Variant report

Variant	nsv875532
Chromosome Location	chr2:186309738-186422662
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:347)
CpG islands
(count:183)
Chromatin interactive
region (count:15)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:347 , 50 per page) page: 1 2 3 4 5 6 7

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	chr2:186414165-186414407	IMR90	lung:	n/a	chr2:186414287-186414298
7	CEBPB	chr2:186313713-186313937	HepG2	liver:	n/a	chr2:186313826-186313837 chr2:186313826-186313839
8	CEBPB	chr2:186328234-186328579	HepG2	liver:	n/a	chr2:186328405-186328416
9	CEBPB	chr2:186412355-186412597	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:186319765-186320025	HepG2	liver:	n/a	chr2:186319845-186319856 chr2:186319872-186319885 chr2:186319845-186319858
11	CEBPB	chr2:186389223-186389330	HepG2	liver:	n/a	chr2:186389247-186389258
12	CEBPB	chr2:186364789-186365076	HepG2	liver:	n/a	chr2:186364927-186364940 chr2:186364928-186364939 chr2:186364879-186364891
13	CEBPB	chr2:186414221-186414307	H1-hESC	embryonic stem cell:	n/a	chr2:186414287-186414298
14	CEBPB	chr2:186321229-186321715	HCT-116	colon:	n/a	n/a
15	CEBPB	chr2:186355813-186356061	HepG2	liver:	n/a	chr2:186355919-186355932 chr2:186355919-186355930
16	CEBPB	chr2:186326049-186326249	HepG2	liver:	n/a	chr2:186326152-186326163
17	CEBPB	chr2:186326140-186326258	A549	lung:	n/a	chr2:186326152-186326163
18	CEBPB	chr2:186328274-186328568	A549	lung:	n/a	chr2:186328405-186328416
19	CEBPB	chr2:186367300-186367396	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:186330125-186330406	HepG2	liver:	n/a	chr2:186330266-186330277
21	CEBPB	chr2:186414148-186414425	HepG2	liver:	n/a	chr2:186414287-186414298
22	CEBPB	chr2:186338338-186338358	HepG2	liver:	n/a	n/a
23	CHD2	chr2:186349402-186349696	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr2:186387320-186387470	HMEC	breast:	n/a	n/a
25	CTCF	chr2:186361280-186361430	GM12865	blood:	n/a	n/a
26	CTCF	chr2:186348660-186348757	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr2:186387331-186387451	HUVEC	blood vessel:	n/a	n/a
28	CTCF	chr2:186359746-186359802	GM20000	blood:	n/a	n/a
29	CTCF	chr2:186387338-186387488	GM13977	blood:	n/a	n/a
30	CTCF	chr2:186411871-186411904	Medullo	brain:	n/a	n/a
31	CTCF	chr2:186387300-186387450	RPTEC	kidney:	n/a	n/a
32	CTCF	chr2:186376959-186376991	K562	blood:	n/a	n/a
33	CTCF	chr2:186395980-186396130	GM12869	blood:	n/a	n/a
34	CTCF	chr2:186387260-186387410	HEK293	kidney:	n/a	n/a
35	CTCF	chr2:186387300-186387450	GM12873	blood:	n/a	n/a
36	CTCF	chr2:186387320-186387470	SAEC	small airway:	n/a	n/a
37	CTCF	chr2:186387260-186387410	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr2:186387229-186387553	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr2:186387351-186387423	K562	blood:	n/a	n/a
40	CTCF	chr2:186340780-186340930	HRE	kidney:	n/a	n/a
41	CTCF	chr2:186387280-186387430	Caco-2	colon:	n/a	n/a
42	CTCF	chr2:186340600-186340750	RPTEC	kidney:	n/a	n/a
43	CTCF	chr2:186387280-186387430	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr2:186340560-186340710	RPTEC	kidney:	n/a	n/a
45	CTCF	chr2:186387280-186387430	BE2_C	brain:	n/a	n/a
46	CTCF	chr2:186387268-186387458	HepG2	liver:	n/a	n/a
47	CTCF	chr2:186387360-186387510	HRE	kidney:	n/a	n/a
48	CTCF	chr2:186387200-186387350	A549	lung:	n/a	n/a
49	CTCF	chr2:186387280-186387430	HRE	kidney:	n/a	n/a
50	CTCF	chr2:186347614-186347651	NHEK	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:186412612-186412662	AoSMC	blood vessel:	n/a
2	chr2:186412073-186412123	PFSK-1	brain:	n/a
3	chr2:186412305-186412355	NH-A	brain:	n/a
4	chr2:186412073-186412123	U87	brain:	n/a
5	chr2:186412612-186412662	HIPEpiC	eye:	n/a
6	chr2:186412305-186412355	AG10803	skin:	n/a
7	chr2:186412305-186412355	Caco-2	colon:	n/a
8	chr2:186412073-186412123	HEEpiC	esophagus:	n/a
9	chr2:186412073-186412123	HEK293	kidney:	embryo
10	chr2:186412305-186412355	Hepatocyte	liver:	n/a
11	chr2:186412612-186412662	GM12878	blood:	n/a
12	chr2:186412073-186412123	ovcar-3	ovarian:	n/a
13	chr2:186412073-186412123	ProgFib	skin:	n/a
14	chr2:186412305-186412355	GM12878	blood:	n/a
15	chr2:186412612-186412662	HMEC	breast:	n/a
16	chr2:186412305-186412355	AG09319	gingival:	n/a
17	chr2:186412305-186412355	LNCaP	prostate:	n/a
18	chr2:186412612-186412662	HCPEpiC	choroid plexus:	n/a
19	chr2:186412073-186412123	AG04450	lung:	fetal
20	chr2:186412073-186412123	NB4	blood:	n/a
21	chr2:186412073-186412123	BE2_C	brain:	n/a
22	chr2:186412612-186412662	HAEpiC	amniotic membrane:	n/a
23	chr2:186412612-186412662	H1-hESC	embryonic stem cell:	embryo
24	chr2:186412612-186412662	T-47D	breast:	n/a
25	chr2:186412612-186412662	LNCaP	prostate:	n/a
26	chr2:186412305-186412355	BJ	skin:	n/a
27	chr2:186412073-186412123	BJ	skin:	n/a
28	chr2:186412305-186412355	AG04449	skin:	fetal
29	chr2:186412073-186412123	HUVEC	blood vessel:	n/a
30	chr2:186412612-186412662	GM19239	blood:	n/a
31	chr2:186412612-186412662	MCF-7	breast:	n/a
32	chr2:186412305-186412355	GM12892	blood:	n/a
33	chr2:186412305-186412355	HCF	heart:	n/a
34	chr2:186412612-186412662	Hela-S3	cervix:	n/a
35	chr2:186412305-186412355	K562	blood:	n/a
36	chr2:186412073-186412123	T-47D	breast:	n/a
37	chr2:186412305-186412355	H1-hESC	embryonic stem cell:	embryo
38	chr2:186412073-186412123	GM12891	blood:	n/a
39	chr2:186412612-186412662	AG04449	skin:	fetal
40	chr2:186412612-186412662	NB4	blood:	n/a
41	chr2:186412612-186412662	HRE	kidney:	n/a
42	chr2:186412305-186412355	IMR90	lung:	fetal
43	chr2:186412305-186412355	HepG2	liver:	n/a
44	chr2:186412073-186412123	HCPEpiC	choroid plexus:	n/a
45	chr2:186412305-186412355	U87	brain:	n/a
46	chr2:186412073-186412123	AG10803	skin:	n/a
47	chr2:186412305-186412355	HRCEpiC	kidney:	n/a
48	chr2:186412073-186412123	SKMC	muscle:	n/a
49	chr2:186412073-186412123	GM12878	blood:	n/a
50	chr2:186412073-186412123	NHDF-neo	bronchial:	n/a

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

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

(count:16 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 4138 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:4138 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10202955	chr2:186309738-186309739	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs558878372	chr2:186309922-186309923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77139040	chr2:186309926-186309927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535236187	chr2:186309936-186309937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373554641	chr2:186309944-186309945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201662780	chr2:186309994-186309995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145459896	chr2:186309997-186309998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34021136	chr2:186310000-186310001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368500880	chr2:186310050-186310051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138067684	chr2:186310052-186310053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182790235	chr2:186310098-186310099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs114860843	chr2:186310103-186310104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112067421	chr2:186310121-186310122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548243002	chr2:186310139-186310140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576587926	chr2:186310146-186310147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141892376	chr2:186310204-186310205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs80351194	chr2:186310248-186310249	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
18	rs530159967	chr2:186310317-186310318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542227961	chr2:186310350-186310351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560817520	chr2:186310374-186310375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150648912	chr2:186310415-186310416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12693410	chr2:186310420-186310421	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs550076885	chr2:186310479-186310480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139685497	chr2:186310511-186310512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535198137	chr2:186310528-186310529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188696757	chr2:186310554-186310555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564916646	chr2:186310557-186310558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527859912	chr2:186310558-186310559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565758969	chr2:186310563-186310564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190604705	chr2:186310576-186310577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183565999	chr2:186310578-186310579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552402896	chr2:186310591-186310592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187828145	chr2:186310604-186310605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs66554560	chr2:186310619-186310620	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs138869334	chr2:186310653-186310654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558779992	chr2:186310654-186310655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149354980	chr2:186310661-186310662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147529397	chr2:186310675-186310676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140194078	chr2:186310687-186310688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574584887	chr2:186310699-186310700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551851278	chr2:186310723-186310724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542359493	chr2:186310772-186310773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563635585	chr2:186310774-186310775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566978546	chr2:186310802-186310803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375319135	chr2:186310831-186310832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552305968	chr2:186310846-186310847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200941872	chr2:186310848-186310849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141248005	chr2:186310850-186310851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374038758	chr2:186310851-186310852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192401781	chr2:186310860-186310861	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:260 , 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	chr2:186309000-186314800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:186309400-186315000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr2:186312400-186315400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr2:186313600-186315800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:186314000-186315400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr2:186314000-186315800	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr2:186314400-186345200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr2:186314800-186316200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:186314800-186316400	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr2:186315000-186315400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
18	chr2:186315400-186315600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr2:186315400-186316400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr2:186315400-186317000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr2:186315600-186316200	Strong transcription	NHEK	skin
22	chr2:186315600-186318200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr2:186315800-186316200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:186315800-186316200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:186315800-186316400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr2:186315800-186316400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr2:186315800-186317000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
28	chr2:186316200-186317400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr2:186316200-186317600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr2:186316200-186318200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr2:186316200-186318400	Weak transcription	NHEK	skin
32	chr2:186316400-186317200	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr2:186316400-186317400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
34	chr2:186316400-186321600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr2:186316600-186319000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:186317000-186337400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr2:186317400-186318200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr2:186317400-186319000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr2:186317600-186317800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr2:186317800-186318400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:186318200-186318800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr2:186318400-186318600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:186318400-186318800	ZNF genes & repeats	NHEK	skin
44	chr2:186318800-186320200	Weak transcription	NHEK	skin
45	chr2:186318800-186320600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr2:186320200-186320600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
47	chr2:186320200-186321400	Enhancers	HMEC	breast
48	chr2:186320200-186321600	Enhancers	NHEK	skin
49	chr2:186320600-186321200	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr2:186320600-186321800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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