
25	CTCF	chr2:182997460-182997610	HEEpiC	esophagus:	n/a	n/a
26	CTCF	chr2:182966120-182966270	GM12864	blood:	n/a	chr2:182966165-182966186
27	CTCF	chr2:182997469-182997591	Pancreas_OC	pancreas:	n/a	n/a
28	CTCF	chr2:182966200-182966350	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr2:182968260-182968410	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr2:182965820-182965970	AG04449	skin:	n/a	n/a
31	CTCF	chr2:182968280-182968430	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr2:182997500-182997650	HFF-Myc	foreskin:	n/a	n/a
33	CTCF	chr2:182997460-182997610	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr2:182966100-182966250	HCPEpiC	choroid plexus:	n/a	chr2:182966165-182966186
35	CTCF	chr2:182997263-182997816	HCT-116	colon:	n/a	n/a
36	CTCF	chr2:182966060-182966210	Caco-2	colon:	n/a	chr2:182966165-182966186
37	CTCF	chr2:182966080-182966230	GM12872	blood:	n/a	chr2:182966165-182966186
38	CTCF	chr2:182966460-182966610	GM12872	blood:	n/a	n/a
39	CTCF	chr2:182965940-182966090	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr2:182997500-182997650	HAc	cerebellar:	n/a	n/a
41	CTCF	chr2:182997460-182997610	AG04450	lung:	n/a	n/a
42	CTCF	chr2:182997457-182997569	HepG2	liver:	n/a	n/a
43	CTCF	chr2:182974420-182974570	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr2:182966140-182966290	K562	blood:	n/a	chr2:182966165-182966186
45	CTCF	chr2:182997520-182997670	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr2:182966020-182966170	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr2:182966254-182966260	HepG2	liver:	n/a	n/a
48	CTCF	chr2:182966120-182966270	BE2_C	brain:	n/a	chr2:182966165-182966186
49	CTCF	chr2:182966240-182966390	GM06990	blood:	n/a	n/a
50	CTCF	chr2:182966100-182966250	HMF	breast:	n/a	chr2:182966165-182966186

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:182982011-182982061	NH-A	brain:	n/a
2	chr2:182982011-182982061	A549	lung:	n/a
3	chr2:182982011-182982061	HCM	heart:	n/a
4	chr2:182982011-182982061	LNCaP	prostate:	n/a
5	chr2:182982011-182982061	U87	brain:	n/a
6	chr2:182982011-182982061	H1-hESC	embryonic stem cell:	embryo
7	chr2:182982011-182982061	GM19239	blood:	n/a
8	chr2:182982011-182982061	ECC-1	luminal epithelium:	n/a
9	chr2:182982011-182982061	HRPEpiC	eye:	n/a
10	chr2:182982011-182982061	SAEC	small airway:	n/a
11	chr2:182982011-182982061	Jurkat	blood:	n/a
12	chr2:182982011-182982061	HUVEC	blood vessel:	n/a
13	chr2:182982011-182982061	HRE	kidney:	n/a
14	chr2:182982011-182982061	Hepatocyte	liver:	n/a
15	chr2:182982011-182982061	HCF	heart:	n/a
16	chr2:182982011-182982061	AG09309	skin:	n/a
17	chr2:182982011-182982061	HEK293	kidney:	embryo
18	chr2:182982011-182982061	NHDF-neo	bronchial:	n/a
19	chr2:182982011-182982061	PANC-1	pancreas:	n/a
20	chr2:182982011-182982061	ovcar-3	ovarian:	n/a
21	chr2:182982011-182982061	ProgFib	skin:	n/a
22	chr2:182982011-182982061	CMK	blood:	n/a
23	chr2:182982011-182982061	SK-N-SH	brain:	n/a
24	chr2:182982011-182982061	MCF10A-Er-Src	breast:	n/a
25	chr2:182982011-182982061	GM06990	blood:	n/a
26	chr2:182982011-182982061	AG04450	lung:	fetal
27	chr2:182982011-182982061	HCT-116	colon:	n/a
28	chr2:182982011-182982061	PrEC	prostate:	n/a
29	chr2:182982011-182982061	SK-N-SH_RA	brain:	n/a
30	chr2:182982011-182982061	K562	blood:	n/a
31	chr2:182982011-182982061	HNPCEpiC	eye:	n/a
32	chr2:182982011-182982061	GM12891	blood:	n/a
33	chr2:182982011-182982061	HIPEpiC	eye:	n/a
34	chr2:182982011-182982061	NHBE	bronchial:	n/a
35	chr2:182982011-182982061	Hela-S3	cervix:	n/a
36	chr2:182982011-182982061	AG04449	skin:	fetal
37	chr2:182982011-182982061	NB4	blood:	n/a
38	chr2:182982011-182982061	GM12892	blood:	n/a
39	chr2:182982011-182982061	BE2_C	brain:	n/a
40	chr2:182982011-182982061	HRCEpiC	kidney:	n/a
41	chr2:182982011-182982061	SK-N-MC	brain:	n/a
42	chr2:182982011-182982061	HMEC	breast:	n/a
43	chr2:182982011-182982061	MCF-7	breast:	n/a
44	chr2:182982011-182982061	AG10803	skin:	n/a
45	chr2:182982011-182982061	T-47D	breast:	n/a
46	chr2:182982011-182982061	HEEpiC	esophagus:	n/a
47	chr2:182982011-182982061	Caco-2	colon:	n/a
48	chr2:182982011-182982061	AG09319	gingival:	n/a
49	chr2:182982011-182982061	GM12878	blood:	n/a
50	chr2:182982011-182982061	AoSMC	blood vessel:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:182760625..182763204-chr2:182996847..182998737,3	MCF-7	breast:
2	chr2:182759435..182761686-chr2:182994619..182996651,2	MCF-7	breast:
3	chr2:182976792..182978439-chr2:182980640..182982380,2	K562	blood:
4	chr2:182955166..182957496-chr2:182959332..182961778,2	K562	blood:
5	chr2:182780940..182782752-chr2:182991340..182994211,2	MCF-7	breast:
6	chr2:182607039..182609775-chr2:182996269..182999208,3	MCF-7	breast:
7	chr2:62082104..62083680-chr2:182961228..182962748,2	MCF-7	breast:
8	chr2:182754959..182757996-chr2:182990661..182994349,5	MCF-7	breast:
9	chr2:182438221..182439821-chr2:182994144..182995776,2	MCF-7	breast:
10	chr2:182948523..182950628-chr2:182991331..182993046,3	MCF-7	breast:
11	chr2:182976792..182978439-chr2:182980640..182982380,2	K562	blood:
12	chr2:182940136..182945901-chr2:182990915..182998605,17	MCF-7	breast:
13	chr2:182971673..182974149-chr2:182975000..182977579,2	K562	blood:
14	chr2:182941653..182947128-chr2:182990854..182994247,10	MCF-7	breast:
15	chr2:182759840..182761573-chr2:182989686..182991505,2	MCF-7	breast:
16	chr2:182756103..182758959-chr2:182990801..182994027,3	MCF-7	breast:
17	chr2:182607320..182608150-chr2:182997133..182997648,2	MCF-7	breast:
18	chr2:182437539..182438523-chr2:182997112..182997742,2	MCF-7	breast:
19	chr2:182943387..182944241-chr2:182990575..182991501,3	MCF-7	breast:
20	chr2:182942463..182945440-chr2:182995161..182998579,4	MCF-7	breast:
21	chr2:182817707..182819677-chr2:182989420..182992160,2	MCF-7	breast:
22	chr2:182943646..182944243-chr2:182990884..182991578,2	MCF-7	breast:
23	chr2:182943249..182944272-chr2:182991017..182991773,5	MCF-7	breast:
24	chr2:182765593..182767141-chr2:182997706..182999460,2	MCF-7	breast:
25	chr2:182816967..182818729-chr2:182991457..182992966,2	MCF-7	breast:
26	chr2:182884188..182888119-chr2:182990048..182995139,6	MCF-7	breast:
27	chr2:182754700..182758987-chr2:182995578..182999206,6	MCF-7	breast:
28	chr2:182608371..182610484-chr2:182990865..182992753,2	MCF-7	breast:
29	chr2:182971673..182974149-chr2:182975000..182977579,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SSFA2-1	chr2:182991664-182993417	NONHSAT075904

No data

Variant related genes	Relation type
PPP1R1C	TF binding region
PPP1R1C	CpG island
ENSG00000150722	chromatin interactions
ENSG00000260742	chromatin interactions
ENSG00000138434	chromatin interactions

Extended variants
information (count: 1470 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:1470 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16822550	chr2:182960289-182960290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372019896	chr2:182960316-182960317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555885105	chr2:182960319-182960320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547351726	chr2:182960354-182960355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533990712	chr2:182960378-182960379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1107901	chr2:182960414-182960415	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs541841245	chr2:182960421-182960422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555038779	chr2:182960424-182960425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114677306	chr2:182960445-182960446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542606524	chr2:182960478-182960479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1107902	chr2:182960485-182960486	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs564278507	chr2:182960523-182960524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577959517	chr2:182960588-182960589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185008337	chr2:182960649-182960650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563034081	chr2:182960656-182960657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575846900	chr2:182960657-182960658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531690078	chr2:182960667-182960668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149092440	chr2:182960682-182960683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561900458	chr2:182960685-182960686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs115379809	chr2:182960697-182960698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78514119	chr2:182960709-182960710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570805180	chr2:182960711-182960712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143115094	chr2:182960713-182960714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35074121	chr2:182960722-182960723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577168446	chr2:182960723-182960724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs397785436	chr2:182960736-182960737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564508602	chr2:182960759-182960760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533534250	chr2:182960813-182960814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375179589	chr2:182960887-182960888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540448328	chr2:182960958-182960959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560172447	chr2:182960999-182961000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189272181	chr2:182961009-182961010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529388052	chr2:182961011-182961012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555354649	chr2:182961060-182961061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1515891	chr2:182961100-182961101	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs148276504	chr2:182961132-182961133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141302795	chr2:182961133-182961134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371444097	chr2:182961134-182961135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150826017	chr2:182961142-182961143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531489069	chr2:182961169-182961170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543670241	chr2:182961171-182961172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10669358	chr2:182961174-182961175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373562545	chr2:182961178-182961179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576495543	chr2:182961179-182961180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541917981	chr2:182961256-182961257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113389485	chr2:182961260-182961261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs138344046	chr2:182961261-182961262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs1515892	chr2:182961270-182961271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs1400003	chr2:182961271-182961272	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs143827353	chr2:182961273-182961274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	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
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:131 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182954200-182968200	Weak transcription	Psoas Muscle	Psoas
2	chr2:182958200-182969800	Weak transcription	Thymus	Thymus
3	chr2:182960200-182961400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:182961200-182961600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr2:182961400-182961600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr2:182961600-182962200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:182962200-182962400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:182962200-182964000	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr2:182962400-182967600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr2:182962600-182963200	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr2:182963400-182964200	Enhancers	Fetal Intestine Large	intestine
12	chr2:182965400-182965800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:182965400-182966600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:182965600-182966600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr2:182965800-182966400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr2:182965800-182968600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:182966000-182966600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr2:182966000-182966600	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr2:182966200-182966400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr2:182966200-182966600	Enhancers	H1 Cell Line	embryonic stem cell
21	chr2:182966200-182966600	Enhancers	H9 Cell Line	embryonic stem cell
22	chr2:182966200-182966800	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr2:182966200-182966800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr2:182966400-182966800	Enhancers	Fetal Thymus	thymus
25	chr2:182966600-182968200	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr2:182966600-182970800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:182966800-182968200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr2:182966800-182968200	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr2:182966800-182996400	Weak transcription	Fetal Thymus	thymus
30	chr2:182967600-182969400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr2:182968000-182968600	Enhancers	Brain Substantia Nigra	brain
32	chr2:182968200-182968400	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr2:182968200-182968400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr2:182968200-182968400	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr2:182968200-182968400	Enhancers	Psoas Muscle	Psoas
36	chr2:182968200-182968600	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr2:182968200-182968800	Enhancers	Brain Anterior Caudate	brain
38	chr2:182968200-182969000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr2:182968200-182969000	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr2:182968400-182970800	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr2:182968600-182969000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:182968600-182969000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr2:182974000-182975200	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr2:182974400-182975200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr2:182974400-182975600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr2:182974400-182975800	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr2:182975200-182975400	Enhancers	Left Ventricle	heart
48	chr2:182975200-182975600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr2:182975200-182975600	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr2:182975200-182975600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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