| Tag | Content |
|---|
EnhancerAtlas ID | HS092-38919 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr9:131667300-131668600 |
Target genes | | Number: 32 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr9:131668355-131668370 | TGACCTTTGGTCTTC | - | 6.12 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr9 | 131667633 | 131667800 | | chr9 | 131668475 | 131668589 | | chr9 | 131668289 | 131668550 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I128905 | chr9 | 131667537 | 131668604 |
|
Enhancer Sequence | AATTAGCCAG GCATGGTGGC ACACACCTGT AGCCCCAGCT ACCTGGGGGA GGCTAAGGTA 60
GGAGGATTGC TTGACCAGGA GGTTGAGGCT GCAGTGAGCC ATGATCACGC CACCGCACTC 120
TAGTTTGGGC AACAGAGCAA GATCCAATCT CTTACAAGAA AAATTATAAA ATTATAAAAT 180
ACACAGAAAG GACTGGAAGG TTATTATTCA GTGAAAAGTT AACAGTGTGT AACCCTGGTG 240
GGGATTGTAA AGCGGATTCT TCTTTTTTTG CTGCTACGCT TTTTTACAAT TTTCCGTATG 300
TTCTCCAGGG AACATCTAGT ACCTTATCCC TCCGTGACAG CCATACGTCT TTCATTGTAA 360
GAGCAACCAG CCTTGGCCGT GTGACCACGA ATGGCCACAG AGAGGCATTC TCACAGAGAT 420
CTTGCTGCGT GCCTCCTGTG TAGCACAGTC TGGGTTTCCT AATGTGGCTT CTCAGCCAGT 480
GTTTCCCAAG CTTGGCCAAT CATTAGAGTC ACCAAAGTTA TGTGTTAAAA ATCAGGTTCC 540
CAGCCAGGCA CGGTGGCTCA CTCCTGTAAT CCCAGCACTT TGGGAGGCTG AGACGGGCAG 600
ATCAGGAGGT AAAGGGATCG AGACCATCCT GGTCAACATC GTGAAACCTT GTCTCTACTA 660
AAAAACACAA AAATTACCTG GGCATGGTGG TGCAGGCCTG TAGTCCCAGC TACTCGGGAG 720
GCTGAGGCAG GAGAATCACT TGAACCCTGG AGGCAGAGGT TGCAGTGAGC CGAAATGATG 780
CCACTGCACT CCAGCCTGGC GACAGAGCAA GACTCCGTCT CAAAAAAAAA AGAAAAATCA 840
GATTTCCAGC TTCTCGCCAT AGTAGTCAAA CTAGACTCTC TCTGGGAGAG CCTGCTGTTG 900
CTGCTGTTTT TAATTCCTTT ATACACACGC AACCAGAGAT GATTTTACAT TAAGGCCTCT 960
CTGTGATCAC CCAGTTTGTG AGGGAGGAGA GCCTTATTCT TAATCCCCTC TCTTGAGGCC 1020
GCTCCCCTAG GAGCCTGTCA TTAAGACCCA CTATGTGACC TTTGGTCTTC CGAGTGTTCC 1080
CAGAATCTTG TACACACATA ACTATACACA CATGTGGAAT TTTGTTGTTG AAGCAGGGTC 1140
TCTGTCACCC AGGCTGGAGT ACAGCGACGG GGTCATAGCT CACTGCAGCT TCAACCTCCT 1200
GGACTCAAGC GATCCTCCCA CTTCATCCTC CCAAAATGCT GGGATTACAG GCTAGGATTA 1260
CAGGCGTGAG CCACCATGCC AGCCCCCATG TGGAATTTTT 1300
|
