Variant report

Variant	esv3341786
Chromosome Location	chr7:150220353-150269134
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:125)
CpG islands
(count:735)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:125 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:150267732-150267822	K562	blood:	n/a	n/a
2	CBX3	chr7:150256834-150257112	K562	blood:	n/a	n/a
3	CBX3	chr7:150256848-150257143	K562	blood:	n/a	n/a
4	CEBPB	chr7:150262346-150262711	K562	blood:	n/a	chr7:150262534-150262545
5	CEBPB	chr7:150262475-150262594	Hela-S3	cervix:	n/a	chr7:150262534-150262545
6	CEBPB	chr7:150262385-150262720	HepG2	liver:	n/a	chr7:150262534-150262545
7	CEBPB	chr7:150262403-150262688	A549	lung:	n/a	chr7:150262534-150262545
8	CEBPB	chr7:150262354-150262705	K562	blood:	n/a	chr7:150262534-150262545
9	CEBPB	chr7:150262381-150262701	H1-hESC	embryonic stem cell:	n/a	chr7:150262534-150262545
10	CEBPB	chr7:150235726-150235766	K562	blood:	n/a	n/a
11	CEBPB	chr7:150262477-150262657	K562	blood:	n/a	chr7:150262534-150262545
12	CEBPB	chr7:150235713-150235754	A549	lung:	n/a	n/a
13	CEBPB	chr7:150262392-150262657	IMR90	lung:	n/a	chr7:150262534-150262545
14	CEBPB	chr7:150268399-150268473	K562	blood:	n/a	n/a
15	CTCF	chr7:150221240-150221390	GM12866	blood:	n/a	n/a
16	CTCF	chr7:150265891-150266001	Spleen_OC	spleen:	n/a	n/a
17	CTCF	chr7:150265953-150265983	GM12878	blood:	n/a	n/a
18	CTCF	chr7:150256454-150256532	GM20000	blood:	n/a	n/a
19	CTCF	chr7:150230180-150230330	GM12873	blood:	n/a	n/a
20	CTCF	chr7:150221280-150221430	GM12873	blood:	n/a	n/a
21	CTCF	chr7:150230289-150230303	GM12892	blood:	n/a	n/a
22	CTCF	chr7:150266502-150266593	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr7:150221260-150221410	HepG2	liver:	n/a	n/a
24	CTCF	chr7:150265880-150266030	GM12875	blood:	n/a	n/a
25	CTCF	chr7:150230194-150230279	GM12878	blood:	n/a	n/a
26	CTCF	chr7:150256510-150256563	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr7:150221240-150221390	GM06990	blood:	n/a	n/a
28	CTCF	chr7:150230209-150230280	K562	blood:	n/a	n/a
29	CTCF	chr7:150224116-150224140	Lung_OC	lung:	n/a	n/a
30	CTCF	chr7:150221260-150221410	GM12864	blood:	n/a	n/a
31	CTCF	chr7:150237030-150237048	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr7:150265874-150265958	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr7:150257660-150257810	SAEC	small airway:	n/a	n/a
34	CTCF	chr7:150268549-150268584	Lung_OC	lung:	n/a	n/a
35	CTCF	chr7:150252478-150252552	Lung_OC	lung:	n/a	n/a
36	CTCF	chr7:150221320-150221348	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr7:150257660-150257810	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr7:150221200-150221350	GM12875	blood:	n/a	n/a
39	CTCF	chr7:150248655-150248734	Fibrobl	skin:	n/a	n/a
40	CTCF	chr7:150265920-150266070	GM12865	blood:	n/a	n/a
41	CTCF	chr7:150221125-150221401	H1-hESC	embryonic stem cell:	n/a	n/a
42	EBF1	chr7:150254264-150254411	GM12878	blood:	n/a	n/a
43	EBF1	chr7:150265699-150265895	GM12878	blood:	n/a	chr7:150265796-150265807
44	ELF1	chr7:150232962-150233283	GM12878	blood:	n/a	n/a
45	EP300	chr7:150256101-150256183	K562	blood:	n/a	n/a
46	FOS	chr7:150263827-150263902	MCF10A-Er-Src	breast:	n/a	chr7:150263864-150263872 chr7:150263862-150263874 chr7:150263864-150263871 chr7:150263863-150263873 chr7:150263863-150263872
47	FOS	chr7:150259824-150260877	HUVEC	blood vessel:	n/a	n/a
48	FOS	chr7:150260963-150261435	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr7:150263803-150264462	HUVEC	blood vessel:	n/a	chr7:150263864-150263872 chr7:150263862-150263874 chr7:150263864-150263871 chr7:150263863-150263873 chr7:150263863-150263872
50	GATA2	chr7:150253524-150254182	HUVEC	blood vessel:	n/a	chr7:150253997-150254011

(count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150263322-150263372	SKMC	muscle:	n/a
2	chr7:150264987-150265037	GM12891	blood:	n/a
3	chr7:150263322-150263372	SAEC	small airway:	n/a
4	chr7:150263322-150263372	SKMC	muscle:	n/a
5	chr7:150264987-150265037	GM12891	blood:	n/a
6	chr7:150263322-150263372	SAEC	small airway:	n/a
7	chr7:150253908-150253958	MCF-7	breast:	n/a
8	chr7:150232206-150232256	PFSK-1	brain:	n/a
9	chr7:150263087-150263137	ProgFib	skin:	n/a
10	chr7:150263087-150263137	A549	lung:	n/a
11	chr7:150264311-150264361	SAEC	small airway:	n/a
12	chr7:150233184-150233234	HIPEpiC	eye:	n/a
13	chr7:150264767-150264817	AG04449	skin:	fetal
14	chr7:150264284-150264334	SK-N-SH	brain:	n/a
15	chr7:150263322-150263372	AG09319	gingival:	n/a
16	chr7:150233184-150233234	PrEC	prostate:	n/a
17	chr7:150263087-150263137	AG10803	skin:	n/a
18	chr7:150263322-150263372	SK-N-MC	brain:	n/a
19	chr7:150263322-150263372	HUVEC	blood vessel:	n/a
20	chr7:150253908-150253958	U87	brain:	n/a
21	chr7:150264987-150265037	SAEC	small airway:	n/a
22	chr7:150264987-150265037	SK-N-SH	brain:	n/a
23	chr7:150253908-150253958	HRCEpiC	kidney:	n/a
24	chr7:150253908-150253958	GM19239	blood:	n/a
25	chr7:150264284-150264334	SKMC	muscle:	n/a
26	chr7:150264767-150264817	AG09319	gingival:	n/a
27	chr7:150253908-150253958	Jurkat	blood:	n/a
28	chr7:150254026-150254076	NH-A	brain:	n/a
29	chr7:150253908-150253958	HRE	kidney:	n/a
30	chr7:150264284-150264334	MCF-7	breast:	n/a
31	chr7:150263087-150263137	MCF10A-Er-Src	breast:	n/a
32	chr7:150264767-150264817	BE2_C	brain:	n/a
33	chr7:150263322-150263372	HPAEpiC	pulmonary alveolar:	n/a
34	chr7:150263087-150263137	NH-A	brain:	n/a
35	chr7:150263087-150263137	Caco-2	colon:	n/a
36	chr7:150253908-150253958	SKMC	muscle:	n/a
37	chr7:150264284-150264334	BE2_C	brain:	n/a
38	chr7:150233184-150233234	NHBE	bronchial:	n/a
39	chr7:150264284-150264334	GM19239	blood:	n/a
40	chr7:150232206-150232256	HUVEC	blood vessel:	n/a
41	chr7:150264767-150264817	GM12892	blood:	n/a
42	chr7:150262075-150262125	BJ	skin:	n/a
43	chr7:150263087-150263137	HMEC	breast:	n/a
44	chr7:150264284-150264334	MCF10A-Er-Src	breast:	n/a
45	chr7:150264767-150264817	GM06990	blood:	n/a
46	chr7:150232206-150232256	MCF-7	breast:	n/a
47	chr7:150232206-150232256	K562	blood:	n/a
48	chr7:150262075-150262125	CMK	blood:	n/a
49	chr7:150253908-150253958	HEEpiC	esophagus:	n/a
50	chr7:150254026-150254076	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:150232590..150235233-chr7:150277857..150280710,2	K562	blood:
2	chr7:150221183..150223870-chr7:150226440..150228746,2	K562	blood:
3	chr7:150221183..150223870-chr7:150226440..150228746,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GIMAP6-3	chr7:150238842-150239186	NONHSAT124143

No data

Variant related genes	Relation type
GIMAP4	TF binding region
ALDH7A1P3	TF binding region
GIMAP4	CpG island
ALDH7A1P3	CpG island

Extended variants
information (count: 1555 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1555 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532404880	chr7:150220365-150220366	Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs546449107	chr7:150220422-150220423	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs375392879	chr7:150220423-150220424	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs563056443	chr7:150220433-150220434	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs531918947	chr7:150220467-150220468	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs182213326	chr7:150220469-150220470	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs184311696	chr7:150220471-150220472	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs189208630	chr7:150220507-150220508	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs143961422	chr7:150220520-150220521	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs181092820	chr7:150220539-150220540	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs547518491	chr7:150220620-150220621	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs185881425	chr7:150220631-150220632	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs566611943	chr7:150220654-150220655	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs146427796	chr7:150220661-150220662	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs149051583	chr7:150220691-150220692	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs190598534	chr7:150220694-150220695	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs535637281	chr7:150220710-150220711	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs143093616	chr7:150220745-150220746	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs113912940	chr7:150220771-150220772	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs140575863	chr7:150220786-150220787	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs370575776	chr7:150220795-150220796	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs553871709	chr7:150220798-150220799	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs62501527	chr7:150220815-150220816	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs11769223	chr7:150220845-150220846	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs138516199	chr7:150220846-150220847	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs531951529	chr7:150220855-150220856	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs573432756	chr7:150220875-150220876	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs7793974	chr7:150220876-150220877	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs527906533	chr7:150220880-150220881	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs11772952	chr7:150220886-150220887	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs574109205	chr7:150220887-150220888	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs373143226	chr7:150220904-150220905	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs549559705	chr7:150220926-150220927	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs56408434	chr7:150220955-150220956	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs73482304	chr7:150220974-150220975	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs548872111	chr7:150220984-150220985	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs565510467	chr7:150221027-150221028	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs557139581	chr7:150221059-150221060	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs79123541	chr7:150221082-150221083	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs181703248	chr7:150221137-150221138	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs570307350	chr7:150221169-150221170	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs7794415	chr7:150221197-150221198	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs556243659	chr7:150221234-150221235	Enhancers ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs146320267	chr7:150221276-150221277	Enhancers ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs187100202	chr7:150221314-150221315	Enhancers ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs192166883	chr7:150221315-150221316	Enhancers ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs572659117	chr7:150221400-150221401	Enhancers ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs35382955	chr7:150221408-150221409	Enhancers ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs541672062	chr7:150221409-150221410	Enhancers ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs73726889	chr7:150221414-150221415	Enhancers ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:88)

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
Wilms tumour	21544195	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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:603 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150218000-150220800	Weak transcription	HUVEC	blood vessel
2	chr7:150219000-150220600	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr7:150219200-150220400	Active TSS	Primary T cells from cord blood	blood
4	chr7:150219200-150220800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr7:150219200-150221000	Weak transcription	Fetal Thymus	thymus
6	chr7:150219200-150221000	Weak transcription	Dnd41	blood
7	chr7:150219200-150221000	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr7:150219200-150221200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr7:150219200-150221200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr7:150219200-150222400	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
11	chr7:150219400-150220400	Genic enhancers	Primary T cells fromperipheralblood	blood
12	chr7:150219400-150220600	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr7:150219400-150221000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr7:150219800-150220800	Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr7:150219800-150222400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr7:150220000-150220400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr7:150220000-150221000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr7:150220000-150221000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr7:150220000-150221600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr7:150220200-150221000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr7:150220200-150221000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr7:150220200-150221000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr7:150220200-150221400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:150220200-150221600	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr7:150220200-150222800	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr7:150220400-150221000	Weak transcription	Primary T cells from cord blood	blood
27	chr7:150220400-150221200	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr7:150220400-150221600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr7:150220600-150221400	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr7:150220800-150221600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr7:150221000-150221400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr7:150221000-150221600	Enhancers	H1 Cell Line	embryonic stem cell
33	chr7:150221000-150221600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr7:150221000-150221600	Enhancers	Primary T cells from cord blood	blood
35	chr7:150221000-150221600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr7:150221000-150222200	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
37	chr7:150221200-150221400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
38	chr7:150221200-150221600	Enhancers	H9 Cell Line	embryonic stem cell
39	chr7:150221200-150221600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr7:150221200-150221600	Active TSS	Small Intestine	intestine
41	chr7:150221200-150221800	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
42	chr7:150221200-150222200	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
43	chr7:150221200-150222400	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
44	chr7:150221200-150223000	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr7:150221400-150223200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr7:150221600-150222000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr7:150221600-150223400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr7:150221600-150224600	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr7:150222000-150223200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr7:150222200-150222400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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