Variant report

Variant	nsv482714
Chromosome Location	chr7:102296392-102454063
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2567)
CpG islands
(count:1714)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2567 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102452449-102452773	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102339769-102340073	K562	blood:	n/a	n/a
3	ARID3A	chr7:102386072-102386189	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:102389084-102389458	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:102386048-102386259	K562	blood:	n/a	n/a
6	ATF1	chr7:102389031-102389497	K562	blood:	n/a	n/a
7	ATF1	chr7:102339824-102340183	K562	blood:	n/a	n/a
8	ATF2	chr7:102353660-102354116	GM12878	blood:	n/a	n/a
9	ATF2	chr7:102389081-102389544	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr7:102389108-102389584	GM12878	blood:	n/a	n/a
11	ATF2	chr7:102353714-102354151	GM12878	blood:	n/a	n/a
12	ATF3	chr7:102312099-102312242	K562	blood:	n/a	chr7:102312144-102312152
13	ATF3	chr7:102312022-102312401	A549	lung:	n/a	chr7:102312144-102312152
14	BATF	chr7:102352581-102352892	GM12878	blood:	n/a	n/a
15	BATF	chr7:102356182-102356563	GM12878	blood:	n/a	n/a
16	BATF	chr7:102410945-102411178	GM12878	blood:	n/a	n/a
17	BATF	chr7:102313151-102313476	GM12878	blood:	n/a	n/a
18	BATF	chr7:102310144-102310402	GM12878	blood:	n/a	n/a
19	BATF	chr7:102310540-102311004	GM12878	blood:	n/a	n/a
20	BATF	chr7:102306478-102306740	GM12878	blood:	n/a	n/a
21	BATF	chr7:102330287-102330744	GM12878	blood:	n/a	n/a
22	BATF	chr7:102305017-102305524	GM12878	blood:	n/a	n/a
23	BATF	chr7:102311459-102312701	GM12878	blood:	n/a	n/a
24	BATF	chr7:102312293-102312492	GM12878	blood:	n/a	n/a
25	BATF	chr7:102329824-102330101	GM12878	blood:	n/a	n/a
26	BATF	chr7:102400501-102400644	GM12878	blood:	n/a	n/a
27	BATF	chr7:102313180-102313439	GM12878	blood:	n/a	n/a
28	BATF	chr7:102355431-102355796	GM12878	blood:	n/a	n/a
29	BATF	chr7:102352630-102352884	GM12878	blood:	n/a	n/a
30	BATF	chr7:102353557-102354555	GM12878	blood:	n/a	n/a
31	BATF	chr7:102400487-102400681	GM12878	blood:	n/a	n/a
32	BATF	chr7:102353721-102354553	GM12878	blood:	n/a	n/a
33	BATF	chr7:102356109-102356632	GM12878	blood:	n/a	n/a
34	BATF	chr7:102355536-102355847	GM12878	blood:	n/a	n/a
35	BATF	chr7:102382888-102383234	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:102356208-102356576	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:102330097-102330855	GM12878	blood:	n/a	chr7:102330751-102330764
38	BCL11A	chr7:102305225-102305593	GM12878	blood:	n/a	chr7:102305424-102305433
39	BCL11A	chr7:102313169-102313449	GM12878	blood:	n/a	n/a
40	BCL11A	chr7:102353677-102354018	GM12878	blood:	n/a	n/a
41	BCL11A	chr7:102296701-102296848	GM12878	blood:	n/a	n/a
42	BCL11A	chr7:102382918-102383177	GM12878	blood:	n/a	n/a
43	BCL11A	chr7:102352667-102352857	GM12878	blood:	n/a	n/a
44	BCL11A	chr7:102311468-102312674	GM12878	blood:	n/a	chr7:102312277-102312290
45	BCL11A	chr7:102311440-102312266	GM12878	blood:	n/a	n/a
46	BCL11A	chr7:102310539-102310728	GM12878	blood:	n/a	n/a
47	BCL11A	chr7:102301177-102301426	GM12878	blood:	n/a	n/a
48	BCL11A	chr7:102298598-102298785	GM12878	blood:	n/a	n/a
49	BCL11A	chr7:102410971-102411150	GM12878	blood:	n/a	n/a
50	BCL11A	chr7:102352587-102352904	GM12878	blood:	n/a	n/a

(count:1714 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102389275-102389325	AoSMC	blood vessel:	n/a
2	chr7:102389191-102389241	HAEpiC	amniotic membrane:	n/a
3	chr7:102385712-102385762	Hela-S3	cervix:	n/a
4	chr7:102329146-102329196	HMEC	breast:	n/a
5	chr7:102313412-102313462	AoSMC	blood vessel:	n/a
6	chr7:102390529-102390579	AoSMC	blood vessel:	n/a
7	chr7:102389275-102389325	AoSMC	blood vessel:	n/a
8	chr7:102389191-102389241	HAEpiC	amniotic membrane:	n/a
9	chr7:102385712-102385762	Hela-S3	cervix:	n/a
10	chr7:102329146-102329196	HMEC	breast:	n/a
11	chr7:102313412-102313462	AoSMC	blood vessel:	n/a
12	chr7:102390529-102390579	AoSMC	blood vessel:	n/a
13	chr7:102311965-102312015	BE2_C	brain:	n/a
14	chr7:102388500-102388550	HEEpiC	esophagus:	n/a
15	chr7:102389315-102389365	ECC-1	luminal epithelium:	n/a
16	chr7:102388500-102388550	BJ	skin:	n/a
17	chr7:102389191-102389241	Jurkat	blood:	n/a
18	chr7:102312200-102312250	SK-N-SH_RA	brain:	n/a
19	chr7:102312200-102312250	HCT-116	colon:	n/a
20	chr7:102332458-102332508	RPTEC	kidney:	n/a
21	chr7:102389790-102389840	HCF	heart:	n/a
22	chr7:102389790-102389840	ECC-1	luminal epithelium:	n/a
23	chr7:102389790-102389840	PANC-1	pancreas:	n/a
24	chr7:102313412-102313462	AG09319	gingival:	n/a
25	chr7:102385712-102385762	SK-N-SH	brain:	n/a
26	chr7:102311965-102312015	SK-N-MC	brain:	n/a
27	chr7:102330635-102330685	A549	lung:	n/a
28	chr7:102453328-102453378	Caco-2	colon:	n/a
29	chr7:102389392-102389442	HL-60	blood:	n/a
30	chr7:102313389-102313439	ProgFib	skin:	n/a
31	chr7:102332458-102332508	HEEpiC	esophagus:	n/a
32	chr7:102327236-102327286	Hela-S3	cervix:	n/a
33	chr7:102327236-102327286	ECC-1	luminal epithelium:	n/a
34	chr7:102312331-102312381	H1-hESC	embryonic stem cell:	embryo
35	chr7:102388500-102388550	GM12892	blood:	n/a
36	chr7:102389392-102389442	PFSK-1	brain:	n/a
37	chr7:102389790-102389840	HAEpiC	amniotic membrane:	n/a
38	chr7:102308061-102308111	U87	brain:	n/a
39	chr7:102312200-102312250	PrEC	prostate:	n/a
40	chr7:102389239-102389289	AG10803	skin:	n/a
41	chr7:102389892-102389942	GM12891	blood:	n/a
42	chr7:102332458-102332508	GM12878	blood:	n/a
43	chr7:102389239-102389289	NHDF-neo	bronchial:	n/a
44	chr7:102389481-102389531	HRPEpiC	eye:	n/a
45	chr7:102312318-102312368	HepG2	liver:	n/a
46	chr7:102389892-102389942	GM12892	blood:	n/a
47	chr7:102389481-102389531	MCF10A-Er-Src	breast:	n/a
48	chr7:102389275-102389325	HEEpiC	esophagus:	n/a
49	chr7:102313412-102313462	GM12891	blood:	n/a
50	chr7:102389327-102389377	T-47D	breast:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:102452440..102454909-chr7:102615064..102617723,2	K562	blood:
2	chr7:76751236..76751872-chr7:102389110..102389768,2	MCF-7	breast:
3	chr7:102451931..102453738-chr7:102614138..102615717,2	K562	blood:
4	chr7:102450714..102452892-chr7:102454122..102456841,2	K562	blood:
5	chr7:102430529..102431497-chr7:102702527..102703245,2	K562	blood:
6	chr7:102389047..102390959-chr7:102788572..102791008,2	K562	blood:
7	chr7:102387955..102390990-chr7:102714406..102717094,4	MCF-7	breast:
8	chr7:102445308..102447740-chr7:102490751..102492572,2	K562	blood:
9	chr7:102446461..102450682-chr7:102452402..102456233,5	K562	blood:
10	chr7:102446461..102450682-chr7:102452402..102456233,5	K562	blood:
11	chr7:76750772..76751740-chr7:102389401..102390157,2	HCT-116	colon:
12	chr7:102388357..102390801-chr7:102713734..102717426,3	K562	blood:
13	chr7:102449182..102452214-chr7:102453198..102455672,3	K562	blood:
14	chr7:76751236..76752770-chr7:102389322..102390934,2	MCF-7	breast:
15	chr7:102449182..102452214-chr7:102453198..102455672,3	K562	blood:
16	chr7:102389494..102391981-chr7:102714130..102716680,2	MCF-7	breast:
17	chr7:102396782..102398459-chr7:102714684..102716364,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC105052.1-2	chr7:102453685-102453978	NONHSAT122523

No data

Variant related genes	Relation type
ENSG00000228049	TF binding region
POLR2J2	TF binding region
ENSG00000213385	TF binding region
RASA4DP	TF binding region
FAM185A	TF binding region
ENSG00000228049	CpG island
POLR2J2	CpG island
ENSG00000213385	CpG island
RASA4DP	CpG island
FAM185A	CpG island
ENSG00000170632	chromatin interactions
ENSG00000135205	chromatin interactions
ENSG00000214439	chromatin interactions
ENSG00000161040	chromatin interactions
ENSG00000161048	chromatin interactions

Extended variants
information (count: 3230 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:3230 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201615918	chr7:102301602-102301603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs199737758	chr7:102301610-102301611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs199680291	chr7:102301613-102301614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113448155	chr7:102302067-102302068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111757010	chr7:102302118-102302119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545364187	chr7:102302178-102302179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560185837	chr7:102302259-102302260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527509585	chr7:102302263-102302264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574534777	chr7:102302347-102302348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377325724	chr7:102302368-102302369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs62483487	chr7:102302436-102302437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112760544	chr7:102302504-102302505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548890138	chr7:102302536-102302537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562227206	chr7:102302565-102302566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529301390	chr7:102302566-102302567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550569475	chr7:102302572-102302573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200276257	chr7:102302715-102302716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112209185	chr7:102302924-102302925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111666395	chr7:102303235-102303236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201109928	chr7:102303300-102303301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369918636	chr7:102303313-102303314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565058555	chr7:102303653-102303654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539444073	chr7:102303677-102303678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552077686	chr7:102303762-102303763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567035292	chr7:102303875-102303876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377198453	chr7:102303914-102303915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs58764317	chr7:102303971-102303972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534417630	chr7:102304009-102304010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374309489	chr7:102304017-102304018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111320873	chr7:102304028-102304029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370893172	chr7:102304056-102304057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112270281	chr7:102304158-102304159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555650140	chr7:102304211-102304212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150813249	chr7:102304235-102304236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573786069	chr7:102304236-102304237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537902607	chr7:102304252-102304253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556286007	chr7:102304279-102304280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373600637	chr7:102304307-102304308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577761092	chr7:102304350-102304351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545000736	chr7:102304351-102304352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376561589	chr7:102304396-102304397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs28501471	chr7:102304461-102304462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560432492	chr7:102304500-102304501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370659490	chr7:102304510-102304511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572213540	chr7:102304658-102304659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542829985	chr7:102304765-102304766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373741268	chr7:102305311-102305312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560878717	chr7:102305323-102305324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531392069	chr7:102305381-102305382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367575249	chr7:102305396-102305397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:1175 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102301600-102310200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:102303400-102305400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr7:102303600-102305400	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr7:102303600-102305400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr7:102303600-102311800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr7:102303800-102305400	Weak transcription	Liver	Liver
7	chr7:102303800-102305400	Weak transcription	Brain Anterior Caudate	brain
8	chr7:102303800-102305400	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr7:102303800-102308200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:102304000-102311800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr7:102304000-102311800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:102304200-102311800	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr7:102304200-102311800	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr7:102304200-102311800	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr7:102304200-102311800	Weak transcription	Adipose Nuclei	Adipose
16	chr7:102304200-102311800	Weak transcription	Fetal Muscle Leg	muscle
17	chr7:102304200-102311800	Weak transcription	Fetal Stomach	stomach
18	chr7:102304200-102311800	Weak transcription	Thymus	Thymus
19	chr7:102304400-102308400	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr7:102304600-102306800	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr7:102304600-102307000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr7:102305400-102306000	Strong transcription	Primary neutrophils fromperipheralblood	blood
23	chr7:102305400-102306000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr7:102305400-102306000	Strong transcription	Liver	Liver
25	chr7:102305400-102306000	Strong transcription	Brain Anterior Caudate	brain
26	chr7:102305400-102306000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr7:102305400-102306000	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr7:102306000-102308200	Weak transcription	Liver	Liver
29	chr7:102306000-102308400	Weak transcription	Brain Anterior Caudate	brain
30	chr7:102306000-102310000	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr7:102306000-102311800	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr7:102306000-102311800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr7:102306000-102311800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr7:102308200-102308400	Enhancers	Liver	Liver
35	chr7:102308200-102308600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr7:102311800-102312200	Active TSS	H9 Cell Line	embryonic stem cell
37	chr7:102311800-102312200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr7:102311800-102312200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr7:102311800-102312200	Active TSS	HUES6 Cell Line	embryonic stem cell
40	chr7:102311800-102312200	Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr7:102311800-102312200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:102311800-102312200	Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr7:102311800-102312200	Active TSS	Primary B cells from peripheral blood	blood
44	chr7:102311800-102312200	Active TSS	Primary T cells fromperipheralblood	blood
45	chr7:102311800-102312200	Active TSS	Primary hematopoietic stem cells short term culture	blood
46	chr7:102311800-102312200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
47	chr7:102311800-102312200	Active TSS	Primary T helper cells fromperipheralblood	blood
48	chr7:102311800-102312200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
49	chr7:102311800-102312200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
50	chr7:102311800-102312200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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