| Tag | Content |
|---|
EnhancerAtlas ID | HS092-27277 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr22:29490410-29491870 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBX21 | MA0690.1 | chr22:29490550-29490560 | TTCACACCTT | - | 6.02 | | TBX2 | MA0688.1 | chr22:29490549-29490560 | TTTCACACCTT | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 29491514 | 29491614 | | chr22 | 29490470 | 29490518 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH22I029095 | chr22 | 29491581 | 29491730 | | GH22I029091 | chr22 | 29487616 | 29491312 |
|
Enhancer Sequence | AAGATGGGGC CACTCAGTAC TTTAAAAAGA TAGATATATA TCTAGTCTCT TCTTCCAACC 60
CCTTTCATCC CAGCTCACAA CTAGGGGAAG TCTTTTGACC AACTCAAGAG ACTTATCTTG 120
TCAGTTTTAA AAATATTTCT TTCACACCTT ACACACACAC ACACACACAC ACACACACAC 180
ACACACACAC ACAATTTACC ACTCTTTTTT TTTTTTTTTG AGACGGCGTC TCGCTCTGTC 240
GCCCAGGCTG GAGTGCAGTG GCGCGATCTC GGCTCACTGC AAGCTCCGCC TCCCGGGTTC 300
ACGCCATTCT CCTGCCTCAG CCTCCCGAGT AGCTGGGACT ACAGGCGCCC GCCAACACGC 360
CCGGCTAATT TTTCGTGTTT TTAGTAGAGA CAGGGTTTCA ACCGTGTTAG CCAGGATGGT 420
CTCGATCTCC TGACCTTGTG ATCCGCCCGC CTCAGCCTCC CAAAGTGCTG GGGTTACAGG 480
CGTGAGCCAC CGCGCCCGGC CAATTTACCA CTCTTTTCAA CATGGGTTGT TTTAATGCTG 540
GCTTTGAAAG CTCTGCTTTT CTGTCTGATC ACTTCCTTGT CTCTTTGGGA GGGTTTTCTT 600
AGTTAGCCCT ACCACCAGTG GACAATACAC AGTTAGCAGA GCAGCCTACA CTACCGAGAA 660
TGTCGTGGTC AGACAGCACC ATGTGTGACC CAAATCTCCC TCTGCTTCTG AGCAAAGGAA 720
GCTGCCTACA TTGTTGTGCC TCCGGCCAGC CCAGGATAAC CTTGCTCTGG GAACAGCTGT 780
ATCCATCAGA TGTGTGCCAT TTACTTCCTT TTAGTCGACT AAGGTGTTTC TTTGCTTTTC 840
ACCTCCCGTC TGACTCTAGC AGGGGATCTT AACCTGACAT CTATGGTGCT TCAAAAGTGA 900
TTCACAATTT CCTGGGGATG ATCCATAGCT TTGATCAGCT TCTCAAAGTT ATCTGTGATT 960
GAAAACAAGT TCAGGATCAC TGGTATGTAG GGTCCAGAAC AAAGACTGTA AGCACTTTTG 1020
GTTATACATT TGTGCTGCTT ATGCCCAAGA TCCTGGTAAT GAGACTTATG GTTCAGCAAT 1080
GCATTGAATT TAATTATTAT TAGTACAGGT GCAAAGGCAG CCTCTTGAGC TACTGGGACA 1140
GGGAAAAATG ATTGTTGAAC TATATACCCT GTCCCTGGTT CTACATACAT TGGAATCTCA 1200
ACCATGGCAC TGTTGACGCA GCTGAGCCAA CATATATTTT CCTGTATTGT ATGGGCCACA 1260
CTGTTTACCT TCTGCCCTCT ACATACCTTT GCTAACGCTC TAGGGCCCTT GTAGTTGTCT 1320
CAAAGTCACC AGGCCTTTAG TCTATGTTTT CTTTATCCCT ATACCTTTCT CTATCTTGTA 1380
TCAACTGACC ATTCCCTCCT AGTTGCTATT GACTTATTTT GTTTGTTATA AAAGTGTTAA 1440
AAGCTTATTC TTAAAAAAAA 1460
|
