Variant report

Variant	esv1817026
Chromosome Location	chr7:123885477-124039708
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:584)
CpG islands
(count:244)
Chromatin interactive
region (count:14)
LncRNA
region (count:33)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:123903518-123903832	K562	blood:	n/a	n/a
2	ATF1	chr7:124026607-124026805	K562	blood:	n/a	n/a
3	ATF1	chr7:123953326-123953442	K562	blood:	n/a	n/a
4	ATF1	chr7:123886598-123886729	K562	blood:	n/a	n/a
5	ATF1	chr7:123909888-123910120	K562	blood:	n/a	n/a
6	ATF1	chr7:123950919-123951365	K562	blood:	n/a	n/a
7	ATF2	chr7:123897573-123898594	GM12878	blood:	n/a	n/a
8	ATF2	chr7:123903345-123903808	GM12878	blood:	n/a	n/a
9	ATF3	chr7:123903479-123903869	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr7:123903532-123903773	GM12878	blood:	n/a	n/a
11	ATF3	chr7:123903568-123903806	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:124009494-124009604	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr7:123897707-123898119	GM12878	blood:	n/a	chr7:123897898-123897908 chr7:123897902-123897912 chr7:123897901-123897912
14	BATF	chr7:123903522-123903804	GM12878	blood:	n/a	n/a
15	BATF	chr7:123903526-123903804	GM12878	blood:	n/a	n/a
16	BATF	chr7:123885688-123885883	GM12878	blood:	n/a	chr7:123885771-123885782
17	BATF	chr7:123885644-123885946	GM12878	blood:	n/a	chr7:123885771-123885782
18	BCL11A	chr7:123885636-123885907	GM12878	blood:	n/a	n/a
19	BCLAF1	chr7:123897642-123898236	GM12878	blood:	n/a	chr7:123898197-123898206 chr7:123897901-123897910
20	BHLHE40	chr7:123885646-123885828	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:123903573-123903692	GM12878	blood:	n/a	n/a
22	BRCA1	chr7:123915746-123915818	H1-hESC	embryonic stem cell:	n/a	n/a
23	CCNT2	chr7:124019650-124019721	K562	blood:	n/a	n/a
24	CEBPB	chr7:123950894-123951209	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr7:123903472-123904002	HCT-116	colon:	n/a	chr7:123903693-123903704
26	CEBPB	chr7:123950885-123951358	HCT-116	colon:	n/a	n/a
27	CEBPB	chr7:124009369-124009705	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr7:123903383-123903885	HCT-116	colon:	n/a	chr7:123903693-123903704
29	CEBPB	chr7:123903490-123903892	IMR90	lung:	n/a	chr7:123903693-123903704
30	CEBPB	chr7:124035162-124035516	IMR90	lung:	n/a	n/a
31	CEBPB	chr7:124013810-124014125	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr7:123903524-123903881	HepG2	liver:	n/a	chr7:123903693-123903704
33	CEBPB	chr7:123950918-123951174	HepG2	liver:	n/a	n/a
34	CEBPB	chr7:124013825-124014114	A549	lung:	n/a	n/a
35	CEBPB	chr7:123903628-123903761	K562	blood:	n/a	chr7:123903693-123903704
36	CEBPB	chr7:124013892-124014116	K562	blood:	n/a	n/a
37	CEBPB	chr7:124009431-124009635	MCF-7	breast:	n/a	n/a
38	CEBPB	chr7:123901777-123902073	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr7:123903529-123903831	A549	lung:	n/a	chr7:123903693-123903704
40	CEBPB	chr7:123915569-123915830	HepG2	liver:	n/a	chr7:123915698-123915709 chr7:123915698-123915711
41	CEBPB	chr7:124013877-124014110	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr7:123903360-123903944	H1-hESC	embryonic stem cell:	n/a	chr7:123903693-123903704
43	CEBPB	chr7:124035204-124035481	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:124013792-124014147	HepG2	liver:	n/a	n/a
45	CEBPB	chr7:124006073-124006379	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:123950862-123951209	IMR90	lung:	n/a	n/a
47	CEBPB	chr7:124035154-124035475	A549	lung:	n/a	n/a
48	CEBPB	chr7:123977376-123977659	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:124013819-124014135	IMR90	lung:	n/a	n/a
50	CEBPB	chr7:124035161-124035500	H1-hESC	embryonic stem cell:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:123978181-123978231	GM12878	blood:	n/a
2	chr7:123978181-123978231	GM12892	blood:	n/a
3	chr7:123992223-123992273	ovcar-3	ovarian:	n/a
4	chr7:123992223-123992273	U87	brain:	n/a
5	chr7:123992223-123992273	HIPEpiC	eye:	n/a
6	chr7:123978181-123978231	SK-N-SH_RA	brain:	n/a
7	chr7:123992223-123992273	GM06990	blood:	n/a
8	chr7:123916407-123916457	RPTEC	kidney:	n/a
9	chr7:123916407-123916457	Caco-2	colon:	n/a
10	chr7:123978181-123978231	MCF10A-Er-Src	breast:	n/a
11	chr7:123916407-123916457	HCT-116	colon:	n/a
12	chr7:123992223-123992273	AG10803	skin:	n/a
13	chr7:123916407-123916457	HRCEpiC	kidney:	n/a
14	chr7:123992223-123992273	NB4	blood:	n/a
15	chr7:123992223-123992273	Jurkat	blood:	n/a
16	chr7:123903317-123903367	HMEC	breast:	n/a
17	chr7:123916407-123916457	SAEC	small airway:	n/a
18	chr7:123903317-123903367	SK-N-SH_RA	brain:	n/a
19	chr7:123903317-123903367	Jurkat	blood:	n/a
20	chr7:123978181-123978231	SK-N-SH	brain:	n/a
21	chr7:123916407-123916457	PANC-1	pancreas:	n/a
22	chr7:123916407-123916457	K562	blood:	n/a
23	chr7:123903317-123903367	NHBE	bronchial:	n/a
24	chr7:123903317-123903367	HIPEpiC	eye:	n/a
25	chr7:123916407-123916457	HepG2	liver:	n/a
26	chr7:123978181-123978231	HCT-116	colon:	n/a
27	chr7:123916407-123916457	SK-N-SH_RA	brain:	n/a
28	chr7:123992223-123992273	HPAEpiC	pulmonary alveolar:	n/a
29	chr7:123992223-123992273	K562	blood:	n/a
30	chr7:123903317-123903367	PFSK-1	brain:	n/a
31	chr7:123992223-123992273	SK-N-SH_RA	brain:	n/a
32	chr7:123916407-123916457	MCF10A-Er-Src	breast:	n/a
33	chr7:123992223-123992273	NH-A	brain:	n/a
34	chr7:123992223-123992273	ProgFib	skin:	n/a
35	chr7:123916407-123916457	Hepatocyte	liver:	n/a
36	chr7:123903317-123903367	SK-N-SH	brain:	n/a
37	chr7:123903317-123903367	NH-A	brain:	n/a
38	chr7:123903317-123903367	HEEpiC	esophagus:	n/a
39	chr7:123978181-123978231	U87	brain:	n/a
40	chr7:123992223-123992273	A549	lung:	n/a
41	chr7:123903317-123903367	NHDF-neo	bronchial:	n/a
42	chr7:123916407-123916457	HCM	heart:	n/a
43	chr7:123916407-123916457	AoSMC	blood vessel:	n/a
44	chr7:123916407-123916457	ProgFib	skin:	n/a
45	chr7:123903317-123903367	GM19239	blood:	n/a
46	chr7:123903317-123903367	LNCaP	prostate:	n/a
47	chr7:123992223-123992273	LNCaP	prostate:	n/a
48	chr7:123903317-123903367	MCF-7	breast:	n/a
49	chr7:123916407-123916457	HRE	kidney:	n/a
50	chr7:123992223-123992273	AG04450	lung:	fetal

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:123915423..123917674-chr7:123921407..123924592,3	K562	blood:
2	chr7:123892945..123894583-chr7:123896590..123898487,2	K562	blood:
3	chr7:123919958..123922914-chr7:123935794..123937294,2	K562	blood:
4	chr3:64234460..64234993-chr7:123973379..123973879,2	MCF-7	breast:
5	chr7:123938093..123940517-chr7:124074999..124077404,2	K562	blood:
6	chr7:123915423..123917674-chr7:123921407..123924592,3	K562	blood:
7	chr7:124018038..124020966-chr7:124025116..124027291,2	MCF-7	breast:
8	chr7:123973378..123975261-chr7:123975911..123978785,2	K562	blood:
9	chr7:124018038..124020966-chr7:124025116..124027291,2	MCF-7	breast:
10	chr7:123892945..123894583-chr7:123896590..123898487,2	K562	blood:
11	chr7:123887405..123889302-chr7:123890495..123893294,2	K562	blood:
12	chr7:123996206..123998785-chr8:77412686..77415296,2	MCF-7	breast:
13	chr7:123919958..123922914-chr7:123935794..123937294,2	K562	blood:
14	chr7:123887405..123889302-chr7:123890495..123893294,2	K562	blood:

(count:33 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM229A-2	chr7:123982515-123982615	XLOC_006591
2	lnc-TMEM229A-2	chr7:123977434-123977554	XLOC_006591
3	lnc-SPAM1-3	chr7:123993205-123993469	XLOC_006228
4	lnc-TMEM229A-1	chr7:123928853-123928911	NONHSAT123077
5	lnc-TMEM229A-2	chr7:123991905-123992154	XLOC_006591
6	lnc-SPAM1-3	chr7:123974348-123974485	XLOC_006228
7	lnc-SPAM1-3	chr7:124000163-124000252	ENSG00000242593.1
8	lnc-TMEM229A-1	chr7:123914775-123915052	NONHSAT123077
9	lnc-SPAM1-3	chr7:124027821-124028581	XLOC_006229
10	lnc-TMEM229A-1	chr7:123914733-123915052	XLOC_006590
11	lnc-SPAM1-3	chr7:124029526-124029610	ENSG00000242593.1
12	lnc-SPAM1-3	chr7:124031483-124035172	ENSG00000242593.1
13	lnc-TMEM229A-2	chr7:123989883-123989978	XLOC_006591
14	lnc-SPAM1-3	chr7:123992870-123992905	ENSG00000242593.1
15	lnc-TMEM229A-2	chr7:123982515-123982615	NR_110180
16	lnc-SPAM1-3	chr7:124032563-124032795	NONHSAT123082
17	lnc-TMEM229A-1	chr7:123927269-123927598	XLOC_006590
18	lnc-TMEM229A-1	chr7:123914775-123915052	NONHSAT123078
19	lnc-TMEM229A-2	chr7:123977434-123977554	XLOC_006591
20	lnc-SPAM1-3	chr7:124028468-124028581	ENSG00000242593.1
21	lnc-SPAM1-3	chr7:124029526-124029610	NONHSAT123082
22	lnc-TMEM229A-2	chr7:123977434-123977554	NR_110180
23	lnc-SPAM1-3	chr7:124029526-124029556	XLOC_006229
24	lnc-SPAM1-3	chr7:124028495-124028581	NONHSAT123082
25	lnc-TMEM229A-2	chr7:123991905-123992150	NR_110180
26	lnc-TMEM229A-1	chr7:123928853-123928879	NONHSAT123078
27	lnc-SPAM1-3	chr7:124016376-124016450	ENSG00000242593.1
28	lnc-TMEM229A-1	chr7:123927269-123927344	NONHSAT123078
29	lnc-TMEM229A-2	chr7:123989883-123989978	NR_110180
30	lnc-TMEM229A-2	chr7:123982515-123982615	XLOC_006591
31	lnc-SPAM1-3	chr7:124025652-124025703	ENSG00000242593.1
32	lnc-SPAM1-3	chr7:123992870-123992905	XLOC_006228
33	lnc-TMEM229A-2	chr7:123989883-123989914	XLOC_006591

No data

Variant related genes	Relation type
ENSG00000242593	TF binding region
ENSG00000243574	TF binding region
ENSG00000241324	TF binding region
ENSG00000242593	CpG island
ENSG00000243574	CpG island
ENSG00000241324	CpG island
ENSG00000242593	chromatin interactions
C6orf168	miRNA target sites

Extended variants
information (count: 2996 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2996 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200071883	chr7:123885488-123885489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374201839	chr7:123885492-123885493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567332171	chr7:123885516-123885517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541667300	chr7:123885532-123885533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185748201	chr7:123885536-123885537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572270942	chr7:123885582-123885583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576118433	chr7:123885591-123885592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188906782	chr7:123885616-123885617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532852839	chr7:123885639-123885640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549509766	chr7:123885642-123885643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs142938980	chr7:123885661-123885662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs28705785	chr7:123885750-123885751	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs531901924	chr7:123885770-123885771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548524510	chr7:123885778-123885779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552025565	chr7:123885788-123885789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568716481	chr7:123885822-123885823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs151096259	chr7:123885837-123885838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs113480422	chr7:123885877-123885878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76469441	chr7:123885894-123885895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs80243205	chr7:123885923-123885924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs143280854	chr7:123885946-123885947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550982623	chr7:123885970-123885971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576474572	chr7:123886031-123886032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567598328	chr7:123886065-123886066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146651273	chr7:123886075-123886076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs555300359	chr7:123886100-123886101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530118004	chr7:123886105-123886106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540965161	chr7:123886131-123886132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140260307	chr7:123886132-123886133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577169108	chr7:123886135-123886136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs548974052	chr7:123886146-123886147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184706485	chr7:123886164-123886165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370336299	chr7:123886208-123886209	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs563018800	chr7:123886213-123886214	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs76417045	chr7:123886249-123886250	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs542396346	chr7:123886264-123886265	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs562185817	chr7:123886297-123886298	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs527984880	chr7:123886301-123886302	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs188634116	chr7:123886322-123886323	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs534491904	chr7:123886334-123886335	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs144416096	chr7:123886349-123886350	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs181298137	chr7:123886400-123886401	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs533330174	chr7:123886448-123886449	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs12112403	chr7:123886473-123886474	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs184100067	chr7:123886486-123886487	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs535609207	chr7:123886547-123886548	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs189527940	chr7:123886549-123886550	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs565779872	chr7:123886577-123886578	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs534510709	chr7:123886620-123886621	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs557587953	chr7:123886625-123886626	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:189 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:123884600-123887200	Enhancers	HMEC	breast
2	chr7:123884800-123887200	Enhancers	NHEK	skin
3	chr7:123885400-123887200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:123885600-123886600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:123885600-123887200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:123885800-123887200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:123886000-123886200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr7:123886200-123886600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr7:123886200-123886800	Enhancers	NH-A	brain
10	chr7:123886200-123887000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr7:123886200-123887000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:123886200-123887000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr7:123886200-123887000	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr7:123886200-123887200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:123886400-123886600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:123886400-123886800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr7:123886400-123886800	Enhancers	HepG2	liver
18	chr7:123886400-123887000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr7:123886400-123887000	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr7:123886400-123887000	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr7:123886600-123887000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:123886600-123887200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr7:123887000-123887600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr7:123887200-123903600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr7:123887600-123889000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr7:123889000-123890800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:123890200-123890600	Enhancers	Fetal Lung	lung
28	chr7:123890200-123891400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr7:123890200-123892200	Enhancers	Fetal Heart	heart
30	chr7:123890600-123891600	Weak transcription	Fetal Lung	lung
31	chr7:123891400-123903200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr7:123891600-123892600	Enhancers	Fetal Lung	lung
33	chr7:123892200-123894400	Weak transcription	Fetal Heart	heart
34	chr7:123892600-123893200	Weak transcription	Fetal Lung	lung
35	chr7:123893200-123896000	Enhancers	Fetal Lung	lung
36	chr7:123894400-123894800	Enhancers	Fetal Stomach	stomach
37	chr7:123894400-123897400	Enhancers	Fetal Heart	heart
38	chr7:123894600-123895600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr7:123894800-123899600	Weak transcription	Fetal Stomach	stomach
40	chr7:123895000-123896400	Enhancers	Fetal Brain Male	brain
41	chr7:123896600-123896800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr7:123896800-123902000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr7:123897400-123897800	Flanking Active TSS	Fetal Heart	heart
44	chr7:123897400-123898200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr7:123897400-123898200	Enhancers	Hela-S3	cervix
46	chr7:123897800-123900600	Enhancers	Fetal Heart	heart
47	chr7:123898000-123898200	Enhancers	H9 Cell Line	embryonic stem cell
48	chr7:123898200-123907200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr7:123898400-123899800	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr7:123898600-123899200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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