Variant report

Variant	esv3405372
Chromosome Location	chr4:16226679-16229727
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:448)
CpG islands
(count:428)
Chromatin interactive
region (count:7)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:16226793-16227076	K562	blood:	n/a	n/a
2	ATF1	chr4:16228090-16228399	K562	blood:	n/a	chr4:16228224-16228238
3	ATF2	chr4:16226676-16227202	GM12878	blood:	n/a	n/a
4	ATF3	chr4:16228128-16228317	HepG2	liver:	n/a	chr4:16228228-16228238
5	ATF3	chr4:16228068-16228394	K562	blood:	n/a	chr4:16228228-16228238
6	BHLHE40	chr4:16227421-16227688	K562	blood:	n/a	n/a
7	BHLHE40	chr4:16228156-16228409	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:16227317-16227722	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:16227939-16228356	K562	blood:	n/a	n/a
10	BHLHE40	chr4:16228815-16228945	K562	blood:	n/a	chr4:16228815-16228831
11	BRCA1	chr4:16228685-16228864	Hela-S3	cervix:	n/a	n/a
12	CCNT2	chr4:16227278-16229113	K562	blood:	n/a	chr4:16227795-16227804 chr4:16228813-16228822 chr4:16228154-16228163
13	CEBPB	chr4:16228680-16228981	Hela-S3	cervix:	n/a	chr4:16228866-16228878
14	CEBPB	chr4:16227469-16228056	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:16226750-16227074	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:16226766-16227087	K562	blood:	n/a	n/a
17	CEBPB	chr4:16226759-16227141	Hela-S3	cervix:	n/a	n/a
18	CEBPD	chr4:16228183-16228571	HepG2	liver:	n/a	n/a
19	CHD1	chr4:16226879-16227693	GM12878	blood:	n/a	n/a
20	CHD1	chr4:16229420-16229538	GM12878	blood:	n/a	n/a
21	CHD1	chr4:16227900-16229043	GM12878	blood:	n/a	chr4:16228147-16228157 chr4:16228152-16228162
22	CHD1	chr4:16228876-16228963	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr4:16228347-16228624	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr4:16228679-16228806	GM12878	blood:	n/a	n/a
25	CHD2	chr4:16227751-16227906	GM12878	blood:	n/a	n/a
26	CHD2	chr4:16228838-16229221	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr4:16228211-16228411	GM12878	blood:	n/a	n/a
28	CHD2	chr4:16227493-16227564	K562	blood:	n/a	n/a
29	CHD2	chr4:16228217-16228364	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr4:16228735-16228752	K562	blood:	n/a	n/a
31	CREB1	chr4:16228015-16228541	A549	lung:	n/a	n/a
32	CREB1	chr4:16227972-16228511	K562	blood:	n/a	n/a
33	CREB1	chr4:16228140-16228339	ECC-1	luminal epithelium:	n/a	n/a
34	CREB1	chr4:16227956-16228467	HepG2	liver:	n/a	n/a
35	CREB1	chr4:16228147-16228410	A549	lung:	n/a	n/a
36	CREB1	chr4:16227976-16228470	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr4:16227828-16228594	HepG2	liver:	n/a	n/a
38	CREB1	chr4:16227983-16228525	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr4:16228026-16228388	ECC-1	luminal epithelium:	n/a	n/a
40	CREB1	chr4:16227973-16228511	GM12878	blood:	n/a	n/a
41	CREB1	chr4:16227920-16228543	K562	blood:	n/a	n/a
42	CREB1	chr4:16227904-16228545	GM12878	blood:	n/a	n/a
43	CTCF	chr4:16226880-16227030	HMF	breast:	n/a	n/a
44	CTCF	chr4:16226920-16227070	AG09319	gingival:	n/a	n/a
45	CTCF	chr4:16226880-16227030	HPF	lung:	n/a	n/a
46	CTCF	chr4:16226904-16227500	K562	blood:	n/a	chr4:16227285-16227293
47	CTCF	chr4:16226760-16226910	AG04450	lung:	n/a	n/a
48	CTCF	chr4:16226920-16227070	BJ	skin:	n/a	n/a
49	CTCF	chr4:16226880-16227030	AG10803	skin:	n/a	n/a
50	CTCF	chr4:16226840-16226990	HPAF	blood vessel:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:16228633-16228683	BE2_C	brain:	n/a
2	chr4:16228633-16228683	BE2_C	brain:	n/a
3	chr4:16228633-16228683	NHBE	bronchial:	n/a
4	chr4:16228062-16228112	NH-A	brain:	n/a
5	chr4:16227813-16227863	HAEpiC	amniotic membrane:	n/a
6	chr4:16227539-16227589	MCF10A-Er-Src	breast:	n/a
7	chr4:16229123-16229173	GM12892	blood:	n/a
8	chr4:16227539-16227589	AoSMC	blood vessel:	n/a
9	chr4:16228062-16228112	SAEC	small airway:	n/a
10	chr4:16229123-16229173	Hepatocyte	liver:	n/a
11	chr4:16228647-16228697	SAEC	small airway:	n/a
12	chr4:16228633-16228683	HepG2	liver:	n/a
13	chr4:16228647-16228697	HMEC	breast:	n/a
14	chr4:16228062-16228112	ProgFib	skin:	n/a
15	chr4:16228633-16228683	HUVEC	blood vessel:	n/a
16	chr4:16228633-16228683	NH-A	brain:	n/a
17	chr4:16227539-16227589	ECC-1	luminal epithelium:	n/a
18	chr4:16229123-16229173	HMEC	breast:	n/a
19	chr4:16227813-16227863	HCF	heart:	n/a
20	chr4:16229123-16229173	NHDF-neo	bronchial:	n/a
21	chr4:16228062-16228112	CMK	blood:	n/a
22	chr4:16229123-16229173	PANC-1	pancreas:	n/a
23	chr4:16229123-16229173	Hela-S3	cervix:	n/a
24	chr4:16228647-16228697	ProgFib	skin:	n/a
25	chr4:16228885-16228935	AoSMC	blood vessel:	n/a
26	chr4:16228062-16228112	NB4	blood:	n/a
27	chr4:16228062-16228112	MCF-7	breast:	n/a
28	chr4:16229123-16229173	MCF-7	breast:	n/a
29	chr4:16227539-16227589	NH-A	brain:	n/a
30	chr4:16228885-16228935	GM12878	blood:	n/a
31	chr4:16229123-16229173	MCF10A-Er-Src	breast:	n/a
32	chr4:16229123-16229173	HUVEC	blood vessel:	n/a
33	chr4:16227813-16227863	HIPEpiC	eye:	n/a
34	chr4:16228633-16228683	T-47D	breast:	n/a
35	chr4:16228647-16228697	H1-hESC	embryonic stem cell:	embryo
36	chr4:16229123-16229173	HepG2	liver:	n/a
37	chr4:16229123-16229173	AG09309	skin:	n/a
38	chr4:16228885-16228935	SKMC	muscle:	n/a
39	chr4:16227539-16227589	Hela-S3	cervix:	n/a
40	chr4:16227539-16227589	HL-60	blood:	n/a
41	chr4:16227539-16227589	BJ	skin:	n/a
42	chr4:16228062-16228112	AG04450	lung:	fetal
43	chr4:16228633-16228683	HCM	heart:	n/a
44	chr4:16227539-16227589	SK-N-SH	brain:	n/a
45	chr4:16228633-16228683	HCPEpiC	choroid plexus:	n/a
46	chr4:16229123-16229173	HIPEpiC	eye:	n/a
47	chr4:16227539-16227589	AG09309	skin:	n/a
48	chr4:16228647-16228697	SKMC	muscle:	n/a
49	chr4:16227539-16227589	PFSK-1	brain:	n/a
50	chr4:16228062-16228112	HRE	kidney:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:15681714..15684664-chr4:16226494..16229781,3	K562	blood:
2	chr4:15002785..15006911-chr4:16226901..16230678,5	K562	blood:
3	chr4:16212529..16219737-chr4:16225844..16229602,8	MCF-7	breast:
4	chr17:59476916..59479068-chr4:16227271..16228837,2	MCF-7	breast:
5	chr4:16216932..16218804-chr4:16227245..16229857,2	MCF-7	breast:
6	chr21:33104183..33104701-chr4:16227636..16228281,2	Hela-S3	cervix:
7	chr4:16227890..16229761-chr4:17577650..17579806,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD38-2	chr4:16228286-16228800	NONHSAT095674
2	lnc-CD38-2	chr4:16228286-16230207	ENSG00000263327.2
3	lnc-CD38-2	chr4:16228630-16228800	ENSG00000263327.1
4	lnc-CD38-2	chr4:16228668-16228800	ENSG00000263327.1
5	lnc-CD38-2	chr4:16228308-16228800	ENSG00000263327.1
6	lnc-CD38-2	chr4:16228286-16228800	ENSG00000225917

No data

Variant related genes	Relation type
TAPT1-AS1	TF binding region
TAPT1	TF binding region
TAPT1-AS1	CpG island
TAPT1	CpG island
ENSG00000267280	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000156304	chromatin interactions
ENSG00000118564	chromatin interactions
ENSG00000137449	chromatin interactions
ENSG00000267131	chromatin interactions
ENSG00000002549	chromatin interactions
ENSG00000247624	chromatin interactions
ENSG00000237765	chromatin interactions
ENSG00000169762	chromatin interactions
PDGFRA	miRNA target sites

Extended variants
information (count: 94 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:94 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528514416	chr4:16226693-16226694	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs548359376	chr4:16226750-16226751	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs568564000	chr4:16226790-16226791	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs530677503	chr4:16226808-16226809	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs150672088	chr4:16226813-16226814	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs148643011	chr4:16226825-16226826	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs201012862	chr4:16226832-16226833	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs75179579	chr4:16226862-16226863	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs116239823	chr4:16226879-16226880	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs576588751	chr4:16226920-16226921	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs57495074	chr4:16226944-16226945	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs181934373	chr4:16227002-16227003	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs553261863	chr4:16227049-16227050	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs566331046	chr4:16227057-16227058	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs535444882	chr4:16227064-16227065	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs557559703	chr4:16227123-16227124	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs187574265	chr4:16227124-16227125	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs559226314	chr4:16227184-16227185	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs574994205	chr4:16227202-16227203	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs191456006	chr4:16227244-16227245	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs183601167	chr4:16227289-16227290	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs577068897	chr4:16227324-16227325	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs546156768	chr4:16227356-16227357	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs386672075	chr4:16227389-16227390	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs188491766	chr4:16227432-16227433	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs142041745	chr4:16227436-16227437	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs542211106	chr4:16227479-16227480	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs539874505	chr4:16227494-16227495	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs372445199	chr4:16227556-16227557	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs6812660	chr4:16227594-16227595	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs369738317	chr4:16227624-16227625	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs573445732	chr4:16227640-16227641	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
33	rs370126610	chr4:16227642-16227643	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs564253781	chr4:16227648-16227649	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs576219410	chr4:16227664-16227665	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs533189278	chr4:16227682-16227683	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs546542346	chr4:16227685-16227686	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs547336789	chr4:16227719-16227720	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs566779514	chr4:16227779-16227780	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs535058605	chr4:16227780-16227781	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs3749543	chr4:16227781-16227782	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs3749544	chr4:16227823-16227824	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs567614266	chr4:16227872-16227873	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs28384238	chr4:16227944-16227945	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
45	rs551534255	chr4:16228176-16228177	Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
46	rs557457554	chr4:16228189-16228190	Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
47	rs577006870	chr4:16228208-16228209	Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
48	rs12643453	chr4:16228250-16228251	Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
49	rs554214258	chr4:16228269-16228270	Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
50	rs553344607	chr4:16228315-16228316	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	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
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:418 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:16208800-16227200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:16214400-16226800	Weak transcription	Fetal Muscle Trunk	muscle
3	chr4:16224400-16227000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr4:16224400-16227000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:16224400-16227200	Enhancers	Small Intestine	intestine
6	chr4:16224600-16227000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr4:16224600-16227000	Flanking Active TSS	Liver	Liver
8	chr4:16224800-16227600	Flanking Active TSS	Primary hematopoietic stem cells	blood
9	chr4:16225000-16227200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
10	chr4:16225200-16227200	Flanking Active TSS	Primary T cells from cord blood	blood
11	chr4:16225600-16226800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:16225600-16226800	Flanking Active TSS	Brain Anterior Caudate	brain
13	chr4:16225600-16227000	Flanking Active TSS	Brain Substantia Nigra	brain
14	chr4:16225600-16227000	Flanking Active TSS	Hela-S3	cervix
15	chr4:16225600-16227200	Flanking Active TSS	Brain Angular Gyrus	brain
16	chr4:16225600-16227400	Flanking Active TSS	Primary B cells from cord blood	blood
17	chr4:16225600-16227600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
18	chr4:16225600-16230800	Active TSS	A549	lung
19	chr4:16225800-16226800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
20	chr4:16225800-16226800	Enhancers	HUVEC	blood vessel
21	chr4:16225800-16227000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr4:16225800-16227000	Flanking Active TSS	Fetal Brain Female	brain
23	chr4:16225800-16227000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
24	chr4:16225800-16227000	Flanking Active TSS	Rectal Smooth Muscle	rectum
25	chr4:16225800-16227200	Flanking Active TSS	Adipose Nuclei	Adipose
26	chr4:16225800-16227400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
27	chr4:16225800-16227400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
28	chr4:16225800-16227400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
29	chr4:16225800-16227400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr4:16225800-16227600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
31	chr4:16225800-16230000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr4:16226000-16226800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr4:16226000-16226800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr4:16226000-16226800	Flanking Active TSS	Fetal Lung	lung
35	chr4:16226000-16227000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:16226000-16227000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
37	chr4:16226000-16227000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr4:16226000-16227000	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
39	chr4:16226000-16227000	Flanking Active TSS	Fetal Kidney	kidney
40	chr4:16226000-16227400	Flanking Active TSS	Brain Germinal Matrix	brain
41	chr4:16226000-16227600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr4:16226200-16226800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
43	chr4:16226200-16226800	Enhancers	HSMMtube	muscle
44	chr4:16226200-16226800	Flanking Active TSS	NHLF	lung
45	chr4:16226200-16227000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr4:16226200-16227000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr4:16226200-16227200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr4:16226200-16227200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr4:16226200-16227200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr4:16226200-16227200	Flanking Active TSS	Fetal Heart	heart

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