Tag | Content |
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EnhancerAtlas ID | HS180-21556 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr17:70497700-70499480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr17:70498944-70498965 | GGAGGAGGAGGCTGGGAGGGA | + | 6.86 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_23138 | chr17:70497336-70499532 | Colon_Crypt_1 | SE_23878 | chr17:70497510-70499239 | Colon_Crypt_2 | SE_27375 | chr17:70497516-70499407 | Esophagus | SE_27674 | chr17:70497675-70498765 | Fetal_Intestine | SE_28662 | chr17:70497435-70498801 | Fetal_Intestine_Large | SE_31559 | chr17:70497243-70500103 | Gastric | SE_33632 | chr17:70497070-70499626 | H2171 | SE_47128 | chr17:70496641-70501764 | Panc1 | SE_47739 | chr17:70497293-70499529 | Pancreas | SE_50247 | chr17:70497339-70499493 | Sigmoid_Colon | SE_52735 | chr17:70497690-70499276 | Small_Intestine | SE_65456 | chr17:70497086-70499432 | Pancreatic_islets |
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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 |
GH17I072501 | chr17 | 70497285 | 70499996 |
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Enhancer Sequence | CAGGAGAACA GCCCTTACGC AAACTTCCAG GGCGGTCTGG CCTCTGCTTA CCTCCTCAAC 60 CCTGGAACTA TTCCACAGAG TGCAAGTTTC ATCGCAGGCC CCTAGGGAAT CCAGACCCTT 120 CTAGAGATCT ATCCCTGGGT CCCTACCCCA ACCCTTCTCT CTGTCTTCCA CGAGCCACAC 180 CCCTCCCTGC CCTTGCCTCA GAAAGCCCTC ATTCTGAAGG TCAGGTCCAC TTAGCGGTCA 240 GCCTCGCTCC CCAGCCGCCC AAGGTGGCTG GGATCAGTGG TGAGGAAGGG AGAGGAGGTG 300 AAAGGAGGAT AAGCAGAGAG CAAGGAGGCC CCGTGAGGTC TTGTGACCGA CTGGGCCTCC 360 TGGTGCCGCC GAGGTGGCAG TGCCAAAGCG CAGTGCTGGA ATACTTGGCC TGTCTCCGGA 420 GCAAACACCC AATCCAAACA GGCCCTAGTG TGTCTCCGAA CAGACTGTGT AAATAACGGG 480 GGGAGGAAAA AAAAACCCCA ACTGGCCACA GATCCCGCTT TCAAACACAT TGAAACAAAA 540 TAATCCCTCT CTCCCTCACT CGCTCACTCC CCACTGCTTG CTCTTTTTTT TTTTTTTTTT 600 TTTAAATTTC CACCGGTGCC GAGGCCTCAG TGGAGCCTGG CTGGCGGCTT GTTAGAGCCT 660 GCAGCCTACC TGTCCTGCAT AGGAATGAAG CCGGGAGGAG TTACATGATA TGCCCTCGTT 720 GCAGGCCGGG GACACAGCTA CCGCATTCAG AGACCAGGAA ACAGAGCAAA AGCTGTTCTC 780 AGAGTGCGGC TGAGCGAGGA GCTACAGGGG AATGGAGGGG GCCAAGCTGC ATGGAAGATT 840 GTCCCATTAA CCTGGCTTTT TACCAGGGTG GTCCTCTCCC TAACCCCTAA GAATCACACC 900 CTGCATCCAA ACGGCAGCAA CCCCAGAAAA CGGGCTAAGA ACTCCCCCGA ACAGAGCTAG 960 ATCTAGAAAG CCCAGCACAG GGAGCTGAGC CTGAGCAGCC TCTCTCCAAG GGTGGCTCTG 1020 AACTCCACAT GTGTGTACAG ACAAGGGGGC GACTGGCATG TGGTTTGTTT CTGGTCTTGT 1080 AGTCGGTTTG GAATTTTCTA AGTCAGGGTG GGGTGGGGGG ACTGTGCACG AGTCATGTGC 1140 AGACTGGAAC CCATCTCCCC CTCGGTCTGC AAGTTAAAAC AATTGGGTTG TCCTTCTCAG 1200 CATCTGCCAA TGTCTCTTAC TCAATCTTGG ATCAAAAGGG CGTTGGAGGA GGAGGCTGGG 1260 AGGGAAATCC AGACAGTTCT CCGCCTCTGA CATCAGGTCC AGCTGTTAGC ATCGTGCTGT 1320 GGGTCCCTGA ACAAGAAGCA AAGTCAGGAC TGGTTTGGCC AGGTAGGTGA GGATCCAGTG 1380 TTGGGTGATT CTGATCCATG CAGCCCTTAG AGGCGACACA GACGTGAACT GGACATTCTA 1440 GGAAGAAAGA GCCGACTGCC GGGTGACCTG TCTAGTTCAC ATCCACTCAC CATTTCCCTC 1500 CTCGTTCCTA TTCTTAGAAA TAAGACTCTG ACGCTCTCTT TTATACAGGC TAGTCCCCTA 1560 TAGGCATGTC ATGGTGATTA TTTGCAATCC TCCTGACTTT CCTAAGAAGA GATCAGACTT 1620 AGCAGGGTTA GTCCTCATAG CCCGAGGCTG GACAGGAAGA GAACTCCATA TCCTATGTCC 1680 AAGAATATCA TCAAATCCTT ATGAAGCACC AGTTGTTGTG ACGCAATTTT AAAAGACTGG 1740 TTCAAAGTGC CTGTCTGAGA CTAAGCAGAT CTGTGGGTCG 1780
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