| Tag | Content |
|---|
EnhancerAtlas ID | HS105-76381 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr8:8939300-8940410 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr8:8939647-8939660 | TTCTAGAACCTTC | + | 7.12 | | SOX10 | MA0442.2 | chr8:8939739-8939750 | TTCTTTGTTTT | - | 6.62 | | TCF7L2 | MA0523.1 | chr8:8940022-8940036 | TTCCTTTGAAGTCC | - | 6.11 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27764 | chr8:8931616-8940631 | Fetal_Intestine | | SE_28660 | chr8:8931504-8940665 | Fetal_Intestine_Large | | SE_38116 | chr8:8937421-8942637 | HUVEC | | SE_56603 | chr8:8938338-8941106 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 8939736 | 8940088 | | chr8 | 8939402 | 8940318 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I009073 | chr8 | 8931488 | 8940483 |
|
Enhancer Sequence | TACAGAGACA AAGGGAGGGG TGCTCCAAAG CCAAGAGAGG GAACCCCCAC AACTCCCATT 60
TCTTATGAAA AATAAGCAAT TTAATTATTC TATGTCTAGA CTTCTCATTA GCCTGCACTG 120
GAAGACCAAA TAAACCCATT AATATTGTTT TTCTGAGCAA AAGTTGTTCT CTCTGTATGA 180
AGAATTCTGC CTTCATCTTA GTCCATCTGG ACCCTGCAGC CAACTTTTAA AGTCACTGTG 240
TCCCCCCACC CCATTAGAAC TCTTAATATT TGTTTAACCT CAGAGTAGAA TGGAAAGCAT 300
GAATGGCAGA TATTTCTTAC GACTCCAGGA AGTGAAGTTT AGTCTCTTTC TAGAACCTTC 360
CATCAGGTGA GGTCCACTAT GAGCCTGGTT TAGAGGGGAA GGAGAATGGA GACCCTCACA 420
ATGTCCTAAG ACTCTTGTTT TCTTTGTTTT TCTTGTTTTC CTCTTACTCC TTTTACCAGA 480
ACTTCTGGCA AGTAACATGT TGACTCATGG TGTTTTATCA CTTCCTTCCT CTGGCTCACG 540
TCCAGTAGAC ATGCTAATGA GTTGCCAAGT CACCAGTAGG CAGGAAAAGA CAGAAGGGCT 600
TCTCTGCCAT GGAAACCTGA TCATCTGGTG TTAATATTCT GAAAATGACA TTCACAAAAT 660
GAGAGTTAAG CTGGATGAGA AGGTATCTCC TGCTTTCTGG CATGAAATCA TTCTTCCTTT 720
GTTTCCTTTG AAGTCCATAT CTGTGTAAAA GATGCAACAG CAGGAATGAT CTGTACTTCT 780
TGGGGGTCTT AATCTCTGCT GTGTTGAAAG GATATTGAAA GAAATGGATG AGGACCTACA 840
TCTGGGCTCC TCATCTTAGA AAGTAGGCAC CTGCTTGGGA ACACTTAGGC AAATGGATTC 900
TCTCCTTCCC CATTTCCCTT CAGGGGCCAG AAGGTCGGAC AGAAAGTCCA CCCTTGAACC 960
TATCTAACGT CTAGGAGAAA GTCTTTCTAG AAACATAGAG AAAGTGAATG ATGAGATGCC 1020
CGAAGAGTCA TAATAGCAAG AGTCCGGTCT AGTCAGTTCA GGGTGAACTA AGACATGGAA 1080
TGCATTGGAG AAAAGTGGGG ATGATGGAAT 1110
|
