Variant report

Variant	nsv875542
Chromosome Location	chr2:186358877-186422662
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:193)
CpG islands
(count:184)
Chromatin interactive
region (count:11)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:193 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr2:186404043-186404204	GM12878	blood:	n/a	chr2:186404092-186404101
2	CCNT2	chr2:186421366-186421432	K562	blood:	n/a	n/a
3	CEBPB	chr2:186389223-186389330	HepG2	liver:	n/a	chr2:186389247-186389258
4	CEBPB	chr2:186414165-186414407	IMR90	lung:	n/a	chr2:186414287-186414298
5	CEBPB	chr2:186414221-186414307	H1-hESC	embryonic stem cell:	n/a	chr2:186414287-186414298
6	CEBPB	chr2:186414148-186414425	HepG2	liver:	n/a	chr2:186414287-186414298
7	CEBPB	chr2:186412355-186412597	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:186364789-186365076	HepG2	liver:	n/a	chr2:186364927-186364940 chr2:186364928-186364939 chr2:186364879-186364891
9	CEBPB	chr2:186367300-186367396	HepG2	liver:	n/a	n/a
10	CTCF	chr2:186387300-186387450	RPTEC	kidney:	n/a	n/a
11	CTCF	chr2:186376959-186376991	K562	blood:	n/a	n/a
12	CTCF	chr2:186416060-186416210	HepG2	liver:	n/a	n/a
13	CTCF	chr2:186387201-186387561	GM12878	blood:	n/a	n/a
14	CTCF	chr2:186387335-186387472	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr2:186387300-186387450	GM12866	blood:	n/a	n/a
16	CTCF	chr2:186387240-186387390	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr2:186387272-186387522	MCF-7	breast:	n/a	n/a
18	CTCF	chr2:186387400-186387550	HepG2	liver:	n/a	n/a
19	CTCF	chr2:186381425-186381497	Medullo	brain:	n/a	n/a
20	CTCF	chr2:186394220-186394370	HFF-Myc	foreskin:	n/a	n/a
21	CTCF	chr2:186387301-186387496	LNCaP	prostate:	n/a	n/a
22	CTCF	chr2:186394437-186394585	GM12878	blood:	n/a	n/a
23	CTCF	chr2:186387187-186387605	MCF-7	breast:	n/a	n/a
24	CTCF	chr2:186387300-186387450	GM12878	blood:	n/a	n/a
25	CTCF	chr2:186387260-186387410	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr2:186387260-186387410	HEK293	kidney:	n/a	n/a
27	CTCF	chr2:186387352-186387400	GM10266	blood:	n/a	n/a
28	CTCF	chr2:186387380-186387530	GM12875	blood:	n/a	n/a
29	CTCF	chr2:186387300-186387450	MCF-7	breast:	n/a	n/a
30	CTCF	chr2:186359746-186359802	GM20000	blood:	n/a	n/a
31	CTCF	chr2:186387244-186387623	MCF-7	breast:	n/a	n/a
32	CTCF	chr2:186387360-186387510	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr2:186387200-186387350	A549	lung:	n/a	n/a
34	CTCF	chr2:186387260-186387410	GM12865	blood:	n/a	n/a
35	CTCF	chr2:186395980-186396130	GM12869	blood:	n/a	n/a
36	CTCF	chr2:186411005-186411020	GM10248	blood:	n/a	n/a
37	CTCF	chr2:186387320-186387470	GM12864	blood:	n/a	n/a
38	CTCF	chr2:186387320-186387470	SAEC	small airway:	n/a	n/a
39	CTCF	chr2:186387360-186387510	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr2:186411871-186411904	Medullo	brain:	n/a	n/a
41	CTCF	chr2:186386980-186387130	HL-60	blood:	n/a	n/a
42	CTCF	chr2:186387308-186387447	GM12878	blood:	n/a	n/a
43	CTCF	chr2:186387360-186387510	HRE	kidney:	n/a	n/a
44	CTCF	chr2:186387320-186387470	GM12874	blood:	n/a	n/a
45	CTCF	chr2:186387348-186387483	HepG2	liver:	n/a	n/a
46	CTCF	chr2:186387260-186387410	HMF	breast:	n/a	n/a
47	CTCF	chr2:186387260-186387410	SAEC	small airway:	n/a	n/a
48	CTCF	chr2:186387320-186387470	HMEC	breast:	n/a	n/a
49	CTCF	chr2:186387260-186387410	GM12864	blood:	n/a	n/a
50	CTCF	chr2:186387280-186387430	BE2_C	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:186412612-186412662	AG09319	gingival:	n/a
2	chr2:186412612-186412662	AG09319	gingival:	n/a
3	chr2:186412612-186412662	U87	brain:	n/a
4	chr2:186412073-186412123	GM12892	blood:	n/a
5	chr2:186412612-186412662	HEK293	kidney:	embryo
6	chr2:186412305-186412355	CMK	blood:	n/a
7	chr2:186412073-186412123	Jurkat	blood:	n/a
8	chr2:186412305-186412355	HCF	heart:	n/a
9	chr2:186412305-186412355	SK-N-MC	brain:	n/a
10	chr2:186412073-186412123	AG04449	skin:	fetal
11	chr2:186412073-186412123	Caco-2	colon:	n/a
12	chr2:186412612-186412662	NHBE	bronchial:	n/a
13	chr2:186412073-186412123	PANC-1	pancreas:	n/a
14	chr2:186412612-186412662	AG09309	skin:	n/a
15	chr2:186412305-186412355	H1-hESC	embryonic stem cell:	embryo
16	chr2:186412073-186412123	HEEpiC	esophagus:	n/a
17	chr2:186412305-186412355	HMEC	breast:	n/a
18	chr2:186412305-186412355	PANC-1	pancreas:	n/a
19	chr2:186412612-186412662	HCPEpiC	choroid plexus:	n/a
20	chr2:186412073-186412123	HRPEpiC	eye:	n/a
21	chr2:186412073-186412123	HUVEC	blood vessel:	n/a
22	chr2:186412073-186412123	IMR90	lung:	fetal
23	chr2:186412073-186412123	HCT-116	colon:	n/a
24	chr2:186412073-186412123	LNCaP	prostate:	n/a
25	chr2:186412612-186412662	HEEpiC	esophagus:	n/a
26	chr2:186412612-186412662	T-47D	breast:	n/a
27	chr2:186412073-186412123	AG04450	lung:	fetal
28	chr2:186412612-186412662	SK-N-MC	brain:	n/a
29	chr2:186412612-186412662	HNPCEpiC	eye:	n/a
30	chr2:186412305-186412355	HepG2	liver:	n/a
31	chr2:186412305-186412355	HUVEC	blood vessel:	n/a
32	chr2:186412305-186412355	AG04449	skin:	fetal
33	chr2:186412305-186412355	A549	lung:	n/a
34	chr2:186412305-186412355	GM19239	blood:	n/a
35	chr2:186412612-186412662	LNCaP	prostate:	n/a
36	chr2:186412305-186412355	IMR90	lung:	fetal
37	chr2:186412073-186412123	AG09309	skin:	n/a
38	chr2:186412073-186412123	SAEC	small airway:	n/a
39	chr2:186412305-186412355	GM06990	blood:	n/a
40	chr2:186412305-186412355	ProgFib	skin:	n/a
41	chr2:186412305-186412355	SAEC	small airway:	n/a
42	chr2:186412612-186412662	NHDF-neo	bronchial:	n/a
43	chr2:186412305-186412355	K562	blood:	n/a
44	chr2:186412073-186412123	SK-N-MC	brain:	n/a
45	chr2:186412073-186412123	PFSK-1	brain:	n/a
46	chr2:186412612-186412662	HAEpiC	amniotic membrane:	n/a
47	chr2:186412305-186412355	HRE	kidney:	n/a
48	chr2:186412073-186412123	K562	blood:	n/a
49	chr2:186412073-186412123	NHDF-neo	bronchial:	n/a
50	chr2:186412305-186412355	RPTEC	kidney:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
2	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
3	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
4	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
5	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
6	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
7	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
8	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
9	chr2:186387075..186388294-chr2:186603348..186604298,5	MCF-7	breast:
10	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
11	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSIP2-5	chr2:186369727-186370202	NONHSAT075962
2	lnc-FSIP2-5	chr2:186370427-186370468	NONHSAT075962
3	lnc-FSIP2-5	chr2:186410628-186411001	NONHSAT075962
4	lnc-FSIP2-5	chr2:186369880-186375991	NONHSAT075963
5	lnc-FSIP2-5	chr2:186403858-186404073	NONHSAT075962
6	lnc-FSIP2-5	chr2:186411316-186411619	NONHSAT075962
7	lnc-FSIP2-5	chr2:186370211-186370365	NONHSAT075962
8	lnc-FSIP2-5	chr2:186366772-186369632	NONHSAT075963
9	lnc-FSIP2-5	chr2:186411283-186411299	NONHSAT075962
10	lnc-FSIP2-5	chr2:186410448-186410599	NONHSAT075962
11	lnc-FSIP2-5	chr2:186371629-186371957	NONHSAT075962
12	lnc-FSIP2-5	chr2:186408484-186409210	NONHSAT075962
13	lnc-FSIP2-5	chr2:186386989-186387497	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: 2330 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:2330 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35201815	chr2:186358877-186358878	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs183528857	chr2:186358902-186358903	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs573172636	chr2:186358979-186358980	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs571606920	chr2:186359001-186359002	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73982023	chr2:186359010-186359011	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs547511595	chr2:186359068-186359069	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566062627	chr2:186359184-186359185	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs114405035	chr2:186359190-186359191	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555273333	chr2:186359193-186359194	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144676923	chr2:186359199-186359200	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540317086	chr2:186359213-186359214	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537207289	chr2:186359228-186359229	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556226564	chr2:186359249-186359250	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577705861	chr2:186359251-186359252	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545072488	chr2:186359269-186359270	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369265545	chr2:186359277-186359278	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571681662	chr2:186359285-186359286	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11683123	chr2:186359287-186359288	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs376479935	chr2:186359293-186359294	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560811362	chr2:186359314-186359315	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531539638	chr2:186359324-186359325	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543296627	chr2:186359326-186359327	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565079107	chr2:186359329-186359330	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544303598	chr2:186359360-186359361	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369403606	chr2:186359404-186359405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532530461	chr2:186359409-186359410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188487053	chr2:186359435-186359436	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547845710	chr2:186359439-186359440	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148514709	chr2:186359458-186359459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530080761	chr2:186359501-186359502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548908809	chr2:186359588-186359589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs118132402	chr2:186359597-186359598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs13010482	chr2:186359617-186359618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs67784166	chr2:186359638-186359639	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs558921351	chr2:186359670-186359671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571003710	chr2:186359671-186359672	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538378360	chr2:186359677-186359678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553419399	chr2:186359680-186359681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557595421	chr2:186359693-186359694	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535801407	chr2:186359728-186359729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554143277	chr2:186359776-186359777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs114565445	chr2:186359824-186359825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370380107	chr2:186359841-186359842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374900032	chr2:186359916-186359917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs55733417	chr2:186360012-186360013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576939353	chr2:186360029-186360030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs397986928	chr2:186360030-186360031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs193110889	chr2:186360055-186360056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376055455	chr2:186360081-186360082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367907327	chr2:186360099-186360100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186342800-186368000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:186350000-186360600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr2:186350000-186360800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr2:186350400-186361000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr2:186358400-186359000	Strong transcription	H1 Cell Line	embryonic stem cell
6	chr2:186358400-186359200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr2:186358400-186359400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:186358400-186359400	Strong transcription	HUES6 Cell Line	embryonic stem cell
9	chr2:186358600-186359200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr2:186358600-186359400	Strong transcription	HMEC	breast
11	chr2:186358800-186359200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:186358800-186359600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr2:186358800-186359800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr2:186359000-186359200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
15	chr2:186359200-186360000	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr2:186359200-186360800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:186359200-186361000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr2:186359200-186361000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr2:186359200-186368200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr2:186359400-186361800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:186359400-186364800	Weak transcription	HMEC	breast
22	chr2:186359400-186367200	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr2:186359600-186368000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr2:186359800-186393400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:186360600-186360800	Enhancers	H9 Cell Line	embryonic stem cell
26	chr2:186361000-186361400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr2:186361400-186368000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr2:186365800-186374600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr2:186367200-186368400	Strong transcription	HUES6 Cell Line	embryonic stem cell
30	chr2:186368000-186368600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr2:186368000-186369400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr2:186368200-186368600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
33	chr2:186368400-186368800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
34	chr2:186368600-186371400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr2:186368800-186372600	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr2:186369400-186372400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:186371400-186372400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr2:186372400-186372800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr2:186372400-186372800	ZNF genes & repeats	Pancreas	Pancrea
40	chr2:186372400-186373000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr2:186372400-186373000	ZNF genes & repeats	HMEC	breast
42	chr2:186372600-186373000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
43	chr2:186374200-186375400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:186374200-186376000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
45	chr2:186374200-186376000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr2:186374200-186376400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr2:186374200-186376400	ZNF genes & repeats	Adipose Nuclei	Adipose
48	chr2:186374600-186374800	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr2:186374600-186374800	ZNF genes & repeats	Psoas Muscle	Psoas
50	chr2:186375600-186376400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell

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