Tag | Content |
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EnhancerAtlas ID | HS050-10987 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr11:4010370-4011480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HOXA13 | MA0650.2 | chr11:4010928-4010939 | GTTTTATTGGC | - | 6.14 | IRF1 | MA0050.2 | chr11:4011312-4011333 | ATCTACTTTCTCTTTCTGTAG | + | 6.43 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 4010907 | 4011380 | chr11 | 4011216 | 4011355 |
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| Number: 2 | ID | Chromosome | Start | End |
GH11I003989 | chr11 | 4010431 | 4010861 | GH11I003990 | chr11 | 4011221 | 4011370 |
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Enhancer Sequence | TGTATGATGT GTGGTATTAT TCAGACTTGG CTTCCTTCTC TCCTGCCTCA TCAGAGGCTG 60 GACTCTCCTC AGTTTTCTTT TCCCTGTTTA CTGCAGGTAA ATGTTCTTTA GTTTCTTGGT 120 TAGCCACTTC GGCCTGTTTT CCCTTTGCTC CCCTTTTCCC TTTTGTTTGC ACTTGTTTGT 180 CTGAAGATTT ATCCTTTGCT GCTGCCTTTT TCGGCTTCGC TTCCACTTTT GCAGGAGCAG 240 GTTTAGCAGA CAACCGCGCC GATCTCCTCT TGGGCTCTTC CTTGGCGGCC CCTTCCGCGG 300 AGCTGACCTT GCTCTTAGGC ATCCTGGCGG CGTGGAGGGT GCGTGCGGGA TGTCTGTGAG 360 CCGCGGCGCA CCGAGAGCCT TCGCGAAGCT GGGCTGCCTG GTCGCTGCCG CTCCTCCCGC 420 CGCCCGAGCT GCTGAGATCC CCAGAAGGGG CGGTGGGAGA ACCCTGATTT TTACATTTTA 480 AAATAGTTTA GGGGGAAAGC TAAAGAAGAA TTTCAAGATG TGAAATTTAT ATGAAATTGA 540 AATTTCAGTG TCTGTAAAGT TTTATTGGCA TACAGCCACT CTCGTTCATT TACATATTGT 600 CTATTGCTGC TTTTACACAA GAACAGCAGA GTTGTGTAGT TGCGACAGAG ACCATATGGA 660 CCACCAGGCC TAAAATATTT ACTGTCTGAC TCTTTACAGA AAAAGTTTAT CTGGCCTCTA 720 GTCTAACCTA TCAATTTTAA AAAAACAGCT TTTTGGAGAA AGAATTCACA TACCGTGCAA 780 TTCACCCATT TATATACAAT TCAATGGGTT TTAGTATATT CACAGATATG TGCAACCATC 840 ACCTCAGTCA ATTAAAAACA TTTTTGTCAC CTCAAAAAGA AACCACATAC GCATTAGCTA 900 TTGTTCTCTC TCCACATTTC CCCCAGCCCT AAGCAACCAC GAATCTACTT TCTCTTTCTG 960 TAGTTTTGCC TATTACGGAC ATTTCATGTA AATTCAATCA TATAATATGT GGTCTGTTGT 1020 AACTAGCTTT TTTCACTTAG CATGTTTTCA AGGTGCATTC ATGTTGTATC AGTACTGCCT 1080 GTACATGTTC ATGTATATAT ATCTGTACTT 1110
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