Variant report

Variant	esv1824658
Chromosome Location	chr7:101970299-102004364
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1186)
CpG islands
(count:549)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1186 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102004022-102004495	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102004087-102004234	K562	blood:	n/a	n/a
3	ATF1	chr7:102003979-102004409	K562	blood:	n/a	n/a
4	ATF2	chr7:102003966-102004343	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:102003964-102004508	GM12878	blood:	n/a	n/a
6	ATF3	chr7:102004002-102004510	A549	lung:	n/a	n/a
7	ATF3	chr7:102003901-102004509	A549	lung:	n/a	n/a
8	ATF3	chr7:102004112-102004430	K562	blood:	n/a	n/a
9	BACH1	chr7:102004065-102004493	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:101983890-101984191	GM12878	blood:	n/a	n/a
11	BATF	chr7:101997012-101997266	GM12878	blood:	n/a	n/a
12	BATF	chr7:101982483-101982724	GM12878	blood:	n/a	n/a
13	BATF	chr7:101995463-101995686	GM12878	blood:	n/a	n/a
14	BATF	chr7:101980953-101981449	GM12878	blood:	n/a	n/a
15	BATF	chr7:101999193-101999814	GM12878	blood:	n/a	n/a
16	BATF	chr7:101997851-101998066	GM12878	blood:	n/a	n/a
17	BATF	chr7:101977330-101977583	GM12878	blood:	n/a	n/a
18	BATF	chr7:102004126-102004439	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:101983613-101984160	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:101983656-101983848	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:101982462-101982707	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:101987225-101987383	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:101975677-101976058	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:101975878-101976049	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:101999319-101999808	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:101992379-101992526	GM12878	blood:	n/a	n/a
27	BCL11A	chr7:101997984-101998246	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:101994622-101994770	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:102003720-102004191	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:101987793-101988042	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:101990402-101990553	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:101997514-101997663	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:101982419-101982753	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:101983901-101984172	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:102003799-102003974	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:101996913-101997326	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:101981186-101981393	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:101977204-101977363	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:101981081-101981468	GM12878	blood:	n/a	n/a
40	BCL11A	chr7:101999465-101999748	GM12878	blood:	n/a	n/a
41	BCL3	chr7:102003976-102004358	A549	lung:	n/a	n/a
42	BCLAF1	chr7:102003908-102004427	GM12878	blood:	n/a	n/a
43	BCLAF1	chr7:102003953-102004478	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:102004109-102004495	GM12878	blood:	n/a	n/a
45	BHLHE40	chr7:102004102-102004486	HepG2	liver:	n/a	n/a
46	BHLHE40	chr7:101997473-101997748	HepG2	liver:	n/a	n/a
47	BHLHE40	chr7:102004011-102004495	K562	blood:	n/a	n/a
48	BRCA1	chr7:102004018-102004395	Hela-S3	cervix:	n/a	n/a
49	CBX3	chr7:102003731-102004487	K562	blood:	n/a	n/a
50	CBX3	chr7:102003667-102004553	K562	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101989013-101989063	LNCaP	prostate:	n/a
2	chr7:101998514-101998564	AoSMC	blood vessel:	n/a
3	chr7:101999041-101999091	NHBE	bronchial:	n/a
4	chr7:101999041-101999091	SK-N-MC	brain:	n/a
5	chr7:102004298-102004348	K562	blood:	n/a
6	chr7:101986487-101986537	MCF-7	breast:	n/a
7	chr7:102004298-102004348	HIPEpiC	eye:	n/a
8	chr7:101999041-101999091	H1-hESC	embryonic stem cell:	embryo
9	chr7:101986487-101986537	HMEC	breast:	n/a
10	chr7:101986487-101986537	ECC-1	luminal epithelium:	n/a
11	chr7:101972144-101972194	HIPEpiC	eye:	n/a
12	chr7:102004098-102004148	RPTEC	kidney:	n/a
13	chr7:101989013-101989063	HUVEC	blood vessel:	n/a
14	chr7:101998514-101998564	AG04450	lung:	fetal
15	chr7:101986487-101986537	SKMC	muscle:	n/a
16	chr7:101989034-101989084	HCT-116	colon:	n/a
17	chr7:101999041-101999091	LNCaP	prostate:	n/a
18	chr7:101986487-101986537	IMR90	lung:	fetal
19	chr7:101972144-101972194	A549	lung:	n/a
20	chr7:102004298-102004348	HCM	heart:	n/a
21	chr7:101998514-101998564	SK-N-MC	brain:	n/a
22	chr7:101989034-101989084	Caco-2	colon:	n/a
23	chr7:101986487-101986537	AG04450	lung:	fetal
24	chr7:101999041-101999091	HIPEpiC	eye:	n/a
25	chr7:101999041-101999091	AG09319	gingival:	n/a
26	chr7:102004098-102004148	U87	brain:	n/a
27	chr7:101989013-101989063	Hela-S3	cervix:	n/a
28	chr7:101991189-101991239	SAEC	small airway:	n/a
29	chr7:101991189-101991239	AG09309	skin:	n/a
30	chr7:101989013-101989063	HCF	heart:	n/a
31	chr7:102004098-102004148	ECC-1	luminal epithelium:	n/a
32	chr7:101999041-101999091	U87	brain:	n/a
33	chr7:101972144-101972194	HepG2	liver:	n/a
34	chr7:101986487-101986537	HEEpiC	esophagus:	n/a
35	chr7:101989013-101989063	GM12891	blood:	n/a
36	chr7:101989013-101989063	PANC-1	pancreas:	n/a
37	chr7:101986487-101986537	HCT-116	colon:	n/a
38	chr7:101989034-101989084	CMK	blood:	n/a
39	chr7:101998514-101998564	NHBE	bronchial:	n/a
40	chr7:101991189-101991239	HRE	kidney:	n/a
41	chr7:101999041-101999091	HAEpiC	amniotic membrane:	n/a
42	chr7:101991189-101991239	RPTEC	kidney:	n/a
43	chr7:101991189-101991239	Hepatocyte	liver:	n/a
44	chr7:101991189-101991239	CMK	blood:	n/a
45	chr7:102004298-102004348	HUVEC	blood vessel:	n/a
46	chr7:101998514-101998564	HepG2	liver:	n/a
47	chr7:101989034-101989084	Jurkat	blood:	n/a
48	chr7:101989013-101989063	BJ	skin:	n/a
49	chr7:101989013-101989063	SKMC	muscle:	n/a
50	chr7:101972144-101972194	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:101969853..101972657-chr7:102004064..102005598,2	MCF-7	breast:
2	chr7:101969853..101972657-chr7:102004064..102005598,2	MCF-7	breast:
3	chr7:101962260..101964912-chr7:101971375..101973484,2	MCF-7	breast:
4	chr7:101927779..101934386-chr7:102001430..102005829,12	MCF-7	breast:
5	chr7:101965469..101968383-chr7:101972225..101973731,2	K562	blood:
6	chr17:41465686..41466379-chr7:102004292..102004823,2	NB4	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKRIP1-1	chr7:101995384-101995807	ENSG00000259313.1
2	lnc-PRKRIP1-1	chr7:101993676-101993848	ENSG00000259313.1

No data

Variant related genes	Relation type
ENSG00000228546	TF binding region
ENSG00000200552	TF binding region
ENSG00000239969	TF binding region
SPDYE6	TF binding region
PRKRIP1	TF binding region
ENSG00000170409	TF binding region
ENSG00000228546	CpG island
ENSG00000200552	CpG island
ENSG00000239969	CpG island
SPDYE6	CpG island
PRKRIP1	CpG island
ENSG00000170409	CpG island
ENSG00000128563	chromatin interactions
ENSG00000160999	chromatin interactions
ENSG00000239969	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000170409	chromatin interactions

Extended variants
information (count: 1004 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1004 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117729532	chr7:101970326-101970327	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs562010237	chr7:101970332-101970333	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs540372386	chr7:101970360-101970361	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs565038928	chr7:101970380-101970381	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs142923967	chr7:101970381-101970382	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs562920513	chr7:101970387-101970388	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs803114	chr7:101970399-101970400	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs140234852	chr7:101970408-101970409	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs567157754	chr7:101970424-101970425	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs558506649	chr7:101970438-101970439	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs186467273	chr7:101970446-101970447	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs191249434	chr7:101970469-101970470	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs374782826	chr7:101970470-101970471	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs367899875	chr7:101970477-101970478	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs192539850	chr7:101970515-101970516	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs537576219	chr7:101970522-101970523	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs555736071	chr7:101970571-101970572	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs577258390	chr7:101970617-101970618	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs538253322	chr7:101970638-101970639	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs145239030	chr7:101970706-101970707	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs137897961	chr7:101970708-101970709	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs571934496	chr7:101970755-101970756	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs114006299	chr7:101970774-101970775	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs141097410	chr7:101970812-101970813	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs182926831	chr7:101970840-101970841	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs544760079	chr7:101970842-101970843	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs144847097	chr7:101970857-101970858	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs114640587	chr7:101970913-101970914	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs138771061	chr7:101970964-101970965	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs560590746	chr7:101970975-101970976	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs2694165	chr7:101971043-101971044	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs549288131	chr7:101971175-101971176	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs567895662	chr7:101971197-101971198	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs187339312	chr7:101971199-101971200	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs144553798	chr7:101971206-101971207	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs571010712	chr7:101971255-101971256	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs548884999	chr7:101971279-101971280	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs77424850	chr7:101971284-101971285	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs112639791	chr7:101971295-101971296	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs191075897	chr7:101971334-101971335	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs183166124	chr7:101971344-101971345	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs117165749	chr7:101971353-101971354	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs567477729	chr7:101971355-101971356	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs9692601	chr7:101971447-101971448	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs188009782	chr7:101971486-101971487	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs192378312	chr7:101971490-101971491	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs184334905	chr7:101971504-101971505	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs578156011	chr7:101971529-101971530	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs545059784	chr7:101971552-101971553	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs201201546	chr7:101971567-101971568	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Cancer	19907438	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:198 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101944000-101975400	Weak transcription	Right Atrium	heart
2	chr7:101962000-101973200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:101962800-101970800	Weak transcription	GM12878-XiMat	blood
4	chr7:101962800-101971600	Weak transcription	Primary B cells from cord blood	blood
5	chr7:101963200-101971600	Weak transcription	Primary B cells from peripheral blood	blood
6	chr7:101963800-101971600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:101968000-101975400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:101969200-101972200	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr7:101970000-101972000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr7:101970800-101971800	Enhancers	GM12878-XiMat	blood
11	chr7:101971600-101971800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:101971600-101972600	Enhancers	Primary B cells from cord blood	blood
13	chr7:101971600-101972800	Enhancers	Primary B cells from peripheral blood	blood
14	chr7:101971800-101972200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr7:101971800-101972600	Flanking Active TSS	GM12878-XiMat	blood
16	chr7:101971800-101974200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr7:101972200-101972400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr7:101972200-101972400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr7:101972200-101972600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr7:101972200-101972600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr7:101972200-101972800	Enhancers	H1 Cell Line	embryonic stem cell
22	chr7:101972200-101972800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr7:101972200-101973400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr7:101972400-101972600	Enhancers	Fetal Kidney	kidney
25	chr7:101972600-101973400	Enhancers	GM12878-XiMat	blood
26	chr7:101972600-101973600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr7:101972800-101973600	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr7:101972800-101973800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr7:101972800-101980800	Weak transcription	Primary B cells from peripheral blood	blood
30	chr7:101973200-101973600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr7:101973400-101973600	Enhancers	Fetal Kidney	kidney
32	chr7:101973400-101974200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr7:101973400-101975200	Weak transcription	GM12878-XiMat	blood
34	chr7:101973600-101974200	Enhancers	H1 Cell Line	embryonic stem cell
35	chr7:101973600-101974800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr7:101973800-101974000	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr7:101973800-101974000	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr7:101974200-101974800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr7:101974800-101975000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr7:101974800-101975000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr7:101975000-101976400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr7:101975200-101976200	Enhancers	GM12878-XiMat	blood
43	chr7:101975400-101977200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr7:101976200-101981000	Weak transcription	GM12878-XiMat	blood
45	chr7:101980800-101983800	Enhancers	Primary B cells from peripheral blood	blood
46	chr7:101981000-101981800	Enhancers	GM12878-XiMat	blood
47	chr7:101981400-101981800	Enhancers	Primary B cells from cord blood	blood
48	chr7:101981800-101986000	Weak transcription	GM12878-XiMat	blood
49	chr7:101987400-102003800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr7:101987600-101990600	Weak transcription	Primary neutrophils fromperipheralblood	blood

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