| Tag | Content |
|---|
EnhancerAtlas ID | HS044-02630 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr11:85483280-85484680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr11:85484148-85484169 | TGAGTGTTTCACTTTCCTTTC | + | 6.15 | | TBX2 | MA0688.1 | chr11:85484397-85484408 | TTTCACACCTC | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I085771 | chr11 | 85482446 | 85484801 |
|
Enhancer Sequence | TAAATTTGGT TAAGAAGAAA GGTTCATAGT ACAGTCTAGA AGAAATGAAG AATGCTTTTA 60
CTTCGCCTAT CTTCATATAT ATAGTTCCTG AGACACAATA GGAAGTAGTA TTCTACTTGT 120
AGAAAACAAA TAGCCACAAG CATGCTCCCA TTGAATAAGT CTTAATGAAT ATCTGACTTG 180
CTATCTATGA AGTCCTATAA GGTTGTATTA CTAAATAAAA GGTGCTATTA CATGGTAGTT 240
ACACCAGTCA GTCAGCACCA ACTCTGCCCA GGCATTATGT CTCTGAATCT GCAAAATCCA 300
GTCATCCTTC ATGATAGCTG TCATATTCCA GAAGGACCTT CACTATGCGT ATGAAGGCAG 360
AATGACCAAC CATATCTAAA ACTCCATTTA ACATTAGATA TCAAAATGGG CAGCAACCAG 420
CCCAGCCCCA GTTTTGTTTT CCCCAAACTC CAGTCCCCTT ACTTATATCT CAGGCCAGCC 480
TGAGCTCAGA CTCAGTATAA TGCCTCACAG AAGGATAAAA ACCCTAATGA GCAAATTTCA 540
TAAAATATTC AGCTGGCCTT TTGGAGAAAA ACAGCTGGAG CTAACCTTAG GAATTCCACT 600
AATTCCCCCT ACCACACAGC CTAAAAATAG CCAAAGAGCA TTTCTTGCTA GTGATGGCCT 660
TTCCTTTAAA GGAAATAATA TGCAAAAGGC ATGCTGGGGT CATTAGCCCA AACCATGCAG 720
TCCCCATGAT AAATCCTTGG CCAAATGTTC CTATGAGAAT CTGCCTTCAT AAGGTCAACA 780
CTGAAATTTC CTTGGGAAGG TTCCCTTCTC CCTACTTCCC ACTGTATAAA AGACATAGGT 840
TATCAGCCAC TAATTCCCTG TATGGCCATG AGTGTTTCAC TTTCCTTTCC TTTCCTTGGC 900
CTCAGTTTCC ACATCTGCAA AAACAAGAGG GCTCAGTTCT GACCTCTAAG GTCTTCTGCC 960
ATTGTAAGAC TCCCTGGCAG GTACAGTCAA TGGCTTCACT GCCTTCAGGA TAAAATTCAA 1020
ACCACTCAGC GTTACATTAG CCCCTCCAGA TCTACACCCT GACTTCCTTT CCATTTCTCC 1080
CGACACAGTA CCTTGAAGTT AGTTCTTTAA ACTTACCTTT CACACCTCTG TCTTTGGAAC 1140
ATGCAGCTCC TTTTGCCTGC AAGGTCTTTC TCCAGCTTCT TAAACTCCTA GTCATCTTTC 1200
AAGACAGAGT CCAGGTGTCA CCTCCTGTCG GAAGATGAGT CTAGCCCCTT CCTGATAAGT 1260
GGAGTTAGAG TCTCCTCCTC TTTGGTCTCA CAGGACTCGG CATTATATAG CAACTGTCTG 1320
TTTCCTTATC CGTCTCCTTT ATCAGCCTGA GCTCTCCTGG AAGAAGGAGA TGCCATGTTC 1380
ATCTCCTCTG TATTTCCAAC 1400
|
