| Tag | Content |
|---|
EnhancerAtlas ID | HS091-03795 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:205493490-205494260 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:205493599-205493618 | TGGTGCCACCTGCTGGCTT | - | 7.14 | | SREBF1 | MA0595.1 | chr1:205493515-205493525 | GTGGGGTGAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_03335 | chr1:205493184-205494114 | Brain_Angular_Gyrus | | SE_04118 | chr1:205492576-205493978 | Brain_Anterior_Caudate | | SE_04919 | chr1:205468740-205495155 | Brain_Cingulate_Gyrus | | SE_05883 | chr1:205467701-205496371 | Brain_Hippocampus_Middle | | SE_06802 | chr1:205477989-205495317 | Brain_Hippocampus_Middle_150 | | SE_08023 | chr1:205478044-205494873 | Brain_Inferior_Temporal_Lobe |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I205524 | chr1 | 205493521 | 205493670 |
|
Enhancer Sequence | TCCCAAGAGG GTCAGAGGAC ACAAGGTGGG GTGATATGCC CTCCCCAGCA TGGGCATATC 60
AGTCCCAGCT GAGGCCTAGA TGGGATTTCG AGGAAGATTC CTGGGCCTCT GGTGCCACCT 120
GCTGGCTTGA GTGCATTCAA CTAGCTCGTC CTCCTACATC AACATCCATT TCCTAGATGG 180
GTCTCACTTG GGCTGGAATG GGACTCTAAG CCCACAGTGG GTCCCACGGT CTCCACATGG 240
TTAAGATCAA TAGGCCAGCT GGCATGTGCC TTCCAGTCCT AACTGCCTAT CAGAGCTGTT 300
TGGGACATCT TACAAAACAC AGACTCTACC TCCAGACACC TATAGAATCA GCCTCTCCGG 360
CTAGGGGGTC CAGGAATCCG TCTTGTTAAG GGTTGGATAC ACCTGAGCTA GAAGTGCGCT 420
GATGAGAGAC ACAGTCAGAG AGGTGGATTC TGAACTGGAC ACTCAAGGTA CAATGGGAAA 480
AAAGGCAGCA CTCACTCTGG AGGAGCTCGT GGTCTCAGTC GGAGACACAG GTAGTCAAGA 540
TGTGCAACAA TCCCAGGTGC CACAGCTCTG GGCTCTACAC TCTTGGCTGT CCTGGGAGGA 600
AGAAACTCAC ACTTTCACGA GCTCTGTCCT TTATCACAGG GATAAAGGGA AAAGGAGCCC 660
CTTCCACCAT GGAGTCTCAT CCCTTCCCTC CCAGAGGCTG GAGTTGGGGG AGGCGTCATG 720
TCTGTGGAGC TGCTAAGGGC TTCAAGCTCA CGGCATTCTA TGTCTCTCCC 770
|
