Variant report

Variant	esv3403917
Chromosome Location	chr4:26861379-26864227
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:751)
CpG islands
(count:793)
Chromatin interactive
region (count:3)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:751 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:26863214-26863538	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:26861560-26862531	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:26861850-26862307	K562	blood:	n/a	n/a
4	ARID3A	chr4:26864099-26864296	HepG2	liver:	n/a	n/a
5	ATF1	chr4:26861911-26862326	K562	blood:	n/a	n/a
6	ATF2	chr4:26861949-26862304	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:26861869-26862290	GM12878	blood:	n/a	n/a
8	ATF2	chr4:26861733-26862562	GM12878	blood:	n/a	n/a
9	ATF2	chr4:26861882-26862245	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr4:26862942-26863703	GM12878	blood:	n/a	n/a
11	BACH1	chr4:26863641-26863760	K562	blood:	n/a	n/a
12	BACH1	chr4:26861654-26862335	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr4:26861980-26862222	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:26863290-26863677	GM12878	blood:	n/a	n/a
15	BCLAF1	chr4:26861860-26862543	GM12878	blood:	n/a	n/a
16	BCLAF1	chr4:26862989-26863832	GM12878	blood:	n/a	n/a
17	BCLAF1	chr4:26861869-26863686	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:26861691-26862490	HepG2	liver:	n/a	n/a
19	BHLHE40	chr4:26861771-26862522	K562	blood:	n/a	n/a
20	BHLHE40	chr4:26861695-26862548	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:26863044-26863310	K562	blood:	n/a	n/a
22	BHLHE40	chr4:26862882-26863688	GM12878	blood:	n/a	n/a
23	BRCA1	chr4:26861914-26862413	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr4:26862001-26862470	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr4:26861905-26862353	HepG2	liver:	n/a	n/a
26	CBX3	chr4:26861687-26862574	K562	blood:	n/a	n/a
27	CCNT2	chr4:26861919-26863302	K562	blood:	n/a	n/a
28	CEBPB	chr4:26861816-26862187	IMR90	lung:	n/a	n/a
29	CEBPB	chr4:26861833-26862170	A549	lung:	n/a	n/a
30	CEBPB	chr4:26861703-26862351	GM12878	blood:	n/a	n/a
31	CEBPB	chr4:26861810-26862541	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr4:26861800-26862120	HepG2	liver:	n/a	n/a
33	CEBPD	chr4:26861914-26862575	HepG2	liver:	n/a	n/a
34	CEBPD	chr4:26861902-26862397	K562	blood:	n/a	n/a
35	CEBPD	chr4:26861939-26862311	HepG2	liver:	n/a	n/a
36	CEBPZ	chr4:26861889-26862047	HepG2	liver:	n/a	n/a
37	CHD1	chr4:26861257-26864940	IMR90	lung:	n/a	n/a
38	CHD1	chr4:26861773-26862237	GM12878	blood:	n/a	n/a
39	CHD1	chr4:26862409-26863159	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr4:26863233-26863318	GM12878	blood:	n/a	n/a
41	CHD1	chr4:26862437-26862879	GM12878	blood:	n/a	n/a
42	CHD2	chr4:26861987-26862320	HepG2	liver:	n/a	n/a
43	CHD2	chr4:26862725-26862895	HepG2	liver:	n/a	n/a
44	CHD2	chr4:26862892-26862927	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr4:26862637-26862764	K562	blood:	n/a	n/a
46	CHD2	chr4:26861968-26862651	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr4:26861726-26862427	K562	blood:	n/a	n/a
48	CHD2	chr4:26861646-26862608	GM12878	blood:	n/a	n/a
49	CHD2	chr4:26863079-26863618	GM12878	blood:	n/a	n/a
50	CHD2	chr4:26861902-26862469	H1-hESC	embryonic stem cell:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:26862456-26862506	ECC-1	luminal epithelium:	n/a
2	chr4:26862182-26862232	PANC-1	pancreas:	n/a
3	chr4:26862852-26862902	AG04449	skin:	fetal
4	chr4:26863372-26863422	GM06990	blood:	n/a
5	chr4:26862197-26862247	HUVEC	blood vessel:	n/a
6	chr4:26862189-26862239	Hela-S3	cervix:	n/a
7	chr4:26862605-26862655	A549	lung:	n/a
8	chr4:26863372-26863422	NHBE	bronchial:	n/a
9	chr4:26862182-26862232	Jurkat	blood:	n/a
10	chr4:26862057-26862107	ProgFib	skin:	n/a
11	chr4:26862197-26862247	HRCEpiC	kidney:	n/a
12	chr4:26862852-26862902	GM12891	blood:	n/a
13	chr4:26863372-26863422	HRPEpiC	eye:	n/a
14	chr4:26863372-26863422	HepG2	liver:	n/a
15	chr4:26862182-26862232	H1-hESC	embryonic stem cell:	embryo
16	chr4:26862456-26862506	HCM	heart:	n/a
17	chr4:26862456-26862506	AG09309	skin:	n/a
18	chr4:26863112-26863162	HEK293	kidney:	embryo
19	chr4:26862182-26862232	GM12891	blood:	n/a
20	chr4:26862456-26862506	Hela-S3	cervix:	n/a
21	chr4:26862483-26862533	AG09309	skin:	n/a
22	chr4:26861983-26862033	GM19239	blood:	n/a
23	chr4:26862197-26862247	RPTEC	kidney:	n/a
24	chr4:26863372-26863422	HRE	kidney:	n/a
25	chr4:26861983-26862033	CMK	blood:	n/a
26	chr4:26862044-26862094	NH-A	brain:	n/a
27	chr4:26863237-26863287	AG04450	lung:	fetal
28	chr4:26862189-26862239	A549	lung:	n/a
29	chr4:26862483-26862533	NHDF-neo	bronchial:	n/a
30	chr4:26863372-26863422	BJ	skin:	n/a
31	chr4:26863237-26863287	T-47D	breast:	n/a
32	chr4:26863112-26863162	AG04450	lung:	fetal
33	chr4:26861983-26862033	HPAEpiC	pulmonary alveolar:	n/a
34	chr4:26862189-26862239	GM19239	blood:	n/a
35	chr4:26862189-26862239	HCPEpiC	choroid plexus:	n/a
36	chr4:26863372-26863422	AG04449	skin:	fetal
37	chr4:26862852-26862902	BJ	skin:	n/a
38	chr4:26862182-26862232	AG09319	gingival:	n/a
39	chr4:26862044-26862094	Jurkat	blood:	n/a
40	chr4:26863372-26863422	HCM	heart:	n/a
41	chr4:26863112-26863162	PrEC	prostate:	n/a
42	chr4:26861983-26862033	RPTEC	kidney:	n/a
43	chr4:26863372-26863422	AG09309	skin:	n/a
44	chr4:26862456-26862506	PrEC	prostate:	n/a
45	chr4:26862483-26862533	SKMC	muscle:	n/a
46	chr4:26862197-26862247	SK-N-SH_RA	brain:	n/a
47	chr4:26863372-26863422	SK-N-MC	brain:	n/a
48	chr4:26862852-26862902	K562	blood:	n/a
49	chr4:26862057-26862107	HL-60	blood:	n/a
50	chr4:26862197-26862247	ECC-1	luminal epithelium:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:42054703..42055601-chr4:26863001..26863501,2	NB4	blood:
2	chr4:26863995..26865710-chr4:27013310..27015079,2	K562	blood:
3	chr4:26863853..26865538-chr4:26880691..26883360,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCKAR-1	chr4:26861428-26861650	XLOC_003912
2	lnc-CCKAR-1	chr4:26861963-26862221	XLOC_003912
3	lnc-CCKAR-1	chr4:26861428-26861650	XLOC_003912
4	lnc-CCKAR-1	chr4:26862132-26862203	XLOC_003912
5	lnc-CCKAR-1	chr4:26861238-26861650	NONHSAT095890
6	lnc-CCKAR-1	chr4:26861437-26861650	XLOC_003912
7	lnc-CCKAR-1	chr4:26861963-26862284	NONHSAT095891
8	lnc-CCKAR-1	chr4:26862132-26862263	NONHSAT095890
9	lnc-CCKAR-1	chr4:26862223-26862250	XLOC_003912
10	lnc-CCKAR-1	chr4:26861319-26861650	NONHSAT095891

No data

Variant related genes	Relation type
STIM2	TF binding region
ENSG00000240005	TF binding region
STIM2	CpG island
ENSG00000240005	CpG island
ENSG00000182606	chromatin interactions
NFATC2IP	miRNA target sites
NFATC3	miRNA target sites

Extended variants
information (count: 114 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:114 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552857389	chr4:26861429-26861430	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs568863139	chr4:26861455-26861456	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs376380445	chr4:26861516-26861517	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs555343234	chr4:26861580-26861581	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs568780698	chr4:26861581-26861582	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs534345485	chr4:26861585-26861586	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs573806113	chr4:26861615-26861616	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs554430353	chr4:26861619-26861620	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs565507218	chr4:26861639-26861640	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs9790789	chr4:26861656-26861657	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs10029816	chr4:26861674-26861675	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs73116643	chr4:26861753-26861754	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs181280072	chr4:26861755-26861756	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs76558049	chr4:26861756-26861757	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs536794473	chr4:26861770-26861771	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs540009025	chr4:26861798-26861799	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs560310546	chr4:26861834-26861835	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs147487261	chr4:26861910-26861911	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs150327476	chr4:26861927-26861928	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs552295644	chr4:26861965-26861966	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs568752983	chr4:26861968-26861969	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs531293558	chr4:26862024-26862025	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs185049180	chr4:26862033-26862034	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs79065968	chr4:26862042-26862043	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs556723379	chr4:26862074-26862075	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs568743954	chr4:26862099-26862100	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs565589987	chr4:26862103-26862104	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs115332646	chr4:26862117-26862118	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs56169951	chr4:26862126-26862127	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs539544928	chr4:26862128-26862129	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs556656359	chr4:26862156-26862157	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs114834340	chr4:26862176-26862177	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs376620119	chr4:26862212-26862213	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs541773529	chr4:26862214-26862215	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs370744032	chr4:26862215-26862216	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs555362292	chr4:26862240-26862241	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs574355803	chr4:26862248-26862249	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs115262964	chr4:26862254-26862255	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs560087915	chr4:26862282-26862283	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs545743290	chr4:26862284-26862285	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs532377518	chr4:26862328-26862329	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs142821688	chr4:26862407-26862408	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs572301307	chr4:26862417-26862418	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs189561114	chr4:26862445-26862446	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs531458031	chr4:26862463-26862464	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
46	rs541430741	chr4:26862509-26862510	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
47	rs548175394	chr4:26862541-26862542	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs568099314	chr4:26862543-26862544	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs569988715	chr4:26862547-26862548	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs529396311	chr4:26862563-26862564	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Cancer	22183965	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD

Chromatin state (count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:26858600-26862800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:26858800-26861400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr4:26859400-26862200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr4:26859600-26861400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr4:26859600-26861800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
6	chr4:26859600-26861800	Flanking Active TSS	Duodenum Mucosa	Duodenum
7	chr4:26859600-26861800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
8	chr4:26859600-26862000	Flanking Active TSS	Fetal Thymus	thymus
9	chr4:26859800-26861800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr4:26859800-26861800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
11	chr4:26859800-26861800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
12	chr4:26859800-26861800	Enhancers	Spleen	Spleen
13	chr4:26859800-26862000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr4:26859800-26862000	Flanking Active TSS	Primary T cells from cord blood	blood
15	chr4:26859800-26862000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
16	chr4:26859800-26862000	Flanking Active TSS	Dnd41	blood
17	chr4:26859800-26862000	Flanking Active TSS	Hela-S3	cervix
18	chr4:26860000-26861600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr4:26860000-26861600	Weak transcription	Aorta	Aorta
20	chr4:26860000-26861600	Enhancers	Placenta Amnion	Placenta Amnion
21	chr4:26860000-26861800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:26860000-26861800	Weak transcription	Ovary	ovary
23	chr4:26860200-26861400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:26860200-26861400	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr4:26860200-26861600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr4:26860200-26861600	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr4:26860200-26861600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr4:26860200-26861600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr4:26860200-26861600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
30	chr4:26860200-26861600	Enhancers	Fetal Heart	heart
31	chr4:26860200-26861600	Enhancers	Left Ventricle	heart
32	chr4:26860200-26861600	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr4:26860200-26861800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr4:26860200-26861800	Enhancers	Small Intestine	intestine
35	chr4:26860200-26861800	Flanking Active TSS	NHEK	skin
36	chr4:26860200-26864600	Active TSS	Fetal Muscle Trunk	muscle
37	chr4:26860400-26861400	Enhancers	H1 Cell Line	embryonic stem cell
38	chr4:26860400-26861400	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr4:26860400-26861400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr4:26860400-26861400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr4:26860400-26861400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr4:26860400-26861400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr4:26860400-26861400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr4:26860400-26861400	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr4:26860400-26861400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr4:26860400-26861400	Enhancers	Adipose Nuclei	Adipose
47	chr4:26860400-26861400	Enhancers	Brain Anterior Caudate	brain
48	chr4:26860400-26861400	Enhancers	Brain Germinal Matrix	brain
49	chr4:26860400-26861400	Weak transcription	Fetal Brain Male	brain
50	chr4:26860400-26861400	Weak transcription	Rectal Smooth Muscle	rectum

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