Variant report

Variant	nsv875543
Chromosome Location	chr2:186365918-186489537
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:503)
CpG islands
(count:245)
Chromatin interactive
region (count:9)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:503 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	CBX3	chr2:186447908-186448538	HCT-116	colon:	n/a	n/a
3	CBX3	chr2:186447981-186448661	HCT-116	colon:	n/a	n/a
4	CCNT2	chr2:186421366-186421432	K562	blood:	n/a	n/a
5	CEBPB	chr2:186478710-186478888	A549	lung:	n/a	chr2:186478732-186478743
6	CEBPB	chr2:186448052-186448719	HCT-116	colon:	n/a	n/a
7	CEBPB	chr2:186412355-186412597	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:186389223-186389330	HepG2	liver:	n/a	chr2:186389247-186389258
9	CEBPB	chr2:186448144-186448607	MCF-7	breast:	n/a	n/a
10	CEBPB	chr2:186448129-186448586	A549	lung:	n/a	n/a
11	CEBPB	chr2:186448119-186448613	MCF-7	breast:	n/a	n/a
12	CEBPB	chr2:186367300-186367396	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:186425216-186425355	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr2:186448257-186448516	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:186448143-186448675	HCT-116	colon:	n/a	n/a
16	CEBPB	chr2:186414148-186414425	HepG2	liver:	n/a	chr2:186414287-186414298
17	CEBPB	chr2:186448257-186448571	A549	lung:	n/a	n/a
18	CEBPB	chr2:186447957-186448588	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:186478620-186478884	HepG2	liver:	n/a	chr2:186478732-186478743
20	CEBPB	chr2:186465657-186465842	A549	lung:	n/a	n/a
21	CEBPB	chr2:186414165-186414407	IMR90	lung:	n/a	chr2:186414287-186414298
22	CEBPB	chr2:186414221-186414307	H1-hESC	embryonic stem cell:	n/a	chr2:186414287-186414298
23	CHD1	chr2:186432962-186433012	GM12878	blood:	n/a	n/a
24	CHD2	chr2:186448192-186448572	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr2:186387260-186387410	GM12865	blood:	n/a	n/a
26	CTCF	chr2:186473720-186473870	AG04450	lung:	n/a	n/a
27	CTCF	chr2:186473620-186473770	NHEK	skin:	n/a	chr2:186473696-186473704
28	CTCF	chr2:186387360-186387510	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr2:186387348-186387483	HepG2	liver:	n/a	n/a
30	CTCF	chr2:186387300-186387450	GM12873	blood:	n/a	n/a
31	CTCF	chr2:186473443-186473985	A549	lung:	n/a	chr2:186473696-186473704
32	CTCF	chr2:186387260-186387410	SAEC	small airway:	n/a	n/a
33	CTCF	chr2:186387360-186387510	HRE	kidney:	n/a	n/a
34	CTCF	chr2:186473580-186473730	HMEC	breast:	n/a	chr2:186473696-186473704
35	CTCF	chr2:186473559-186473880	HepG2	liver:	n/a	chr2:186473696-186473704
36	CTCF	chr2:186473660-186473810	HMF	breast:	n/a	chr2:186473696-186473704
37	CTCF	chr2:186483634-186483696	MCF-7	breast:	n/a	n/a
38	CTCF	chr2:186483593-186483678	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:186478804-186478845	GM10248	blood:	n/a	n/a
40	CTCF	chr2:186387360-186387510	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr2:186473643-186473820	HUVEC	blood vessel:	n/a	chr2:186473696-186473704
42	CTCF	chr2:186473600-186473750	BE2_C	brain:	n/a	chr2:186473696-186473704
43	CTCF	chr2:186473640-186473790	BE2_C	brain:	n/a	chr2:186473696-186473704
44	CTCF	chr2:186455420-186455486	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr2:186483580-186483730	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr2:186416060-186416210	HepG2	liver:	n/a	n/a
47	CTCF	chr2:186387351-186387423	K562	blood:	n/a	n/a
48	CTCF	chr2:186483620-186483770	SAEC	small airway:	n/a	n/a
49	CTCF	chr2:186387240-186387390	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr2:186473620-186473770	SK-N-SH_RA	brain:	n/a	chr2:186473696-186473704

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:186412073-186412123	Caco-2	colon:	n/a
2	chr2:186412073-186412123	Caco-2	colon:	n/a
3	chr2:186412305-186412355	SKMC	muscle:	n/a
4	chr2:186412073-186412123	NT2-D1	testis:	n/a
5	chr2:186412305-186412355	SAEC	small airway:	n/a
6	chr2:186412305-186412355	AG09319	gingival:	n/a
7	chr2:186412305-186412355	ProgFib	skin:	n/a
8	chr2:186412073-186412123	ECC-1	luminal epithelium:	n/a
9	chr2:186443903-186443953	GM12891	blood:	n/a
10	chr2:186443903-186443953	HRPEpiC	eye:	n/a
11	chr2:186412073-186412123	SKMC	muscle:	n/a
12	chr2:186412073-186412123	HRE	kidney:	n/a
13	chr2:186412305-186412355	A549	lung:	n/a
14	chr2:186443903-186443953	NHDF-neo	bronchial:	n/a
15	chr2:186412305-186412355	BJ	skin:	n/a
16	chr2:186412612-186412662	BJ	skin:	n/a
17	chr2:186412305-186412355	HRCEpiC	kidney:	n/a
18	chr2:186412612-186412662	NHBE	bronchial:	n/a
19	chr2:186443903-186443953	GM12892	blood:	n/a
20	chr2:186412305-186412355	SK-N-MC	brain:	n/a
21	chr2:186412612-186412662	PrEC	prostate:	n/a
22	chr2:186412612-186412662	RPTEC	kidney:	n/a
23	chr2:186412612-186412662	HRE	kidney:	n/a
24	chr2:186412305-186412355	HCT-116	colon:	n/a
25	chr2:186412612-186412662	PANC-1	pancreas:	n/a
26	chr2:186412073-186412123	HCM	heart:	n/a
27	chr2:186443903-186443953	Hela-S3	cervix:	n/a
28	chr2:186412073-186412123	HCPEpiC	choroid plexus:	n/a
29	chr2:186412305-186412355	HPAEpiC	pulmonary alveolar:	n/a
30	chr2:186443903-186443953	SK-N-SH_RA	brain:	n/a
31	chr2:186412305-186412355	PrEC	prostate:	n/a
32	chr2:186412612-186412662	GM12891	blood:	n/a
33	chr2:186412073-186412123	NB4	blood:	n/a
34	chr2:186412612-186412662	HRPEpiC	eye:	n/a
35	chr2:186412612-186412662	SK-N-MC	brain:	n/a
36	chr2:186412073-186412123	GM12878	blood:	n/a
37	chr2:186443903-186443953	GM12878	blood:	n/a
38	chr2:186412073-186412123	ovcar-3	ovarian:	n/a
39	chr2:186412073-186412123	PANC-1	pancreas:	n/a
40	chr2:186412305-186412355	Hepatocyte	liver:	n/a
41	chr2:186412073-186412123	BJ	skin:	n/a
42	chr2:186412612-186412662	MCF-7	breast:	n/a
43	chr2:186412612-186412662	AG10803	skin:	n/a
44	chr2:186412073-186412123	AoSMC	blood vessel:	n/a
45	chr2:186412305-186412355	Caco-2	colon:	n/a
46	chr2:186412305-186412355	HepG2	liver:	n/a
47	chr2:186412305-186412355	AG04449	skin:	fetal
48	chr2:186443903-186443953	Caco-2	colon:	n/a
49	chr2:186412612-186412662	ECC-1	luminal epithelium:	n/a
50	chr2:186412305-186412355	Jurkat	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:186387075..186388294-chr2:186603348..186604298,5	MCF-7	breast:
2	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
3	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
4	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
5	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
6	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
7	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
8	chr2:186473268..186473794-chr2:186603435..186603983,2	MCF-7	breast:
9	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 4487 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:4487 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11900568	chr2:186365918-186365919	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs548535462	chr2:186365919-186365920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79402379	chr2:186365932-186365933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs77980700	chr2:186365937-186365938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs76374177	chr2:186365941-186365942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570211363	chr2:186365947-186365948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78363797	chr2:186365977-186365978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181730826	chr2:186365980-186365981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs78588866	chr2:186365987-186365988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537567174	chr2:186366011-186366012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556189827	chr2:186366026-186366027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569022703	chr2:186366033-186366034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138122298	chr2:186366077-186366078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185126820	chr2:186366085-186366086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553341910	chr2:186366107-186366108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572041599	chr2:186366118-186366119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534720283	chr2:186366124-186366125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542883317	chr2:186366145-186366146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536439063	chr2:186366182-186366183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73049136	chr2:186366207-186366208	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs207462729	chr2:186366234-186366235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543559649	chr2:186366274-186366275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189429462	chr2:186366298-186366299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532650980	chr2:186366307-186366308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547854362	chr2:186366334-186366335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181463414	chr2:186366357-186366358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559768843	chr2:186366368-186366369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530447926	chr2:186366460-186366461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548836319	chr2:186366529-186366530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570171151	chr2:186366531-186366532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537604265	chr2:186366540-186366541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs13384417	chr2:186366568-186366569	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs571049887	chr2:186366595-186366596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34081911	chr2:186366668-186366669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559926191	chr2:186366728-186366729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200190839	chr2:186366741-186366742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538330639	chr2:186366743-186366744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs397986929	chr2:186366747-186366748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553378465	chr2:186366827-186366828	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs533818773	chr2:186366914-186366915	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs558444011	chr2:186366954-186366955	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs571677628	chr2:186366979-186366980	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs536167942	chr2:186367044-186367045	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs554805913	chr2:186367078-186367079	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs576163243	chr2:186367091-186367092	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs186430547	chr2:186367106-186367107	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs191034353	chr2:186367167-186367168	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs577450472	chr2:186367172-186367173	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs79110089	chr2:186367173-186367174	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs559809435	chr2:186367254-186367255	Weak transcription Strong transcription	lncRNA	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:171 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186342800-186368000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:186359200-186368200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:186359400-186367200	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr2:186359600-186368000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:186359800-186393400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr2:186361400-186368000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:186365800-186374600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr2:186367200-186368400	Strong transcription	HUES6 Cell Line	embryonic stem cell
9	chr2:186368000-186368600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr2:186368000-186369400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:186368200-186368600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
12	chr2:186368400-186368800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
13	chr2:186368600-186371400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr2:186368800-186372600	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr2:186369400-186372400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:186371400-186372400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr2:186372400-186372800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr2:186372400-186372800	ZNF genes & repeats	Pancreas	Pancrea
19	chr2:186372400-186373000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr2:186372400-186373000	ZNF genes & repeats	HMEC	breast
21	chr2:186372600-186373000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
22	chr2:186374200-186375400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr2:186374200-186376000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
24	chr2:186374200-186376000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr2:186374200-186376400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:186374200-186376400	ZNF genes & repeats	Adipose Nuclei	Adipose
27	chr2:186374600-186374800	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr2:186374600-186374800	ZNF genes & repeats	Psoas Muscle	Psoas
29	chr2:186375600-186376400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
30	chr2:186376400-186379200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr2:186376400-186382200	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr2:186378200-186381000	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr2:186379200-186379400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr2:186379400-186380600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr2:186380600-186381400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr2:186381200-186393800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr2:186381400-186432400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr2:186383200-186384000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr2:186383400-186383800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr2:186388000-186388200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr2:186388000-186388600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr2:186388200-186389600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr2:186393800-186394200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr2:186393800-186394600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr2:186394000-186394400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr2:186394000-186394600	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr2:186394400-186402200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr2:186396600-186396800	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr2:186396800-186398000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr2:186398000-186398600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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