| Tag | Content |
|---|
EnhancerAtlas ID | HS044-07188 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr2:72498720-72500220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA(var.2) | MA0730.1 | chr2:72499031-72499048 | AGGTCACATAGAGGTAA | + | 6.12 | | ZNF263 | MA0528.1 | chr2:72499082-72499103 | CCTCCCCTTTTCCCCTCCCTC | - | 6.56 | | ZNF263 | MA0528.1 | chr2:72499086-72499107 | CCCTTTTCCCCTCCCTCCACT | - | 6.61 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 72498860 | 72499637 | | chr2 | 72499643 | 72499967 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I072270 | chr2 | 72497941 | 72500118 |
|
Enhancer Sequence | ACTGTGTCCT TTTGATTTTA GGGAAAAAAA AAACCCTTGT TATGTTGGTC CTTATATAAT 60
GTAAAGTAGC CTGTTTACCT CTAGAGAAAA ACTCACGTTT TCATCTTGAC AAATACTTCT 120
GGGTTTGCAC ATATACCACA ACACATTATA CATATTTCAA GATCAAAACT GCACCTGCAG 180
TTCACAATGA CCTATATTTT GCCTTGGTCC CCGAAAGCTG CTCTGTAGCA AAGCCAAGTC 240
AAAACAATGC TCAAGGAAAA AAAAAATGCT GAAAGTTCCT GGCAATTTCC CTTCCACTCC 300
ACATGCTGCC AAGGTCACAT AGAGGTAAAG CTGAACTCTC CATTTGGCCG TTTTTGCTTT 360
TTCCTCCCCT TTTCCCCTCC CTCCACTTAC GTACATGCTG ATATAGTTTA TGGTCTGTAC 420
CTCAATAGCA TTATCACTCT GGGTTTTTAT CAGACTTGAG GTCAGTGGAA GTAGGAAAGG 480
AGAATGGATG TGAGTCTGGG TGTGGCAAGT TCCTATTGCT TTATCAGGGA GGTAAAAAAG 540
TGAATCCACC TAGTATGCTT CTGGCTGTGA AGTGCAGTGA GGTGAGCCAA GGTGCCAGGG 600
GGTCACTAGG AGTTCATCTT GGATAAGTGC CCAATGTTTG CAGGACTTAG CTCATCAACT 660
TTTCTAATTT GCAAAGATGT ATTTCCTGTT GGGTTTCTTC ATCCCTGTCA TCTAGGGAAA 720
ATAATCCAGT ATGCAGCCTG TTTGGTGTGT ACAGAAAACA TCCCCTTCCT GAATTAAATC 780
CAATTATGGT AATTCATTCA GCAAATCCTG TGATCACTGG CACAAGTTAA ACTGCACAGG 840
GTGGAGGAGT TGGGTGTTAA GCAAAGGGGA CTATCTGTCA AGTATACCTA GGTGCTTTCC 900
TCATCACTGC ATTGACCTGT ACCTGAACCT ATTCAACATC ATCTACAAAC TACTTAACCT 960
TGGTGTGCCG TGTTTTCGTC TCCTATAAAA CAGCATTTCT CACTGTTTAT TCCTAAATTG 1020
CTTCTGTTAC CTGCTTAGAG AGCCCTGGAG AGTAGAACAA CTAAGCCTTA GTAACAGGAA 1080
AAGAACACAA GATTAAATTT TAAGAGTTGT GCTTCTGGAT TTTGAGACTG AGAGTTGGCT 1140
GACGGGGGAG CCCTATGGGC TAGCCGTGAA TAGGATGTTA TTGGCATCAT TCTTTTGTGC 1200
TAATTTATGG TAGAACTGGC CATTGCTTGG GTCTTACTAT TAGATTAGAA TGATTAAAAG 1260
TACAAAGCAG GTGGGAGGAA TACTGAATAA TTCCCTCCTA TTAAGTTTAG GTCAAAAATA 1320
TTGCAGAACA CTAAGGAAAA GTGTTCATTT TCTGAGACAC TGCATTAAGG AGAAAGTAAA 1380
AGGTGAGATT TTAGACTCTG CTCTCCCAGT TACAGTCACA CTGCCCTTAC ATCTTTTCAC 1440
CTGACCTACT TTGAAATCTA GGTGTGATAA ACTATAATGG CAATAATCAC TTCCACTCAA 1500
|
