Variant report
Variant | nsv607170 |
---|---|
Chromosome Location | chr7:61968118-62404706 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:45)
- LncRNA region (count:4)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:45 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr18:18518513..18519030-chr7:61979393..61979915,2 | MCF-7 | breast: | |
2 | chr10:42527395..42527915-chr7:61970565..61971091,3 | MCF-7 | breast: | |
3 | chr3:64043547..64044153-chr7:61969362..61969878,2 | MCF-7 | breast: | |
4 | chr19:14627777..14629340-chr7:61968008..61969542,2 | MCF-7 | breast: | |
5 | chr20:52370017..52370874-chr7:61969357..61969967,2 | MCF-7 | breast: | |
6 | chr20:3786959..3788753-chr7:61967828..61969450,2 | MCF-7 | breast: | |
7 | chr20:46692208..46692789-chr7:61968943..61969520,2 | MCF-7 | breast: | |
8 | chr10:42526394..42527915-chr7:61967791..61969362,3 | MCF-7 | breast: | |
9 | chr13:53432415..53433397-chr7:61969357..61970027,2 | MCF-7 | breast: | |
10 | chr17:41380367..41382313-chr7:62191292..62192792,2 | MCF-7 | breast: | |
11 | chr17:41398894..41400557-chr7:62191292..62192792,2 | K562 | blood: | |
12 | chr10:42525601..42527915-chr7:61967079..61969278,2 | K562 | blood: | |
13 | chr1:149221735..149223983-chr7:61969300..61970873,2 | K562 | blood: | |
14 | chr10:42526395..42527915-chr7:61967791..61969507,5 | MCF-7 | breast: | |
15 | chr18:33251821..33252438-chr7:61968851..61969524,2 | K562 | blood: | |
16 | chr1:121484723..121485367-chr7:62026258..62026778,2 | MCF-7 | breast: | |
17 | chr17:59328333..59331074-chr7:61967802..61970795,2 | MCF-7 | breast: | |
18 | chr7:62093615..62095373-chr7:62122563..62125212,2 | K562 | blood: | |
19 | chr1:121483889..121484797-chr7:61974740..61975240,2 | MCF-7 | breast: | |
20 | chr10:42525601..42527915-chr7:61967079..61969468,3 | K562 | blood: | |
21 | chr7:61967943..61970858-chr7:75931774..75934475,2 | MCF-7 | breast: | |
22 | chr7:61967856..61970847-chr8:58714316..58715816,2 | K562 | blood: | |
23 | chr10:42527395..42527915-chr7:61968790..61969454,6 | MCF-7 | breast: | |
24 | chr7:61967856..61971070-chr8:58714316..58715816,4 | K562 | blood: | |
25 | chr17:59939771..59941744-chr7:61968022..61970059,2 | MCF-7 | breast: | |
26 | chr16:1429819..1431603-chr7:61967775..61969442,2 | MCF-7 | breast: | |
27 | chr2:230809935..230810929-chr7:61969025..61969969,2 | MCF-7 | breast: | |
28 | chr1:191006072..191007919-chr7:61967833..61970042,2 | MCF-7 | breast: | |
29 | chr17:41380312..41382165-chr7:62191292..62192792,2 | K562 | blood: | |
30 | chr20:49942718..49943230-chr7:61968963..61969517,2 | MCF-7 | breast: | |
31 | chr14:102551841..102553604-chr7:61969473..61971085,2 | MCF-7 | breast: | |
32 | chr11:63950861..63953375-chr7:61969464..61971091,2 | K562 | blood: | |
33 | chr7:62093615..62095373-chr7:62122563..62125212,2 | K562 | blood: | |
34 | chr10:42527415..42527915-chr7:61968777..61969450,2 | MCF-7 | breast: | |
35 | chr7:62284727..62285228-chr9:30620902..30621883,2 | MCF-7 | breast: | |
36 | chr7:61552820..61553340-chr7:62284727..62285248,3 | MCF-7 | breast: | |
37 | chr17:41399589..41402142-chr7:62189772..62191292,2 | K562 | blood: | |
38 | chr4:8654425..8657330-chr7:61967859..61969474,2 | MCF-7 | breast: | |
39 | chr10:42527395..42527914-chr7:61968778..61969295,2 | MCF-7 | breast: | |
40 | chr10:42527395..42527923-chr7:61968860..61969524,4 | MCF-7 | breast: | |
41 | chr4:91025999..91028875-chr7:61969348..61970976,2 | MCF-7 | breast: | |
42 | chr17:73511595..73513321-chr7:61968020..61970850,2 | MCF-7 | breast: | |
43 | chr7:61969210..61969976-chr8:53657642..53658150,2 | MCF-7 | breast: | |
44 | chr20:55824160..55824726-chr7:61968550..61969274,2 | MCF-7 | breast: | |
45 | chr14:29714914..29715705-chr7:61970951..61971586,2 | MCF-7 | breast: |
(count:4 , 50 per page) page:
1
No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-AC006455.1-12 | chr7:61971118-61971191 | NONHSAT120885 |
2 | lnc-AC006455.1-12 | chr7:61969203-61969572 | NONHSAT120885 |
3 | lnc-AC006455.1-12 | chr7:61970441-61970493 | NONHSAT120885 |
4 | lnc-AC006455.1-12 | chr7:61968944-61969128 | NONHSAT120885 |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000177303 | chromatin interactions |
ENSG00000168439 | chromatin interactions |
ENSG00000136492 | chromatin interactions |
ENSG00000132002 | chromatin interactions |
ENSG00000236383 | chromatin interactions |
ENSG00000080824 | chromatin interactions |
ENSG00000182173 | chromatin interactions |
ENSG00000099797 | chromatin interactions |
ENSG00000106211 | chromatin interactions |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs7384762 | chr7:61968118-61968119 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
2 | rs74560338 | chr7:61968119-61968120 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
3 | rs570816815 | chr7:61968121-61968122 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
4 | rs60332391 | chr7:61968127-61968128 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
5 | rs76747588 | chr7:61968128-61968129 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
6 | rs57812761 | chr7:61968134-61968135 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
7 | rs55738787 | chr7:61968141-61968142 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
8 | rs565327610 | chr7:61968148-61968149 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
9 | rs62457254 | chr7:61968156-61968157 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
10 | rs62457255 | chr7:61968157-61968158 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
11 | rs58473337 | chr7:61968158-61968159 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
12 | rs535775344 | chr7:61968161-61968162 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
13 | rs62457257 | chr7:61968162-61968163 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
14 | rs149318733 | chr7:61968163-61968164 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
15 | rs80158223 | chr7:61968164-61968165 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
16 | rs76479099 | chr7:61968166-61968167 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
17 | rs79878263 | chr7:61968170-61968171 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
18 | rs62457258 | chr7:61968174-61968175 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
19 | rs76991680 | chr7:61968184-61968185 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
20 | rs62457259 | chr7:61968188-61968189 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
21 | rs76300450 | chr7:61968191-61968192 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
22 | rs62458760 | chr7:61968196-61968197 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
23 | rs565559761 | chr7:61968199-61968200 | ZNF genes & repeats Weak transcription | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
24 | rs62458761 | chr7:61968201-61968202 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
25 | rs539107041 | chr7:61968203-61968204 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
26 | rs111347437 | chr7:61968207-61968208 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
27 | rs77817295 | chr7:61968208-61968209 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
28 | rs78920461 | chr7:61968209-61968210 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
29 | rs557435168 | chr7:61968213-61968214 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
30 | rs61692580 | chr7:61968221-61968222 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
31 | rs576133766 | chr7:61968235-61968236 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
32 | rs78586838 | chr7:61968240-61968241 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
33 | rs374001014 | chr7:61968245-61968246 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
34 | rs149893410 | chr7:61968252-61968253 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
35 | rs200387084 | chr7:61968254-61968255 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
36 | rs77570877 | chr7:61968264-61968265 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
37 | rs75553298 | chr7:61968266-61968267 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
38 | rs555379141 | chr7:61968269-61968270 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
39 | rs575012529 | chr7:61968271-61968272 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
40 | rs28893873 | chr7:61968272-61968273 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
41 | rs542564306 | chr7:61968278-61968279 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
42 | rs560636043 | chr7:61968281-61968282 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
43 | rs147586899 | chr7:61968283-61968284 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
44 | rs112626453 | chr7:61968291-61968292 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
45 | rs199702637 | chr7:61968297-61968298 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
46 | rs58990413 | chr7:61968299-61968300 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
47 | rs377727986 | chr7:61968304-61968305 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
48 | rs60755807 | chr7:61968305-61968306 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
49 | rs527896058 | chr7:61968308-61968309 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
50 | rs112045180 | chr7:61968309-61968310 | ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS | Chromatin interactive region | 6 gene(s) | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Wilms tumour | 21544195 | CNVD |
Medulloblastoma | 21979893 | CNVD |
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 |
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 |
Follicular lymphoma | 20505157 | CNVD |
Biliary cancer | 19435499 | CNVD |
Williams-beuren syndrome | 22470819 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Multiple myeloma | 16461302 | CNVD |
Glioblastoma multiforme | 21750150 | CNVD |
Cancer | 21183584 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Non-small cell lung cancer | 21829676 | CNVD |
Gastric cancer | 24379144 | CNVD |
Glioblastoma multiforme | 17002787 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
T-cell prolymphocytic leukemia | 17713554 | CNVD |
Lissencephaly | 21572526 | CNVD |
Breast cancer | 17603634 | CNVD |
Liposarcoma | 21253554 | CNVD |
Breast cancer | 16397240 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Hodgkin''s lymphoma | 18641027 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Lung cancer | 18438408 | 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 |
Glioblastoma | 21080181 | 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 |
Non-syndromic sensorineural hearing loss | 17122850 | CNVD |
Breast cancer | 21990379 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Schizophrenia | 21399695 | CNVD |
Malignant fibrous histiocytomas | 21085701 | CNVD |
Astrocytoma | 22246337 | CNVD |
Renal cell carcinoma | 18592004 | CNVD |
Bipolar disorder | 19214233 | CNVD |
Acute promyelocytic leukemia | 19109227 | CNVD |
Non-syndromic sensorineural hearing loss | 21293372 | CNVD |
Breast cancer | 21364760 | CNVD |
early-passage human iPS cells | 21368824 | CNVD |
Acute monocytic leukemia | 16498392 | CNVD |
Prostate cancer | 16461572 | CNVD |
Salivary gland tumor | 18059337 | CNVD |
Schizophrenia | 23813976 | CNVD |
Multiple myeloma | 17550852 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
Non-syndromic sensorineural hearing loss | 22037309 | CNVD |
Congenital anomalies of the kidney and urinary tract | 18316590 | CNVD |
Schizophrenia | 20967226 | CNVD |
Breast cancer | 22522925 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:61967200-61968800 | Weak transcription | Lung | lung |
2 | chr7:61967200-61968800 | ZNF genes & repeats | Pancreas | Pancrea |
3 | chr7:61967200-61969600 | ZNF genes & repeats | Primary neutrophils fromperipheralblood | blood |
4 | chr7:61967200-61969600 | ZNF genes & repeats | Primary T helper cells PMA-I stimulated | -- |
5 | chr7:61967200-61969600 | ZNF genes & repeats | Colonic Mucosa | Colon |
6 | chr7:61967200-61969600 | ZNF genes & repeats | Duodenum Mucosa | Duodenum |
7 | chr7:61967200-61969600 | ZNF genes & repeats | Stomach Mucosa | stomach |
8 | chr7:61967200-61969800 | ZNF genes & repeats | Sigmoid Colon | Sigmoid Colon |
9 | chr7:61967200-61969800 | ZNF genes & repeats | Spleen | Spleen |
10 | chr7:61967200-61969800 | ZNF genes & repeats | Hela-S3 | cervix |
11 | chr7:61967200-61969800 | ZNF genes & repeats | HUVEC | blood vessel |
12 | chr7:61967200-61970000 | ZNF genes & repeats | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
13 | chr7:61967200-61970000 | ZNF genes & repeats | Adipose Nuclei | Adipose |
14 | chr7:61967200-61970000 | ZNF genes & repeats | Liver | Liver |
15 | chr7:61967200-61970200 | ZNF genes & repeats | Monocytes-CD14+_RO01746 | blood |
16 | chr7:61967200-61971600 | ZNF genes & repeats | Fetal Intestine Large | intestine |
17 | chr7:61967200-61971800 | ZNF genes & repeats | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
18 | chr7:61967200-61972200 | ZNF genes & repeats | Colon Smooth Muscle | Colon |
19 | chr7:61967200-61973600 | ZNF genes & repeats | Primary T cells from cord blood | blood |
20 | chr7:61967200-61973600 | ZNF genes & repeats | Primary T cells effector/memory enriched fromperipheralblood | blood |
21 | chr7:61967200-61973600 | ZNF genes & repeats | Gastric | stomach |
22 | chr7:61967200-61973600 | ZNF genes & repeats | Left Ventricle | heart |
23 | chr7:61967200-61973800 | ZNF genes & repeats | H1 Cell Line | embryonic stem cell |
24 | chr7:61967200-61973800 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
25 | chr7:61967200-61973800 | ZNF genes & repeats | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
26 | chr7:61967200-61973800 | ZNF genes & repeats | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
27 | chr7:61967200-61973800 | ZNF genes & repeats | HUES48 Cell Line | embryonic stem cell |
28 | chr7:61967200-61973800 | ZNF genes & repeats | HUES6 Cell Line | embryonic stem cell |
29 | chr7:61967200-61973800 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |
30 | chr7:61967200-61973800 | ZNF genes & repeats | iPS-18 Cell Line | embryonic stem cell |
31 | chr7:61967200-61973800 | ZNF genes & repeats | iPS-20b Cell Line | embryonic stem cell |
32 | chr7:61967200-61973800 | ZNF genes & repeats | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
33 | chr7:61967200-61973800 | ZNF genes & repeats | Primary hematopoietic stem cells | blood |
34 | chr7:61967200-61973800 | ZNF genes & repeats | Primary hematopoietic stem cells short term culture | blood |
35 | chr7:61967200-61973800 | ZNF genes & repeats | Primary T regulatory cells fromperipheralblood | blood |
36 | chr7:61967200-61973800 | ZNF genes & repeats | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
37 | chr7:61967200-61973800 | ZNF genes & repeats | Duodenum Smooth Muscle | Duodenum |
38 | chr7:61967200-61973800 | ZNF genes & repeats | HMEC | breast |
39 | chr7:61967200-61976600 | ZNF genes & repeats | Primary B cells from cord blood | blood |
40 | chr7:61967400-61968800 | ZNF genes & repeats | Dnd41 | blood |
41 | chr7:61967400-61969600 | ZNF genes & repeats | Placenta Amnion | Placenta Amnion |
42 | chr7:61967400-61970000 | ZNF genes & repeats | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
43 | chr7:61967400-61971400 | ZNF genes & repeats | Primary T cells fromperipheralblood | blood |
44 | chr7:61967400-61973800 | ZNF genes & repeats | Fetal Stomach | stomach |
45 | chr7:61967600-61968200 | Weak transcription | Right Atrium | heart |
46 | chr7:61967600-61968200 | Weak transcription | NHEK | skin |
47 | chr7:61967600-61968800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
48 | chr7:61967600-61968800 | Weak transcription | Fetal Brain Female | brain |
49 | chr7:61967600-61968800 | Weak transcription | Right Ventricle | heart |
50 | chr7:61967600-61969200 | Weak transcription | NHDF-Ad | bronchial |