| Tag | Content |
|---|
EnhancerAtlas ID | HS042-41023 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr6:137026920-137028140 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr6:137027685-137027701 | TGTTGCCATGGAAACA | + | 6.89 | | RFX1 | MA0509.2 | chr6:137027685-137027701 | TGTTGCCATGGAAACA | - | 6.91 | | RFX2 | MA0600.2 | chr6:137027685-137027701 | TGTTGCCATGGAAACA | - | 7.11 | | RFX2 | MA0600.2 | chr6:137027685-137027701 | TGTTGCCATGGAAACA | + | 7.17 | | RFX5 | MA0510.2 | chr6:137027685-137027701 | TGTTGCCATGGAAACA | - | 7.05 | | RFX5 | MA0510.2 | chr6:137027685-137027701 | TGTTGCCATGGAAACA | + | 7.06 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TAAAACGAGT TTGCTTTCCC TAAGCACAAT GTCTCTCACA CTCTGGGAGG GGAAAAAACA 60
GTGTGTTACA TCCTGAGCAG CTAGAAATAA AGGGTATTGG CCACCGGCAA ATCCACACAC 120
AGATAATCAA GACATCTGAC AAAAAATAGT CATAATTTGT GTGTTTTTCA TTGAGAAATA 180
TAATGGGATA AATGGCCGGG TGCAGTGGCT CATGCCTGTA ATCCCAGCAC TTTGGGAGGT 240
GGAGGCAGGT GGATCACCTG AGGTCATGAG CTCGAGACCA GCCTGGCCAA CATGGTGAAA 300
CTCCATCTCT ACTAACAATA CAAAAATTAG CTAGGCATGG TGGCACATGA CTGCATGACT 360
GTAATCCCAG CTACTCAGGA GGCTGAGGCA GGAGAATCAC TTGAATCCAA GAGGCGGAGG 420
CTGCGGCGAG CTGAGATCGC ACCACTGCAC TCTAACCTGG GTGACAGAGT GAGACTCCTC 480
AAAAAAAAAA GAATGGGATA AGTACACAGT GTGGGCAGTG TGCCCATCTT CTAGGTTGTG 540
AAGATTGAGT GAGATCATAC AAATAATATA GCTATACAGT GCCTGACACA TAAAAGCTCT 600
CAATATAAGC TAACTATCAG TATTGTTATT CCTATACCTC ACCATGACTA CAGACACCGG 660
AGAGACGATC TAGAAAAGCC TGTTGTATCA AGGCTTCACT GAGGTTGGGG AATCATCATT 720
TAGAAAAGGG AAAAGGGAAC AGCATATTGG AAAGGATGGC ATGAATGTTG CCATGGAAAC 780
AGAAATAGTA AGGCATTTGT GGAGCCTCAA GGGCGAGTCC ATCTGGCTGA GGCAAGGAGC 840
CAGATCTGGG AGGGAAGAGT GTGGCCAGGC GAGGCCCGGC TGAGTGGCCA TCATCTTCAG 900
CCCAGGACCA GGATGCTGAA TCCACATGGG GCAAAGAAGA ACCAACAAGG ACTTTCATGC 960
AAAGGAGCAT GTAAGATTTT TGAATGTTTA AGGATAGCAG ATGAGAAAAC AAAAACTGAC 1020
AGAGGAAAGA ATTGCACTGG GTAGTTCTGA GGGCCATGAA GATGTACACA AAACACTAAA 1080
AATGCCTGGT GCCGTGGCTG ACGCCTGTAA ATCTCAGCGC TTTGGGAGGC TAAGGCCGGA 1140
AGATCACTTG AGACTAGGAG TTTGAGGCCA GCCTAGGCAA CATGATGAGA CTCTGCCTCT 1200
AGAAAACATT TAAAAATTAG 1220
|
| |
|
|
|
