Variant report

Variant	nsv875529
Chromosome Location	chr2:186303530-186434458
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:384)
CpG islands
(count:184)
Chromatin interactive
region (count:15)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:384 , 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	BACH1	chr2:186340618-186340908	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr2:186404043-186404204	GM12878	blood:	n/a	chr2:186404092-186404101
3	BCL3	chr2:186338970-186339324	GM12878	blood:	n/a	n/a
4	CBX3	chr2:186321328-186321586	HCT-116	colon:	n/a	n/a
5	CCNT2	chr2:186421366-186421432	K562	blood:	n/a	n/a
6	CEBPB	chr2:186321229-186321715	HCT-116	colon:	n/a	n/a
7	CEBPB	chr2:186389223-186389330	HepG2	liver:	n/a	chr2:186389247-186389258
8	CEBPB	chr2:186414221-186414307	H1-hESC	embryonic stem cell:	n/a	chr2:186414287-186414298
9	CEBPB	chr2:186364789-186365076	HepG2	liver:	n/a	chr2:186364927-186364940 chr2:186364928-186364939 chr2:186364879-186364891
10	CEBPB	chr2:186414148-186414425	HepG2	liver:	n/a	chr2:186414287-186414298
11	CEBPB	chr2:186412355-186412597	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:186367300-186367396	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:186319765-186320025	HepG2	liver:	n/a	chr2:186319845-186319856 chr2:186319872-186319885 chr2:186319845-186319858
14	CEBPB	chr2:186326049-186326249	HepG2	liver:	n/a	chr2:186326152-186326163
15	CEBPB	chr2:186330125-186330406	HepG2	liver:	n/a	chr2:186330266-186330277
16	CEBPB	chr2:186328274-186328568	A549	lung:	n/a	chr2:186328405-186328416
17	CEBPB	chr2:186355813-186356061	HepG2	liver:	n/a	chr2:186355919-186355932 chr2:186355919-186355930
18	CEBPB	chr2:186326140-186326258	A549	lung:	n/a	chr2:186326152-186326163
19	CEBPB	chr2:186328234-186328579	HepG2	liver:	n/a	chr2:186328405-186328416
20	CEBPB	chr2:186414165-186414407	IMR90	lung:	n/a	chr2:186414287-186414298
21	CEBPB	chr2:186313713-186313937	HepG2	liver:	n/a	chr2:186313826-186313837 chr2:186313826-186313839
22	CEBPB	chr2:186425216-186425355	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr2:186338338-186338358	HepG2	liver:	n/a	n/a
24	CHD1	chr2:186432962-186433012	GM12878	blood:	n/a	n/a
25	CHD2	chr2:186349402-186349696	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr2:186387280-186387430	GM12872	blood:	n/a	n/a
27	CTCF	chr2:186387401-186387475	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr2:186387320-186387470	GM12864	blood:	n/a	n/a
29	CTCF	chr2:186340700-186340850	MCF-7	breast:	n/a	n/a
30	CTCF	chr2:186306300-186306450	HEK293	kidney:	n/a	chr2:186306416-186306424 chr2:186306417-186306425
31	CTCF	chr2:186387300-186387450	HCT-116	colon:	n/a	n/a
32	CTCF	chr2:186340680-186340830	HAc	cerebellar:	n/a	n/a
33	CTCF	chr2:186387280-186387430	BE2_C	brain:	n/a	n/a
34	CTCF	chr2:186387260-186387410	SAEC	small airway:	n/a	n/a
35	CTCF	chr2:186340720-186340870	HMEC	breast:	n/a	n/a
36	CTCF	chr2:186387300-186387450	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:186387380-186387530	GM12875	blood:	n/a	n/a
38	CTCF	chr2:186340600-186340750	RPTEC	kidney:	n/a	n/a
39	CTCF	chr2:186387187-186387605	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:186387348-186387483	HepG2	liver:	n/a	n/a
41	CTCF	chr2:186306760-186306910	MCF-7	breast:	n/a	n/a
42	CTCF	chr2:186321749-186321801	GM10248	blood:	n/a	n/a
43	CTCF	chr2:186387320-186387470	HMEC	breast:	n/a	n/a
44	CTCF	chr2:186411871-186411904	Medullo	brain:	n/a	n/a
45	CTCF	chr2:186387240-186387390	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr2:186306360-186306510	HCT-116	colon:	n/a	chr2:186306416-186306424 chr2:186306417-186306425
47	CTCF	chr2:186387300-186387450	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr2:186340780-186340930	HRE	kidney:	n/a	n/a
49	CTCF	chr2:186340620-186340770	HVMF	connective:	n/a	n/a
50	CTCF	chr2:186395980-186396130	GM12869	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:186412073-186412123	GM12891	blood:	n/a
2	chr2:186412073-186412123	GM12891	blood:	n/a
3	chr2:186412612-186412662	SAEC	small airway:	n/a
4	chr2:186412305-186412355	HNPCEpiC	eye:	n/a
5	chr2:186412305-186412355	HCT-116	colon:	n/a
6	chr2:186412305-186412355	HMEC	breast:	n/a
7	chr2:186412073-186412123	GM12892	blood:	n/a
8	chr2:186412305-186412355	SK-N-SH_RA	brain:	n/a
9	chr2:186412612-186412662	AoSMC	blood vessel:	n/a
10	chr2:186412305-186412355	H1-hESC	embryonic stem cell:	embryo
11	chr2:186412073-186412123	U87	brain:	n/a
12	chr2:186412073-186412123	HEEpiC	esophagus:	n/a
13	chr2:186412073-186412123	MCF-7	breast:	n/a
14	chr2:186412073-186412123	LNCaP	prostate:	n/a
15	chr2:186412612-186412662	NT2-D1	testis:	n/a
16	chr2:186412305-186412355	SK-N-SH	brain:	n/a
17	chr2:186412305-186412355	ovcar-3	ovarian:	n/a
18	chr2:186412305-186412355	HRE	kidney:	n/a
19	chr2:186412305-186412355	AG04449	skin:	fetal
20	chr2:186412073-186412123	Caco-2	colon:	n/a
21	chr2:186412612-186412662	Jurkat	blood:	n/a
22	chr2:186412073-186412123	SKMC	muscle:	n/a
23	chr2:186412612-186412662	HUVEC	blood vessel:	n/a
24	chr2:186412305-186412355	HIPEpiC	eye:	n/a
25	chr2:186412612-186412662	HCF	heart:	n/a
26	chr2:186412305-186412355	NHBE	bronchial:	n/a
27	chr2:186412612-186412662	GM06990	blood:	n/a
28	chr2:186412612-186412662	AG04449	skin:	fetal
29	chr2:186412305-186412355	GM06990	blood:	n/a
30	chr2:186412612-186412662	Hepatocyte	liver:	n/a
31	chr2:186412305-186412355	HepG2	liver:	n/a
32	chr2:186412073-186412123	GM19239	blood:	n/a
33	chr2:186412305-186412355	PrEC	prostate:	n/a
34	chr2:186412073-186412123	IMR90	lung:	fetal
35	chr2:186412305-186412355	AG09309	skin:	n/a
36	chr2:186412305-186412355	SK-N-MC	brain:	n/a
37	chr2:186412305-186412355	SAEC	small airway:	n/a
38	chr2:186412073-186412123	SK-N-SH_RA	brain:	n/a
39	chr2:186412612-186412662	HEEpiC	esophagus:	n/a
40	chr2:186412305-186412355	HRCEpiC	kidney:	n/a
41	chr2:186412612-186412662	NHDF-neo	bronchial:	n/a
42	chr2:186412073-186412123	AG09309	skin:	n/a
43	chr2:186412612-186412662	AG09309	skin:	n/a
44	chr2:186412612-186412662	HNPCEpiC	eye:	n/a
45	chr2:186412612-186412662	PANC-1	pancreas:	n/a
46	chr2:186412073-186412123	HUVEC	blood vessel:	n/a
47	chr2:186412073-186412123	HRCEpiC	kidney:	n/a
48	chr2:186412305-186412355	RPTEC	kidney:	n/a
49	chr2:186412612-186412662	IMR90	lung:	fetal
50	chr2:186412612-186412662	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
2	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
3	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
4	chr1:174445047..174445587-chr2:186343137..186343750,2	MCF-7	breast:
5	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
6	chr15:50184826..50185646-chr2:186340212..186341106,2	MCF-7	breast:
7	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
8	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
9	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
10	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
11	chr2:186334605..186336794-chr2:186340639..186343119,2	MCF-7	breast:
12	chr2:186387075..186388294-chr2:186603348..186604298,5	MCF-7	breast:
13	chr2:186334605..186336794-chr2:186340639..186343119,2	MCF-7	breast:
14	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
15	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSIP2-5	chr2:186386989-186387497	NONHSAT075962
2	lnc-FSIP2-5	chr2:186369727-186370202	NONHSAT075962
3	lnc-FSIP2-5	chr2:186410448-186410599	NONHSAT075962
4	lnc-FSIP2-5	chr2:186411316-186411619	NONHSAT075962
5	lnc-FSIP2-5	chr2:186366772-186369632	NONHSAT075963
6	lnc-FSIP2-5	chr2:186347761-186347818	NONHSAT075962
7	lnc-FSIP2-5	chr2:186327396-186327672	NONHSAT075962
8	lnc-FSIP2-5	chr2:186370427-186370468	NONHSAT075962
9	lnc-ZSWIM2-15	chr2:186309034-186309104	ucscGeneNc_uc002upi_2
10	lnc-FSIP2-5	chr2:186408484-186409210	NONHSAT075962
11	lnc-FSIP2-5	chr2:186370211-186370365	NONHSAT075962
12	lnc-FSIP2-5	chr2:186410628-186411001	NONHSAT075962
13	lnc-ZSWIM2-15	chr2:186311542-186311686	ucscGeneNc_uc002upi_2
14	lnc-FSIP2-5	chr2:186371629-186371957	NONHSAT075962
15	lnc-FSIP2-5	chr2:186411283-186411299	NONHSAT075962
16	lnc-FSIP2-5	chr2:186403858-186404073	NONHSAT075962
17	lnc-FSIP2-5	chr2:186369880-186375991	NONHSAT075963

No data

Variant related genes	Relation type
ENSG00000225406	TF binding region
ENSG00000225406	CpG island
ENSG00000226747	chromatin interactions
ENSG00000188738	chromatin interactions

Extended variants
information (count: 4757 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:4757 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs767037	chr2:186303530-186303531	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs767038	chr2:186303556-186303557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185675631	chr2:186303685-186303686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553275095	chr2:186303711-186303712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568709917	chr2:186303738-186303739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536059761	chr2:186303770-186303771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573228838	chr2:186303820-186303821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540620051	chr2:186303874-186303875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576221095	chr2:186303937-186303938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11892010	chr2:186303945-186303946	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs190580130	chr2:186303959-186303960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76379576	chr2:186303983-186303984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs73049111	chr2:186304012-186304013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201760648	chr2:186304018-186304019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527465642	chr2:186304025-186304026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2113531	chr2:186304128-186304129	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs35432464	chr2:186304145-186304146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192412776	chr2:186304185-186304186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2042507	chr2:186304200-186304201	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs144230680	chr2:186304201-186304202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2113530	chr2:186304202-186304203	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs547584543	chr2:186304205-186304206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552265338	chr2:186304234-186304235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183877800	chr2:186304264-186304265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371465978	chr2:186304290-186304291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564537936	chr2:186304298-186304299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35920523	chr2:186304307-186304308	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs34995507	chr2:186304317-186304318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188107513	chr2:186304325-186304326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377535064	chr2:186304377-186304378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546923698	chr2:186304443-186304444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181307574	chr2:186304487-186304488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536023297	chr2:186304558-186304559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551218416	chr2:186304568-186304569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571618931	chr2:186304577-186304578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185670410	chr2:186304583-186304584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537185310	chr2:186304598-186304599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558261161	chr2:186304641-186304642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556460491	chr2:186304646-186304647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569968641	chr2:186304663-186304664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576821967	chr2:186304690-186304691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34080347	chr2:186304703-186304704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534323134	chr2:186304713-186304714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552805822	chr2:186304729-186304730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566398623	chr2:186304731-186304732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574406215	chr2:186304915-186304916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567405103	chr2:186304921-186304922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541594595	chr2:186304932-186304933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563170330	chr2:186304946-186304947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77477595	chr2:186305011-186305012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
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
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Autism	22543975	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186298200-186315800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:186298600-186315800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:186298800-186314800	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr2:186301800-186316600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:186302000-186320200	Weak transcription	HMEC	breast
6	chr2:186303000-186315600	Weak transcription	NHEK	skin
7	chr2:186303200-186318200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:186308400-186309000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:186309000-186314800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:186309400-186315000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr2:186312400-186315400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr2:186313600-186315800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:186314000-186315400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr2:186314000-186315800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr2:186314400-186345200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr2:186314800-186316200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr2:186314800-186316400	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr2:186315000-186315400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
19	chr2:186315400-186315600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr2:186315400-186316400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr2:186315400-186317000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr2:186315600-186316200	Strong transcription	NHEK	skin
23	chr2:186315600-186318200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr2:186315800-186316200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:186315800-186316200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:186315800-186316400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr2:186315800-186316400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr2:186315800-186317000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
29	chr2:186316200-186317400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr2:186316200-186317600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr2:186316200-186318200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr2:186316200-186318400	Weak transcription	NHEK	skin
33	chr2:186316400-186317200	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr2:186316400-186317400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
35	chr2:186316400-186321600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr2:186316600-186319000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:186317000-186337400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr2:186317400-186318200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr2:186317400-186319000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr2:186317600-186317800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:186317800-186318400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:186318200-186318800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr2:186318400-186318600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:186318400-186318800	ZNF genes & repeats	NHEK	skin
45	chr2:186318800-186320200	Weak transcription	NHEK	skin
46	chr2:186318800-186320600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr2:186320200-186320600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
48	chr2:186320200-186321400	Enhancers	HMEC	breast
49	chr2:186320200-186321600	Enhancers	NHEK	skin
50	chr2:186320600-186321200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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