Tag | Content |
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EnhancerAtlas ID | HS110-03772 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr4:113033840-113035230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr4:113034722-113034733 | ACAGATAAGAA | - | 6.14 | Gata1 | MA0035.3 | chr4:113034722-113034733 | ACAGATAAGAA | - | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 113033871 | 113034904 | chr4 | 113034135 | 113034634 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I112112 | chr4 | 113033251 | 113035216 |
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Enhancer Sequence | GGAGGCTTGG GGCTAGAACA GCAGAGTTCC TATGGGAAGT AGGGGTGAGG CTCAAGCTGA 60 AATCAGGGCC TAGTTGAAAG ACTGTACAGT CTGTTTGTTT ATGAAGCAGC TGGAAGTCTA 120 GGCCCCTTTC CCACTTCACC TCACCCATCA AGGACCAGAA ATTCACTCAG AGAAACCCTG 180 AACTCCTGAA ACCAAACATA GTGTGGCAGA TGGAAGACTG AAAATAGGGG GTGGGGGATT 240 AAGTGAAAAT CTGGATGCTG AAACTAAGAC TTTCAGCTGC TTTTTCTACT CTACATTCAG 300 AACAATAGCA GCCAGACTTA CACACCGACT CTGTCACATT TGCCCCTCCA TCCCCAATTC 360 ATATTTAAGT ACATTGAAAG GATTCTTGAG AAGCGTGTGA CAGAGATATC ATAAGATCTG 420 GAAAATCAGC AAGAAGATCT TAGCAAACTT GGCAAATGAA AAGGGAGAAT TATTAACTGC 480 AGGGAAAAGT ATTATATGAG AAAGAGGTGT GGTGTAGTGC ACAACATGGC TAAACATTGC 540 GTAACATTTG CACAGTCATG ATAATGTAAA CACTGAGTAT TGGTTTAGCC AAAAATGCTA 600 ATGTAACTAC ATCAGGGGAT AGGGGAAGGA AACTGATGGA ACACAGGAGT TTTCTAGGTA 660 TTATTGTTTG GCCTTCAACA TACATTCGCA CTCTTTCCAC ATACCCCCTT AATTACAAAG 720 GCTGGGAAGC TAAAAATGAC CACATTTCCC AAAAGGTCCT GCAGCTACAG TTCTGGACAC 780 AATTTAAGTT CTCTCATAAG ATGCACTCAT TTGAGATTTG GAAGGCAGAA GTGAGGCAAA 840 GGCCATTTTC TTGTGACTGA GGCAGCTGGT AAACAAGATT AGACAGATAA GAATGTTTGC 900 AGTAGGCCAG GCACAGTGGC TCACGCCTGT AATCCCAGCA CTTTGAGAGG CTGAGGCAGA 960 TGGATCACCT GAGCTCAGGA GTTTGAGACC AGCTTGTCTA ACTTGATGAA ACCCCGTCTC 1020 TACTACTAAA AATACAAAAT TAGCCAGTCA TGGTGGTAGG TGCCTGTAAT CCCATCTACT 1080 CAGGAGGCTG AAGCAGGAGA ATCGCTTGAA CCCAGGAGGT GGAGGTTGCA CTCCATTCTG 1140 GGTGGCAGAG CAAGATGCAG TCTTTAAAAA AAAAAAAGAA GAAGAAGAAG AAGAATGTTT 1200 GCAGTAGGCA GACTTCACAT CCTAATGTGT CTTCATGGAT GTGGGGCATT AGCAGAGGTG 1260 ACAACAGCAG CCACCTGACC TCTGTATCAA CCCTACTCTA CATGGTATGC CACTGAACCC 1320 AATAGTCCTG CAACAGCCTT TGCCTCCCAC TCAGTTTTTC CCTGCCCCAT CCCCTACTCC 1380 CAACAATTTA 1390
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