Tag | Content |
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EnhancerAtlas ID | HS182-20395 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr7:150694010-150695440 |
Target genes | Number: 19 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYC | MA0147.3 | chr7:150694721-150694733 | AGCCACGTGCCC | + | 6.18 | ZNF263 | MA0528.1 | chr7:150695404-150695425 | CTCTCCTCACCCTCCTCTCCC | - | 6.22 | ZNF263 | MA0528.1 | chr7:150695401-150695422 | TCTCTCTCCTCACCCTCCTCT | - | 7.22 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_14722 | chr7:150693599-150694826 | CD4_Memory_Primary_7pool | SE_54329 | chr7:150693238-150696864 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I150996 | chr7 | 150693489 | 150694621 |
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Enhancer Sequence | CAGGTGCGGC TGGCCAGCGA CTGAGAGACC CGGGCGCTAC CAAAAGGGGA GCGGGGTGGC 60 GGGGCAGTTC CTAAGGCTTC CCGGGGGCTG GGAGGTCCCA AACTGTGGGG GAGATCCTTG 120 CCTTTTCCCT TAGAGACTGG AAAGGTAGGG GGACTGCCCC ACCCTCAGCA CCCAGGGGAA 180 CCTCAGCCCA GTAGTGAAGA CCTGGTTATC AGGCCCTATG GTAGTGCCTT GGCTGGAGGA 240 GGGGAAAGAA GTCTAGACCT GCTGCAGGGG TGAGGAAGTC TAGACCTGCT GCAGGGGTGA 300 GGAAGTCTAG ACCTGCTGCA GGGGTGAGGA AGTCTAGACC TGCTGCGGGG GTGAGGAAGT 360 CTAGACCTGC TGCGGGGGTG AGGACAGCTG AGCGGAGCTT CCCTGGGCGG TGCTGTCAGT 420 AGCAGGAGCA GCCTCCTGGA AAAGCCCTGG CTGCTGCTTC TCCCCCAAGA GAGAAGGCTT 480 CTCCCGCCAG GCCAGTCCAG TGCAGCCCCT CACCCACACC CACTGCTACC CCAGTTCCCC 540 TGCTTCGGCC CGCACCCTCC CTCACACCCC AGCCCACAGA CTCGGGGCTG GCCTTAGTTA 600 CTGGAACGCC TGTGACCACA GCACTAAGAG AAGCAAGCTG CCCCATGGGG GACTTGGTCC 660 CATGGCCTTG GCCTCCTTCA CCATCACTGG CCGCCAAAGA GTTTGAAATA AAGCCACGTG 720 CCCAGTGAAT CCCAAAGGAA CCTCAACTAA AATAAAAACA ATCCTATCTG ACACTTGCCT 780 GACCCTCTAA GTCATTCAAA GCTTTAGCTC AACTTCGATC CATCTGAGCT GCCATAGTGG 840 ACCCCACTCA GAGCTGCGTC CCTCCCTTGA CCCCAGGTTG GTCCCTGCCA CTCCCCTGCC 900 CCTGTCACTG ACACATGTTT CCTCCTCCCT CAGGCAGGAG TGGGACCTCC CAGCCTCCTC 960 CTGGGGCCTC CACTCAGAAT GTCAGGATGA GCAGGGTCCT AGGAGGCCTC TGGTGCAGCC 1020 TTCCCTTCCC ACCATCCATG TGCTCAAAGA GAATCACCCG TCCTTTCTTG AATGCCATGG 1080 ATCATGGGGG ATTTGCTGCC CACACTCCTA GGCGGCCTCT TAGACATCCG TTGGTGCCTA 1140 ACCCAAGCAT CAGTTTGGCA GAGGCCGAGT CCCTCCTCTG TACTGGATAC CAAGTCAGCT 1200 TCCATAGGGA TGGGGAGACA CCTGGCCCAG GGAGGAGATG AGAAGCAGCC CGGATGGTGC 1260 TACATATGTC AGAGAGCAGG GCAGGAAGGG ATCAGTGTGG CTGCCAATGG TCAGGAGGGC 1320 GCCATGGAGT GAACCATGGC CCCTGCCTCC TCACCAGCAG CTCCTCTGGA GCTGATACTC 1380 AAGACCCCCC GTCTCTCTCC TCACCCTCCT CTCCCGCTGC CTCGGCTGGC 1430
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