| Tag | Content |
|---|
EnhancerAtlas ID | HS129-27189 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr4:6696930-6698610 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr4:6698591-6698606 | GCTGACCTTGAGCCT | - | 6.9 | | Stat6 | MA0520.1 | chr4:6698282-6698297 | CATTTCCTGAGAACA | + | 7.08 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_32360 | chr4:6693831-6699251 | Gastric |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AATGCGTCAG CCTCGACATC TCAAAGTGCT GTGATTACAG GCGTGAGCCC CGACACCTGG 60
CCTAGTTCTA TTTTCTAAAT GTGAATTCTG TAAAGATATC TTTTAAAAAT AAAGTTCTGT 120
TTTTGGTAGA AAATGTAAAA ATAGATAAAT ATGGAGGGAA GAAATCCCCC CTGGAATACA 180
GACGCTTCCT CTCCCTTCCA GCCTTTTCCC CATATGAACA TTGCTGTGAG TGAGATTTAC 240
ATGCAATGTA ATTTCTTTTT GAGCTTAACA TTACAACATA AATTCTCAAA CTCTGATGTT 300
CATTAAACAC CCCAGCCCCA TCCTGGGAAC TTGGGCTTGG GGCTCGGGGT GTTCTGATAA 360
TGATCAAAGT ATGAGAATTG AACCCATGAG GACTTTGATC CAAGATACTG GGGTGTGGGG 420
AGGGGCAGGC ACAGGTGTCC TGGGAACACA CTTTGAGAAG CAATGGCAAA GCTGGGGGTC 480
CAGCTAATGT GTTACATTAG AATCACCTCG GGGAGGCCCT GGGTGCCCTT CTCAGCCCTC 540
CCTCCGGAGG CTGCTGAAGC CCAGCAAAGC CGGAGTCAGA GAACAATGTC CGCCTGAGGG 600
CAGGGCTGGG CTGGGCTGGC CTTCTGGCCC TATCTGCTCC GTGCCCAACC CAGCGCCCCG 660
CACAGTCGGA GCTTTGTAAA TACGAGGTGA CTGTCTGCCT ACAAACTTTG TAAACATCAC 720
TTGAAATGGC CGCAGGGTAT TGTGACATGG CCATACCACT ATTTGTTTGC TATTGAATTT 780
GTACTTCCCT GCCTTACTTT TGCTATTGCA AACCATGCTG TCACTAAGGT CTTCATGCAC 840
ACAGTTGTGT CTTGGTCAGA TGATATGTTT CTACCAATTT TAATTGTGTT TCTTTCCACC 900
TGGACACACA GCTCTCTGGC CCAGGGCTGG GTCATCAGCA CACCCTGCTG CTGCTGTTCA 960
GATCTGCATC CTGGTCCCGC TTGGTCCCAC AGTGAGAACG CTTTGCTATC ACATGGGCAG 1020
GCTCTGAGAG CCCTGCCGGC CTGGCCTTCT CAAAGAAGAC CTGAGAGCTT GGGACCCAAG 1080
CAGAGAGGAA GAACAGGGCT CAGGGTGCTT GCTCCATGCT CGCTCCACAC CTGGGGCTCA 1140
ACCCTGGCTT TCCCCGGCTC CCTGTGTGAC TTCAGGGCAG GTCCCTTGGG CCCTCTGGGC 1200
CTTATCATCT TCATCTGTAA CAGGGCGATG CCTCTGCCGT GTCTGGTGGT GTTGAGGAGT 1260
TCCTGTTTGT GTAAGCAGCT AGTTCAGTGC CAGCACGAGA TGGGAGGCCC ATGAAGTTAG 1320
CAGTGCACAA AAAATAGAGC AAAGACTGGA TGCATTTCCT GAGAACAACC ATCACTGTAA 1380
AGCACTTTAC AAATCCAAAG ACAACCCCCG GCAAAAACTC AAAATGAAAC TCCCTCTCGC 1440
AGAGCACAAT TCCAATTCGC TCTAAAAACA TTACAAGTTA GTTCATGTCA TGCCAGATAG 1500
CTGAAGGCAG CTCACAAGTT CTTAAGGCCA GGAATGCCAT GTGTCTGCTA TGCACAGCTG 1560
GCCCTGGCCC TGACAGCAAA GGTGACGCAG ATGTGGGTGC CCTGCTCCTG CCCAGCAGCA 1620
GTGCTTGGTG GAGGCTGAGG CCCTGCACAG GCACCCTCAC TGCTGACCTT GAGCCTCTCT 1680
|
