| Tag | Content |
|---|
EnhancerAtlas ID | HS101-00890 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:27668640-27670880 |
Target genes | | Number: 30 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr1:27669321-27669332 | CCCAATCCACA | + | 6.14 | | FOXH1 | MA0479.1 | chr1:27669357-27669368 | CCCAATCCACA | + | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27447 | chr1:27665700-27672263 | Esophagus | | SE_34417 | chr1:27666889-27670810 | HCT-116 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGTAACACGT GTCGGTGCCA GGGTCCCCTG CCAGGGTCCA GAGACGCAGG CACTGCCACC 60
TGGTATCCTG AGCACCCTCC AGCACCTTGG GGTTGGGGGA GGTGGGCACA TGTCTGGAAC 120
TGGAACAGCT GGACAGATGG ACAGACCCTC CTCTTGACCA ATGGGTCTGT CCCACCGTGT 180
CAAAACAGCA GAGAAGACCA AACTCCTACC TAACTCTGGT AGGAGATTCT GCCTCTGGTT 240
GGTAGGAGAG GGGACTTCAG GGAGGGGGCA CTGCTGAGGA CGCTGGGCTG ATGCCCATGG 300
CCCAGCTCAG GCAGGCCTGA AGGACAGAAA TAGGCTCAGT TCTGCCGAAC GTCCCCCCGG 360
CCTCCATCCA CACTCAGACA CACACACCTG GTGGCCCCCA AGGCACCAGG GGACACCCCA 420
CAGCACACAG CCCAGTCACA CATACAGCAC AGGAGGAAAT GCACAATGCA TACTGTACAC 480
ACCCCACACG GCGCTGTCAC CTAGAAAGTC ACTGAACACA CCACACAGAC AATATAGTCA 540
CCATGCAGCA TCACACTGCA ACAGGACACA AAGACACACA GCAACTACAC AGCTCACAGA 600
CTCACGCAAC GCAGACATGC CCACCAGACT CGGACCCACA CAGCCACACA ACAGGGCACA 660
GAGAGGGACG TGGGCTCACA CCCCAATCCA CAGGGGAGGC CGAACGTGGG CTCACACCCC 720
AATCCACAGG GGAGGCCGAA CGTGGGCTCA CACGTTGGCC ACAGAAGTCC AGGGAAACTG 780
CTGTTGTGGA GCACACAGGT ATCCACAGAG TGAATGCACA CCGTGCAGCC GTGCTGAGGC 840
CTTCTGCTCC TGAGGGTGTC AAGAGGGATC GCTGGGGCTC GGCCACTGAC TCAGCTGGGA 900
GGGGACAGAG CATAGCAGGC GGCGGACACA AGCCAGGACC TGCCCGCCAA GCTGCCTCCG 960
CCGGTCTCAG CCCCACCTGG AGCCGTGGCA ATGGAAGGGG CGGGGAAGAG AGGAGAGGCC 1020
GCCCAGTGGG CTCAGGACAC AGCCCTGACC AAGTCATGGG CCCCTTGCCA CGTCTACATG 1080
CCCCTCAGCG CTGGGCAAAT GCTTTCTTTC CGGAGTCACT GTGGTACCTG AGCATGGGCT 1140
GCTGCGCTAG CCTAGGCCTC CACCGCCGGG ACCCCAGCCT GGTCTGGGGA GAACTGTGTG 1200
GCCAGAACAG AGGGGCCCTG TGGCTCCAGG CAACAGGGCA GGGCTGGCGG CGGGGGCATC 1260
CCTGGGTTGG AGGCCTCCGT GGGAGTGGGT GCGGCAGTTA CCTCAGGAGA GGAAGTTGGG 1320
GGTGTGGGCT GAGGAGGAGG TTGCCTCAGA CAGGAAGGCC AAGTGGGCCA GGGCAGGGTG 1380
GAGGTGGTGG CAGGAGGGGA CCCAGGCTGT GAGGTTCCTG GTGCGGGGGA GTGAGCAGAT 1440
GTGTGTGTGT GTACGTGTGT GTGTGTGTGT ATCTGTCTGT CTAGGTGGGT GGTTGTATGT 1500
GTGCATTCCC ATGTGTGTGC AGGCATATTT CTGCATTTAA TTAATCAAAC TTTTACCAAC 1560
CATCTGTTGT GTGCAAAGTA ATGGCTTTGA GGGTGACTCC CTCTCCCTGC CTCCAAGGAG 1620
CTCACAACCC AGTTAGCCGG GCAATGTATG TGTGCCAAAG TCTGTATGAT TTTTATGTAC 1680
ATCTTTATCG AGGGACATAT TTGTCCCCAG ACTTGTTCTT GTCTAGGTGA ACCCATCCGG 1740
GTGGGCCTAT CCCCATTGGT GTGCATATGC TGTGTGCAGG TTTTTTTGTT AGTTTTTGTT 1800
TTGAGACGGA GTCTCACTCT TGCCCAGGCT GGAGTGCAGT GGCGCCATCT CAGCTCACTG 1860
CAACCTCCTT CTCTTGGGTT CAAGTGATTC TCCTGCCTCG CTTCCCAAGT AGCTGGAATT 1920
ACAGGCATGT ACCACCATGC CCAGCTAATT GTTCTGTTCT TTTCATTTTT TTTGGAGGAG 1980
TTTCACTCTT TTTGCCCAGG CTGGAGTGCA ATGGTGTGAT CTCGGTTTAC CATAACCTCT 2040
GCCTCCCAGT TTCAAGCAAT TCTCCCACCT CAGCCTCCCG AGTAGCTGGG ATTAAAGGCA 2100
TGCACCACCA TGCCCGGCTA ATTTTGTATT TTTAGTAGAG ACGGGGTTTC TCCGTGTTGG 2160
TCAGGCTGGT CTCAAACTCC TGACCTCAGG TGATCTGCCC GCCTTGGCAT CCCAAAGTGC 2220
TGGGATTACA GGGGTGAGCC 2240
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