Variant report

Variant	nsv516644
Chromosome Location	chr2:134301130-134391214
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:134334204-134334594	HepG2	liver:	n/a	n/a
2	ATF1	chr2:134318802-134318942	K562	blood:	n/a	n/a
3	BHLHE40	chr2:134348127-134348457	GM12878	blood:	n/a	n/a
4	BHLHE40	chr2:134348631-134349043	HepG2	liver:	n/a	chr2:134348906-134348915 chr2:134348907-134348916 chr2:134348907-134348916 chr2:134348901-134348922 chr2:134348908-134348917
5	BHLHE40	chr2:134348833-134349033	K562	blood:	n/a	chr2:134348906-134348915 chr2:134348907-134348916 chr2:134348907-134348916 chr2:134348901-134348922 chr2:134348908-134348917
6	BHLHE40	chr2:134318760-134318986	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:134357949-134358221	HepG2	liver:	n/a	chr2:134358076-134358085 chr2:134358075-134358084 chr2:134358075-134358084 chr2:134358069-134358090 chr2:134358073-134358086
8	CEBPB	chr2:134360722-134360943	IMR90	lung:	n/a	chr2:134360853-134360864
9	CEBPB	chr2:134382622-134382822	Hela-S3	cervix:	n/a	chr2:134382703-134382714 chr2:134382702-134382715
10	CEBPB	chr2:134382552-134382837	A549	lung:	n/a	chr2:134382703-134382714 chr2:134382702-134382715
11	CEBPB	chr2:134346210-134346223	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:134345620-134345801	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:134360733-134360971	A549	lung:	n/a	chr2:134360853-134360864
14	CEBPB	chr2:134363005-134363306	IMR90	lung:	n/a	chr2:134363162-134363175
15	CEBPB	chr2:134382554-134382834	IMR90	lung:	n/a	chr2:134382703-134382714 chr2:134382702-134382715
16	CEBPB	chr2:134349676-134350255	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr2:134356692-134356729	A549	lung:	n/a	n/a
18	CEBPB	chr2:134360678-134360981	HepG2	liver:	n/a	chr2:134360853-134360864
19	CEBPB	chr2:134339549-134339813	HepG2	liver:	n/a	chr2:134339553-134339565 chr2:134339691-134339702
20	CEBPB	chr2:134382543-134382851	HepG2	liver:	n/a	chr2:134382703-134382714 chr2:134382702-134382715
21	CEBPB	chr2:134324586-134324858	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:134345597-134345824	IMR90	lung:	n/a	n/a
23	CEBPB	chr2:134360675-134360978	MCF-7	breast:	n/a	chr2:134360853-134360864
24	CEBPB	chr2:134356823-134357160	HepG2	liver:	n/a	chr2:134356993-134357004 chr2:134357074-134357082
25	CEBPB	chr2:134360801-134360871	Hela-S3	cervix:	n/a	chr2:134360853-134360864
26	CEBPB	chr2:134352377-134352446	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:134338548-134338862	IMR90	lung:	n/a	n/a
28	CEBPB	chr2:134360831-134360922	H1-hESC	embryonic stem cell:	n/a	chr2:134360853-134360864
29	CTCF	chr2:134389646-134389805	MCF-7	breast:	n/a	chr2:134389791-134389804 chr2:134389711-134389721 chr2:134389706-134389724
30	CTCF	chr2:134322560-134322710	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr2:134318740-134318890	AoAF	blood vessel:	n/a	chr2:134318811-134318829 chr2:134318806-134318827
32	CTCF	chr2:134339040-134339190	HepG2	liver:	n/a	n/a
33	CTCF	chr2:134318760-134318910	GM12868	blood:	n/a	chr2:134318811-134318829 chr2:134318806-134318827
34	CTCF	chr2:134318618-134319037	GM12878	blood:	n/a	chr2:134318811-134318829 chr2:134318806-134318827
35	CTCF	chr2:134318720-134318870	HUVEC	blood vessel:	n/a	chr2:134318811-134318829 chr2:134318806-134318827
36	CTCF	chr2:134339000-134339150	GM12872	blood:	n/a	n/a
37	CTCF	chr2:134318740-134318890	HMF	breast:	n/a	chr2:134318811-134318829 chr2:134318806-134318827
38	CTCF	chr2:134339049-134339126	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:134318740-134318890	GM12874	blood:	n/a	chr2:134318811-134318829 chr2:134318806-134318827
40	CTCF	chr2:134348900-134349050	AG10803	skin:	n/a	n/a
41	CTCF	chr2:134318720-134318870	HRE	kidney:	n/a	chr2:134318811-134318829 chr2:134318806-134318827
42	CTCF	chr2:134318740-134318890	AG09309	skin:	n/a	chr2:134318811-134318829 chr2:134318806-134318827
43	CTCF	chr2:134318734-134318913	GM10248	blood:	n/a	chr2:134318811-134318829 chr2:134318806-134318827
44	CTCF	chr2:134389620-134389770	BE2_C	brain:	n/a	chr2:134389711-134389721 chr2:134389706-134389724
45	CTCF	chr2:134318780-134318930	GM12869	blood:	n/a	chr2:134318811-134318829 chr2:134318806-134318827
46	CTCF	chr2:134318760-134318910	HAc	cerebellar:	n/a	chr2:134318811-134318829 chr2:134318806-134318827
47	CTCF	chr2:134318720-134318870	AoAF	blood vessel:	n/a	chr2:134318811-134318829 chr2:134318806-134318827
48	CTCF	chr2:134318665-134318998	HUVEC	blood vessel:	n/a	chr2:134318811-134318829 chr2:134318806-134318827
49	CTCF	chr2:134318760-134318910	BJ	skin:	n/a	chr2:134318811-134318829 chr2:134318806-134318827
50	CTCF	chr2:134348820-134348970	AG04450	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:134333275-134333325	SK-N-SH	brain:	n/a
2	chr2:134347783-134347833	HUVEC	blood vessel:	n/a
3	chr2:134333275-134333325	SK-N-SH	brain:	n/a
4	chr2:134347783-134347833	HUVEC	blood vessel:	n/a
5	chr2:134326172-134326222	A549	lung:	n/a
6	chr2:134304756-134304806	PANC-1	pancreas:	n/a
7	chr2:134326273-134326323	PANC-1	pancreas:	n/a
8	chr2:134318278-134318328	HEEpiC	esophagus:	n/a
9	chr2:134329911-134329961	MCF10A-Er-Src	breast:	n/a
10	chr2:134326913-134326963	HMEC	breast:	n/a
11	chr2:134326366-134326416	HRCEpiC	kidney:	n/a
12	chr2:134347783-134347833	PANC-1	pancreas:	n/a
13	chr2:134326017-134326067	HMEC	breast:	n/a
14	chr2:134329911-134329961	K562	blood:	n/a
15	chr2:134304756-134304806	Jurkat	blood:	n/a
16	chr2:134329911-134329961	PrEC	prostate:	n/a
17	chr2:134304756-134304806	RPTEC	kidney:	n/a
18	chr2:134333275-134333325	GM12891	blood:	n/a
19	chr2:134326273-134326323	AG04449	skin:	fetal
20	chr2:134347783-134347833	ECC-1	luminal epithelium:	n/a
21	chr2:134325873-134325923	NHBE	bronchial:	n/a
22	chr2:134326204-134326254	HepG2	liver:	n/a
23	chr2:134326913-134326963	HCPEpiC	choroid plexus:	n/a
24	chr2:134326366-134326416	NT2-D1	testis:	n/a
25	chr2:134324896-134324946	HMEC	breast:	n/a
26	chr2:134326055-134326105	Hela-S3	cervix:	n/a
27	chr2:134326204-134326254	T-47D	breast:	n/a
28	chr2:134325873-134325923	NB4	blood:	n/a
29	chr2:134318278-134318328	MCF-7	breast:	n/a
30	chr2:134329911-134329961	SK-N-MC	brain:	n/a
31	chr2:134326172-134326222	HEK293	kidney:	embryo
32	chr2:134304653-134304703	MCF-7	breast:	n/a
33	chr2:134326273-134326323	HCT-116	colon:	n/a
34	chr2:134326204-134326254	AG09319	gingival:	n/a
35	chr2:134304653-134304703	GM12891	blood:	n/a
36	chr2:134304756-134304806	HAEpiC	amniotic membrane:	n/a
37	chr2:134357740-134357790	CMK	blood:	n/a
38	chr2:134357740-134357790	AG10803	skin:	n/a
39	chr2:134333275-134333325	HIPEpiC	eye:	n/a
40	chr2:134304756-134304806	Hela-S3	cervix:	n/a
41	chr2:134325873-134325923	AG10803	skin:	n/a
42	chr2:134360386-134360436	HRE	kidney:	n/a
43	chr2:134326204-134326254	GM12878	blood:	n/a
44	chr2:134347783-134347833	GM12891	blood:	n/a
45	chr2:134326366-134326416	Jurkat	blood:	n/a
46	chr2:134368695-134368745	NB4	blood:	n/a
47	chr2:134326017-134326067	AG04449	skin:	fetal
48	chr2:134325873-134325923	GM06990	blood:	n/a
49	chr2:134326017-134326067	AG09319	gingival:	n/a
50	chr2:134304653-134304703	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:134317975..134320308-chr2:134325605..134328573,2	MCF-7	breast:
2	chr1:115534913..115537064-chr2:134331546..134333368,2	MCF-7	breast:
3	chr2:134325568..134327875-chr2:134328261..134331038,2	MCF-7	breast:
4	chr2:133106241..133106888-chr2:134318328..134318856,2	K562	blood:
5	chr2:134277466..134278009-chr2:134318355..134319063,2	MCF-7	breast:
6	chr2:134365245..134367451-chr2:134398214..134401016,3	MCF-7	breast:
7	chr2:134257170..134260161-chr2:134313651..134315459,2	MCF-7	breast:
8	chr2:134355111..134357281-chr2:134363291..134366211,2	K562	blood:
9	chr2:134383649..134385456-chr2:134399469..134401121,2	MCF-7	breast:
10	chr2:134355111..134357281-chr2:134363291..134366211,2	K562	blood:
11	chr2:134386454..134389246-chr2:134397997..134400619,2	MCF-7	breast:
12	chr2:134020255..134021142-chr2:134318343..134319277,2	MCF-7	breast:
13	chr2:134317582..134320224-chr2:134325327..134327285,2	K562	blood:
14	chr2:134178712..134179890-chr2:134318289..134319234,5	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MGAT5-1	chr2:134314323-134314418	ENSG00000223430
2	lnc-MGAT5-1	chr2:134311886-134312003	ENSG00000223430
3	lnc-MGAT5-5	chr2:134353662-134353970	NONHSAT074550
4	lnc-MGAT5-1	chr2:134315598-134315798	ENSG00000223430

Variant related genes	Relation type
ENSG00000223430	TF binding region
NCKAP5	TF binding region
RN7SKP93	TF binding region
ENSG00000223430	CpG island
NCKAP5	CpG island
RN7SKP93	CpG island
ENSG00000176771	chromatin interactions

Extended variants
information (count: 3362 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:3362 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11684547	chr2:134301130-134301131	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs11684591	chr2:134301195-134301196	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs554799999	chr2:134301262-134301263	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs77988939	chr2:134301354-134301355	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543211682	chr2:134301391-134301392	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558358949	chr2:134301428-134301429	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577702969	chr2:134301495-134301496	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35570016	chr2:134301544-134301545	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs183123216	chr2:134301590-134301591	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188068374	chr2:134301608-134301609	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141896186	chr2:134301622-134301623	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542663145	chr2:134301642-134301643	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs193064465	chr2:134301659-134301660	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142219586	chr2:134301662-134301663	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs151209722	chr2:134301669-134301670	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551667198	chr2:134301692-134301693	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571903982	chr2:134301693-134301694	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576793995	chr2:134301757-134301758	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532768915	chr2:134301770-134301771	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35399323	chr2:134301805-134301806	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185301533	chr2:134301815-134301816	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565639731	chr2:134301847-134301848	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536236639	chr2:134301859-134301860	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs57864833	chr2:134301919-134301920	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs58003178	chr2:134301929-134301930	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs189425102	chr2:134301949-134301950	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536984057	chr2:134301956-134301957	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs141344254	chr2:134301967-134301968	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs59418700	chr2:134301972-134301973	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs574987031	chr2:134301995-134301996	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142510156	chr2:134302020-134302021	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534513765	chr2:134302025-134302026	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554200722	chr2:134302034-134302035	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145202390	chr2:134302037-134302038	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543003681	chr2:134302054-134302055	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192695626	chr2:134302093-134302094	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs78541077	chr2:134302110-134302111	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34876294	chr2:134302135-134302136	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs565599665	chr2:134302136-134302137	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532704786	chr2:134302177-134302178	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369118346	chr2:134302204-134302205	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576035946	chr2:134302205-134302206	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547682443	chr2:134302208-134302209	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577412975	chr2:134302228-134302229	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184931410	chr2:134302238-134302239	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377299884	chr2:134302263-134302264	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188129550	chr2:134302277-134302278	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569515811	chr2:134302345-134302346	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147595248	chr2:134302362-134302363	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552008675	chr2:134302385-134302386	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	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	chr2:134286200-134311600	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr2:134290800-134324200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr2:134291200-134311400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:134292200-134304200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:134301000-134301400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr2:134301400-134302000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr2:134302800-134303800	Enhancers	Brain Substantia Nigra	brain
8	chr2:134303000-134303800	Enhancers	Brain Cingulate Gyrus	brain
9	chr2:134303800-134315800	Weak transcription	Brain Cingulate Gyrus	brain
10	chr2:134304000-134304400	Enhancers	H9 Cell Line	embryonic stem cell
11	chr2:134304000-134304800	Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr2:134304200-134304600	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr2:134304200-134305000	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr2:134304200-134305000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr2:134304200-134305000	Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr2:134304200-134305000	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr2:134304200-134310400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:134304400-134304600	Flanking Active TSS	H9 Cell Line	embryonic stem cell
19	chr2:134304400-134305000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr2:134304600-134305000	Active TSS	H9 Cell Line	embryonic stem cell
21	chr2:134304600-134305000	Active TSS	HUES64 Cell Line	embryonic stem cell
22	chr2:134304600-134305000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr2:134308800-134310800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr2:134310000-134313200	Weak transcription	Psoas Muscle	Psoas
25	chr2:134310400-134311200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr2:134310400-134311200	Enhancers	NHDF-Ad	bronchial
27	chr2:134310400-134312000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr2:134310400-134315000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr2:134310400-134324000	Weak transcription	NHEK	skin
30	chr2:134310800-134311200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr2:134310800-134311200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr2:134310800-134311200	Enhancers	Fetal Muscle Leg	muscle
33	chr2:134310800-134311600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr2:134310800-134313000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:134310800-134314800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr2:134311000-134315200	Weak transcription	Fetal Heart	heart
37	chr2:134311200-134312000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr2:134311200-134314800	Weak transcription	NHDF-Ad	bronchial
39	chr2:134311200-134323000	Weak transcription	Fetal Muscle Leg	muscle
40	chr2:134311400-134312600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr2:134311600-134314200	Strong transcription	Cortex derived primary cultured neurospheres	brain
42	chr2:134311600-134315200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr2:134311800-134312000	Enhancers	NH-A	brain
44	chr2:134312000-134314000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr2:134312000-134318400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr2:134312000-134323600	Weak transcription	NH-A	brain
47	chr2:134312600-134312800	Enhancers	Brain Substantia Nigra	brain
48	chr2:134312600-134321800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr2:134312800-134315200	Weak transcription	Brain Substantia Nigra	brain
50	chr2:134313000-134315200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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