| Tag | Content |
|---|
EnhancerAtlas ID | HS047-29358 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr6:89754170-89755620 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr6:89754644-89754656 | TGCTGTGATTTA | - | 6.27 | | Gfi1b | MA0483.1 | chr6:89754644-89754655 | TGCTGTGATTT | - | 6.62 | | Nr2f6(var.2) | MA0728.1 | chr6:89755047-89755062 | GAGGTCAGGAGTTCA | + | 6.22 | | Sox6 | MA0515.1 | chr6:89754748-89754758 | CCATTGTTTT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 89754563 | 89754924 | | chr6 | 89755402 | 89755578 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I089044 | chr6 | 89753987 | 89755578 |
|
Enhancer Sequence | GGGATTCCAG GCATGAGCCA CCACGCCCGG CTTCATTTTT CTTTTTGATC CTGAATATTT 60
CACGTTCTTT TTTTTTTTTT TTTTTTTTTT TTGAGATAGG ATTTCACTAG TTGCTCAGGC 120
TGGTCTTGAA TTTCTGGCCT CAGGTAATTC TCCTGCCTCA GCCTCCTGAA CAAAAAAAAA 180
CACAAACAAG CCAGGGTTTC CTTCAAAGAC ATATTCACCA ATGTAGCTAT GTCTGCCTTC 240
CACCTGGTAT TAATCTGCAC ACCTTGTGTA CTTGTTTCTG TATTCCTGCA GGTGTTCGCT 300
TGGTGACTGT AACACTATTT TCCTGTAAAA GTCCTTGAGG GCTGTCTTAT TCCTCAGTCC 360
TCAGGCCTTC TCCGCCCACC CTGCTTCTTC TGAGAGGGAG TGGTCCGCCA GCCTGAAGCT 420
GACCTATTTT TCAAAACCAC CCTTTTCCTT AGGGTGGTTT TTCCTTAGAG GCTATGCTGT 480
GATTTATTTT TAAAGAACAG CCTTCTCTTG CACAGACCTG GGAGGTAAGC TACTCCAAAT 540
TACGAAGAAG GCTTCCACCA ACAAGACAGA TCTAAGAACC ATTGTTTTAG GTCTGCATGC 600
TTTTGAGCAC AAAGAGTAAA CCTTCCTGCA GCTTCGGAAT ATCTCTCTTC CTCTTTCAAA 660
GCCCTTTCAC AGCTTGGACT TGCTTCCTTT TTAGAGCCAC CCTCTCAGAT AAGGGTGGTT 720
TTAGAAGTAG GAAGCCAGAT TTGGGCGCAG GACAGAATGC TCTGAGCTCA GCCTGGCACG 780
GTTGCACAGT GTGGTGGGAA GCAGACTGGC CTGGCTGGGC GCAGTGGCTC AGCCTGTAAT 840
CCCAGTACTT TGGGAGACCC AGGAGGGCAG ATCACTTGAG GTCAGGAGTT CAAGACCAGC 900
CTGGCCAACA TGGTGAAACA CTGTTTCTAC TAAAAATTCA AAAATTAGCC AGGTGTGATG 960
GCTCATGCCT GTAATCCCAG CTACTCGGGA GGCTGAGGCA GGAGAATCAC TTGACCCAGG 1020
AGGCAGAGGT TGCAGTGAGC TAAGATCACA CCATTGCACT CCAGCCTGAG TGACAGAGCA 1080
AGACTCTATC TCAAAAAAAA AAAAAAAAGG TGGGGGAAGT GTATTGGCCT CTAATCCCAG 1140
CTCCAGCAAT TACGGCTTCT TCCTAGGCTT TTGTGTCCCT GTGTGAGAAA CATGGACCAG 1200
AAGTGCCATC AAGTTCTCGC TGTCCCTGTT CTTCAAATGA GGACGTGAAG CCATGGAGAT 1260
GGAAAAGTAT GATGGTGGGT TCCTCTGAGG CTGTGTCAGA GGAGACAAGA GTGGATACTG 1320
AGGATGATTC ATTAATCTTT CTTGGCAAAG AAAATTTTAT GTGATGACTA GAAATTTGTT 1380
TACTCATACA CAAATTCCTA CCGAAACAGT CGAGAGGAGA GAAATAGCAC ATTGGTACAA 1440
ATGTTTTTTC 1450
|
