Variant report

Variant	esv1817757
Chromosome Location	chr7:99896488-99935709
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1020)
CpG islands
(count:1527)
Chromatin interactive
region (count:19)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1020 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:99933514-99933890	K562	blood:	n/a	n/a
2	ATF2	chr7:99933587-99933979	GM12878	blood:	n/a	n/a
3	BACH1	chr7:99933388-99934007	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr7:99922916-99923120	GM12878	blood:	n/a	n/a
5	BATF	chr7:99901300-99901503	GM12878	blood:	n/a	n/a
6	BATF	chr7:99915667-99915855	GM12878	blood:	n/a	n/a
7	BATF	chr7:99902075-99902343	GM12878	blood:	n/a	n/a
8	BATF	chr7:99901285-99901496	GM12878	blood:	n/a	n/a
9	BATF	chr7:99933508-99933915	GM12878	blood:	n/a	n/a
10	BATF	chr7:99902780-99903057	GM12878	blood:	n/a	n/a
11	BATF	chr7:99900740-99901050	GM12878	blood:	n/a	n/a
12	BATF	chr7:99931789-99932008	GM12878	blood:	n/a	n/a
13	BATF	chr7:99921263-99921667	GM12878	blood:	n/a	n/a
14	BATF	chr7:99933104-99933496	GM12878	blood:	n/a	n/a
15	BATF	chr7:99900718-99901136	GM12878	blood:	n/a	n/a
16	BATF	chr7:99902062-99903018	GM12878	blood:	n/a	n/a
17	BATF	chr7:99922294-99922458	GM12878	blood:	n/a	n/a
18	BATF	chr7:99931763-99932072	GM12878	blood:	n/a	n/a
19	BATF	chr7:99932699-99932942	GM12878	blood:	n/a	n/a
20	BATF	chr7:99902374-99902726	GM12878	blood:	n/a	n/a
21	BATF	chr7:99921172-99921850	GM12878	blood:	n/a	n/a
22	BATF	chr7:99931291-99931464	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:99901627-99901859	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:99929074-99929275	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:99922824-99923053	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:99922866-99923130	GM12878	blood:	n/a	n/a
27	BCL11A	chr7:99900777-99901048	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:99899365-99899765	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:99921092-99921910	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:99931290-99931519	GM12878	blood:	n/a	chr7:99931369-99931378
31	BCL11A	chr7:99902046-99902591	GM12878	blood:	n/a	chr7:99902302-99902311
32	BCL11A	chr7:99915597-99915943	GM12878	blood:	n/a	chr7:99915669-99915678
33	BCL11A	chr7:99921061-99921746	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:99931855-99932416	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:99902728-99903004	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:99922169-99922589	GM12878	blood:	n/a	chr7:99922216-99922225
37	BCL11A	chr7:99915598-99915786	GM12878	blood:	n/a	chr7:99915669-99915678
38	BCL11A	chr7:99901601-99901842	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:99931278-99931549	GM12878	blood:	n/a	chr7:99931369-99931378
40	BCL11A	chr7:99933106-99934023	GM12878	blood:	n/a	chr7:99933249-99933262
41	BCL11A	chr7:99902084-99902502	GM12878	blood:	n/a	chr7:99902302-99902311
42	BCL11A	chr7:99931741-99932177	GM12878	blood:	n/a	n/a
43	BCL11A	chr7:99933147-99933368	GM12878	blood:	n/a	chr7:99933249-99933262
44	BCL11A	chr7:99899420-99899769	GM12878	blood:	n/a	n/a
45	BCL11A	chr7:99903987-99904347	GM12878	blood:	n/a	n/a
46	BCL11A	chr7:99900720-99901137	GM12878	blood:	n/a	n/a
47	BCL3	chr7:99933337-99933993	A549	lung:	n/a	n/a
48	BCL3	chr7:99933691-99934093	A549	lung:	n/a	n/a
49	BCLAF1	chr7:99933315-99933964	GM12878	blood:	n/a	n/a
50	BHLHE40	chr7:99933565-99933968	K562	blood:	n/a	n/a

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99912131-99912181	SKMC	muscle:	n/a
2	chr7:99929438-99929488	SK-N-SH	brain:	n/a
3	chr7:99912131-99912181	SKMC	muscle:	n/a
4	chr7:99929438-99929488	SK-N-SH	brain:	n/a
5	chr7:99934006-99934056	HAEpiC	amniotic membrane:	n/a
6	chr7:99933428-99933478	K562	blood:	n/a
7	chr7:99912131-99912181	PFSK-1	brain:	n/a
8	chr7:99933670-99933720	HEK293	kidney:	embryo
9	chr7:99934001-99934051	AG04449	skin:	fetal
10	chr7:99933530-99933580	AG09309	skin:	n/a
11	chr7:99935133-99935183	PrEC	prostate:	n/a
12	chr7:99933968-99934018	PrEC	prostate:	n/a
13	chr7:99933968-99934018	HRPEpiC	eye:	n/a
14	chr7:99918120-99918170	U87	brain:	n/a
15	chr7:99904875-99904925	Hepatocyte	liver:	n/a
16	chr7:99935381-99935431	RPTEC	kidney:	n/a
17	chr7:99932089-99932139	GM12892	blood:	n/a
18	chr7:99933543-99933593	HUVEC	blood vessel:	n/a
19	chr7:99904850-99904900	BJ	skin:	n/a
20	chr7:99934059-99934109	AG09309	skin:	n/a
21	chr7:99918120-99918170	ProgFib	skin:	n/a
22	chr7:99933428-99933478	HIPEpiC	eye:	n/a
23	chr7:99933548-99933598	NT2-D1	testis:	n/a
24	chr7:99933797-99933847	LNCaP	prostate:	n/a
25	chr7:99904850-99904900	HL-60	blood:	n/a
26	chr7:99933543-99933593	HNPCEpiC	eye:	n/a
27	chr7:99935177-99935227	MCF10A-Er-Src	breast:	n/a
28	chr7:99918120-99918170	AG04450	lung:	fetal
29	chr7:99935133-99935183	GM12891	blood:	n/a
30	chr7:99933968-99934018	HAEpiC	amniotic membrane:	n/a
31	chr7:99933968-99934018	NB4	blood:	n/a
32	chr7:99933717-99933767	AG09309	skin:	n/a
33	chr7:99934006-99934056	AG10803	skin:	n/a
34	chr7:99935133-99935183	NH-A	brain:	n/a
35	chr7:99905334-99905384	RPTEC	kidney:	n/a
36	chr7:99933797-99933847	HIPEpiC	eye:	n/a
37	chr7:99935381-99935431	HPAEpiC	pulmonary alveolar:	n/a
38	chr7:99933501-99933551	NB4	blood:	n/a
39	chr7:99933548-99933598	HAEpiC	amniotic membrane:	n/a
40	chr7:99933968-99934018	K562	blood:	n/a
41	chr7:99933717-99933767	HNPCEpiC	eye:	n/a
42	chr7:99929438-99929488	NHBE	bronchial:	n/a
43	chr7:99935177-99935227	HPAEpiC	pulmonary alveolar:	n/a
44	chr7:99904875-99904925	MCF10A-Er-Src	breast:	n/a
45	chr7:99933543-99933593	SAEC	small airway:	n/a
46	chr7:99933721-99933771	T-47D	breast:	n/a
47	chr7:99933968-99934018	BE2_C	brain:	n/a
48	chr7:99929438-99929488	CMK	blood:	n/a
49	chr7:99933530-99933580	AG04450	lung:	fetal
50	chr7:99933797-99933847	HL-60	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99933293..99933992-chr7:130794505..130795164,2	Hela-S3	cervix:
2	chr5:36876650..36877236-chr7:99933531..99934342,2	Hela-S3	cervix:
3	chr6:7909845..7910649-chr7:99932993..99933972,2	Hela-S3	cervix:
4	chr7:99932595..99935080-chr7:100025979..100028387,3	K562	blood:
5	chr7:99932349..99935076-chr7:100025979..100028387,3	K562	blood:
6	chr11:18416119..18416955-chr7:99933156..99933912,2	Hela-S3	cervix:
7	chr7:99931911..99935442-chr7:99938364..99941933,5	MCF-7	breast:
8	chr7:99933746..99935432-chr7:100238068..100240501,2	K562	blood:
9	chr6:26216777..26217754-chr7:99933218..99933721,2	Hela-S3	cervix:
10	chr1:35658693..35659210-chr7:99933428..99934253,2	Hela-S3	cervix:
11	chr7:99935191..99937909-chr7:99939169..99942843,3	K562	blood:
12	chr7:99932234..99937909-chr7:99939373..99942446,6	K562	blood:
13	chr6:90539369..90540027-chr7:99932976..99933753,2	Hela-S3	cervix:
14	chr7:66767136..66768124-chr7:99933487..99934025,2	HCT-116	colon:
15	chr7:99765936..99768056-chr7:99933468..99935315,2	MCF-7	breast:
16	chr7:99933438..99934039-chr7:100026430..100027170,2	NB4	blood:
17	chr7:99932318..99935048-chr7:100026420..100028378,2	MCF-7	breast:
18	chr7:6048837..6049368-chr7:99933514..99934016,2	Hela-S3	cervix:
19	chr7:99715815..99718290-chr7:99932504..99934640,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PILRB-1	chr7:99933737-99933960	NONHSAT122358
2	lnc-GATS-3	chr7:99927647-99927907	NONHSAT122354
3	lnc-GATS-3	chr7:99928086-99928176	NONHSAT122354
4	lnc-GATS-1	chr7:99907941-99908299	expReg_chr7_6426_-
5	lnc-PILRB-1	chr7:99935200-99935637	NONHSAT122361
6	lnc-GATS-2	chr7:99913916-99914300	expReg_chr7_6439_-

No data

Variant related genes	Relation type
PMS2P1	TF binding region
STAG3L5P	TF binding region
PILRB	TF binding region
SPDYE3	TF binding region
STAG3L5P-PVRIG2P-PILRB	TF binding region
ENSG00000201913	TF binding region
PMS2P1	CpG island
STAG3L5P	CpG island
PILRB	CpG island
SPDYE3	CpG island
STAG3L5P-PVRIG2P-PILRB	CpG island
ENSG00000201913	CpG island
ENSG00000164190	chromatin interactions
ENSG00000187990	chromatin interactions
ENSG00000197093	chromatin interactions
ENSG00000239264	chromatin interactions
ENSG00000106610	chromatin interactions
ENSG00000134333	chromatin interactions
ENSG00000118412	chromatin interactions
ENSG00000116560	chromatin interactions
ENSG00000067601	chromatin interactions
ENSG00000166997	chromatin interactions
ENSG00000128585	chromatin interactions
ENSG00000106305	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000168274	chromatin interactions
ENSG00000106327	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000078319	chromatin interactions
ENSG00000231721	chromatin interactions
ENSG00000106290	chromatin interactions

Extended variants
information (count: 1190 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1190 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187635341	chr7:99896519-99896520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552868935	chr7:99896520-99896521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570891904	chr7:99896546-99896547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534993689	chr7:99896564-99896565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553236228	chr7:99896656-99896657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs193127437	chr7:99896661-99896662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549369958	chr7:99896716-99896717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535536389	chr7:99896717-99896718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554343413	chr7:99896722-99896723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575800897	chr7:99896742-99896743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs111842263	chr7:99896754-99896755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs184179816	chr7:99896794-99896795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543348519	chr7:99896815-99896816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564817178	chr7:99896842-99896843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370409167	chr7:99896877-99896878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs201720480	chr7:99896886-99896887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541013162	chr7:99896907-99896908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559047277	chr7:99896915-99896916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529800519	chr7:99896941-99896942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548279792	chr7:99896977-99896978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563888296	chr7:99897017-99897018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531110057	chr7:99897065-99897066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368351363	chr7:99897166-99897167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142648002	chr7:99897183-99897184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571119688	chr7:99897195-99897196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528515441	chr7:99897241-99897242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546979688	chr7:99897253-99897254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549865120	chr7:99897254-99897255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532111222	chr7:99897286-99897287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372048546	chr7:99897308-99897309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189322783	chr7:99897342-99897343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557021775	chr7:99897376-99897377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569545372	chr7:99897377-99897378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536845968	chr7:99897387-99897388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181315321	chr7:99897404-99897405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183975180	chr7:99897424-99897425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577077851	chr7:99897425-99897426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540923386	chr7:99897451-99897452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147248866	chr7:99897475-99897476	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
40	rs188706691	chr7:99897488-99897489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541980616	chr7:99897508-99897509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181517281	chr7:99897524-99897525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531174437	chr7:99897540-99897541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546407395	chr7:99897598-99897599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564480255	chr7:99897605-99897606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs71569560	chr7:99897628-99897629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538703903	chr7:99897678-99897679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528783039	chr7:99897759-99897760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192234310	chr7:99897792-99897793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182313548	chr7:99897803-99897804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Stenocardia	21860640	CNVD
Vasospasm	21860640	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
Acute lymphoblastic leukemia	21339820	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
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:871 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99870200-99916800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr7:99870200-99932800	Weak transcription	Ovary	ovary
3	chr7:99870400-99901600	Weak transcription	Thymus	Thymus
4	chr7:99870400-99904600	Weak transcription	Fetal Muscle Trunk	muscle
5	chr7:99870400-99917000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr7:99870400-99917000	Weak transcription	Fetal Muscle Leg	muscle
7	chr7:99870400-99917600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:99870400-99923400	Weak transcription	Fetal Intestine Large	intestine
9	chr7:99870400-99932600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr7:99870600-99898800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr7:99870600-99904600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr7:99870600-99916800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr7:99870600-99923400	Weak transcription	Spleen	Spleen
14	chr7:99870600-99926200	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr7:99870600-99932800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr7:99870800-99904600	Weak transcription	Dnd41	blood
17	chr7:99871000-99917000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr7:99871000-99923000	Weak transcription	Brain Germinal Matrix	brain
19	chr7:99874400-99932800	Weak transcription	Brain Angular Gyrus	brain
20	chr7:99880400-99917800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr7:99882000-99903000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr7:99882200-99897200	Weak transcription	Primary T cells from cord blood	blood
23	chr7:99884400-99916000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:99886800-99901600	Weak transcription	Fetal Stomach	stomach
25	chr7:99887400-99932800	Weak transcription	Brain Anterior Caudate	brain
26	chr7:99889400-99915000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:99890200-99914200	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr7:99890400-99901000	Weak transcription	Fetal Thymus	thymus
29	chr7:99890400-99917000	Weak transcription	Fetal Brain Female	brain
30	chr7:99892800-99901800	Weak transcription	Fetal Intestine Small	intestine
31	chr7:99893600-99914200	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr7:99893600-99917000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr7:99893600-99917800	Weak transcription	Lung	lung
34	chr7:99893600-99918000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr7:99895600-99896600	Enhancers	K562	blood
36	chr7:99895600-99897000	Enhancers	HepG2	liver
37	chr7:99895800-99896600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr7:99896400-99917000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr7:99896600-99924600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr7:99896600-99931800	Weak transcription	K562	blood
41	chr7:99897600-99933200	Weak transcription	Pancreas	Pancrea
42	chr7:99898000-99932800	Weak transcription	Brain Substantia Nigra	brain
43	chr7:99899200-99901600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr7:99900200-99902400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr7:99901000-99902400	Enhancers	Primary B cells from peripheral blood	blood
46	chr7:99901000-99902400	Enhancers	Fetal Thymus	thymus
47	chr7:99901200-99902400	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr7:99901200-99923400	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr7:99901600-99901800	Enhancers	Thymus	Thymus
50	chr7:99901600-99902000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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