Tag | Content |
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EnhancerAtlas ID | HS048-03480 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:224393040-224394390 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:224393337-224393357 | CCCCCCCCCAACCCCAACAC | + | 6.6 | Zfx | MA0146.2 | chr1:224393078-224393092 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65181 | chr1:224391966-224393881 | NHEK |
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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 |
GH01I224202 | chr1 | 224390586 | 224394441 |
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Enhancer Sequence | TAGCCGGGAT GGTCTCGATC TCCTGACCTC GTGATCCGCC CGCCTCGGCC TCCCAAAGTG 60 CTGGGATTAC AGGCGTGAGC CACCGCGCCC GGCCGACTTG GCTTTTTAAA TTGCCTTCTA 120 TGAATATATA TTTGTCCTAA GACTGGACTG GCCACATGAA ATCAGGTTTT CAAAACGGAA 180 CTGCCTGTGA GGATGTGTGA GTGTGGATGT CAGGTGGCAA GGGGCTGAGA AGGAAAGTGC 240 AAGGGGGCCT CCCATCCCAC ATGACTCACA CGTTGCTCAC ATACACACAC CCAGCCCCCC 300 CCCCCCAACC CCAACACACA CACGCAGGGC TGTAAACCAT ATGATTAGGC TCCTGCCTGA 360 CTCTCCCAGG CCATCTCTCC CTGTGGTCCA GCCACCATGG GCTGCTTTCT GCTCCAAACA 420 CACTCAGGAT TGCTGTGTCC CAGGGCCTGC TTGGTGTCCT CTGCGTAGAC ACTAGACCAG 480 AGCTCACAGA GCCACCTCCC TCTCAATAAT CAGCTCTCAG CTCAAATGCC ACCTCTTTAA 540 AGAAGACTTC CTTAGAAACG GCCTGATTTC TAGTTTCACC AAAAACTGAC CCTGAGATGA 600 GAATTTGGGT ATATGGCTTA TTTGGAAGGT GATCCTGAAA TGAGTGAGAA AAGGAAATCC 660 AAAAAAGCAG GCCAGTAAAG CGTGTGTCAC TTAAGGAGCA GGTAACCACT GTAGGCAACT 720 GGAGCTCATT CCCCAGGACT CCTGAGAGCT CTCGCAATGT CCCACCAATG GTTACAGAGG 780 TGTTTGCCTT GGAGTAATTC ATTAAGCTGC ACGTTTGCTC TGTGTATTTT TCTGTATCTG 840 GATTTTACAA TACAAGATTT TTTGTTTTGT GTTTTGTGTT TTTTGAGACA GAGTCTCGCT 900 CCGTCACCCA GGCTGGAGTG CAATGGTACG ATCTCGGCTC ACTGCAACCT CCGCCTCCCA 960 GGTTCCAGCG ATTCTCCTGC CTCAGCCTCC TGAGTAGCTG GGATTACAGG CACCTGCCAC 1020 CATGCCTGGC TAATTCTGGT ATTTTTTTAG TAGAGATGGG GTTTTACCAT GTTGGCCAGG 1080 CTGGTCTCAA ACTCCCAACC CCAGGTGATC CGCCTGTCTT GGCCTCCCAA AGGACTGGGA 1140 TTACAGGTGA GAGCCACCAT GCCTGGCCAT TTTTTGTTTT TTGAGAGAGT CTCACTCTGT 1200 CACCCAGGCT GGTGTGCAAT AGCGTAATCA CTAAGTGCAG CCTTGACCTC CCAGGCTCCA 1260 ATGATCCTCC TACCTCAGCT GATACTACAG GCATATGCCA CTGTGAAAGA AAAATAAACC 1320 TTGGAGCCCT AAAAGCACTA AGCTAAAGGG 1350
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