Tag | Content |
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EnhancerAtlas ID | HS182-16490 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr3:169762240-169763160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr3:169762886-169762907 | GGAGGAGAATGAAAAGAGGAA | + | 6.19 | ZNF263 | MA0528.1 | chr3:169762565-169762586 | CCCTCTCCCCCATCCTTCTCT | - | 6.41 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28357 | chr3:169761085-169765553 | Fetal_Intestine | SE_29014 | chr3:169760925-169769213 | Fetal_Intestine_Large |
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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 |
GH03I170043 | chr3 | 169761100 | 169768921 |
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Enhancer Sequence | GCTGCCTATT TTCTCACTTA TAAGGAACTT GTTCGCTACC CCCTGCAGTT TGACAAGAAT 60 GGAGTAGGTG TGGGCAGGCC TCAGTAGGGA AAAGGAATGG CTCCAAACTC CCACACCATT 120 GGGTCTTTGT GAGTAGGCAG GTGGGTCTTG TGCACCTTGG CGGTTCCCCA GGGTGTCCTG 180 CAGGGATGGG GCACCAAAAA GGCCTTTAAC CCTTCCCCTT TAAGCAGGGG ACCCATGTGG 240 ATCCTGAAGT TGTGCATCAG CTCACTGTAG CTGCTCTGAG CTGGACCCCA GCCACTCTGA 300 GGGGTTCCTA GGACTTGCAA AGGGCCCCTC TCCCCCATCC TTCTCTGCCT ACCACTCTCC 360 TGCTGATGAC AAGTCCACTT CTATACACTG CTTAGGCACA GCCCCCCAAG AAAGCTCTGC 420 AGGGATGAGG AGCTGAGGCA CCCGCATAGT CCAGCCTTAA GGGGTTTCTG TGATGCAAGT 480 CCAAGGGTGG CTTAATTTCC TTGCCTTGAA ACTTTCGGTT AAGGGTCACG GGGCAAACAT 540 TCTCGCTTCT GTGAATAGCT GGAGTTTCAT GACAGTTGAA GTTTCTCTTT AGATCTTTGT 600 TTCCTTCCCC TGAGTTCTGC ATTTTCTTCC CATGTACGTG TGCCGTGGAG GAGAATGAAA 660 AGAGGAAATG GCACAAAAGT GAACCTTGTT GGGTGGCTTT CAGGAAATGT CAGGTGCTGT 720 TGTGGGCCTT TGTCACTCGA GTTGTCAGTC TAGGTGTGTG TGTAAACGGA CATGGAATAA 780 ACAAGGGCTC CAAGTGGAAC AGCTTGTTTT GGCCAAAAGA AGTGAGTTCA GGCCGAGCAT 840 GGTGGCTCAC ACCTGTAATC CCAGCACTTT GGGAGGCCGA GGTGGGTGGA TAGTGAGGTC 900 AGGAAATCGA GACCATCCTG 920
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