| Tag | Content |
|---|
EnhancerAtlas ID | HS044-11622 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr6:140029460-140030910 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr6:140030124-140030135 | TTTGACCTTGA | - | 6.14 | | ESRRB | MA0141.3 | chr6:140030831-140030842 | TTTGACCTTGA | - | 6.14 | | Esrra | MA0592.2 | chr6:140030125-140030136 | TTGACCTTGAA | - | 6.14 | | Esrra | MA0592.2 | chr6:140030832-140030843 | TTGACCTTGAA | - | 6.14 | | Klf1 | MA0493.1 | chr6:140030878-140030889 | GGCCACACCCA | + | 6.62 |
|
| | 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 |
| GH06I139707 | chr6 | 140028689 | 140031197 |
|
Enhancer Sequence | GACTGCCTTT TTTTTTGGAA TGGGATGGTG GTAGGTAGGA ACAAAAAAAA TGCAGGGATA 60
AACAAAACCT AAATTAATGT CTCAATTTGT TAACCCATTG CACTATCAGA GTACAGACTC 120
CTGGCAAGCA GATGCCAAAA TTGGTAACAT GTCCAGATTG GCTCCAGTCC AGCAGAAGTT 180
CAATTGTTGA AGAACATGTA TAAAGTCTTC TTAAATACTG TTTGGTCACA CCCATTCATT 240
AGTCTGGGCA TACTTCCTTT AGGGAGTACC AACCAGTGCC TTCTTTATTT TATATTAAGG 300
GTCACAGAGG ATGAAGTTTG GTGAGGCACT TCAGGGGGAT TTTCCAATGG GTTTGAATGA 360
GTCTTAGAGA AAATTGTATA CTCCAAACTC CTTGGAGAAG AGCTTCCTGG GATAAATGTT 420
AAATCTGTAT CAGAACAGAG CACAGCTCTT GTCACTGTTT GGTGCCTGGG TCTGCTGCTG 480
GAAAATTCCT CTTGCCTTAT GCTATCAAGT GAGCTAGCTA AATTCTGGAG AAAGCTGCTC 540
ATAAAACTGA TAAGAGCCCT CTGTTAAACA ACCTAATTTG AACTTTATCC CAGAGACCTT 600
GAGAAACAGG GTCTGCACTT TTATAATCCA AGAATTGAAT ATGGTCCTGC ACAGTTGGGT 660
AACATTTGAC CTTGAAACGT CGTTCTAAAA GTCGTGTTTC CCCCTTGCTG GCTTTGCTGT 720
TATCTGTGCA TCAGTGAACA CTTTATCATA GTAACGCTTC AGGAATGTGC AGAATAGTTG 780
AGGAGCTTGA ATGCCACAGC AGTTTCAAGT ATGCTGGGCT CTTGCTACCA GCTCACTGGG 840
TCGGTCGCTA GAAGACTGCT ATAGCACATA TGCTGCAGAA CTGACGTTCA TTACCAGGTC 900
ACTTTCAAAG TGTTGGCTAG CAAGTCTGTA GTTAGTTCTT ATTTTTCTCC TATGATTTCT 960
GTTTTCAACA AATTTGCAGT CCATTTGGAC AGGTAGAATA AACAGGGCAA ATAAAACCAT 1020
AGAAGAATTA TTGAGTTCTT CCTACTTCTT ATTATACGAA GGGCATGGTA TGCATTTTCC 1080
CCTTTAACAT AACATGCAAC ATCCAACAGT CTGGAAAGGT ATTATTCTAC CCATTTTGCA 1140
CATTAGGAAA CTGAGGCTTA CAGATGTGAA GATAATGACT CCAAGTCTAA CAGCTAGTAA 1200
ATTATAGACC TAGATTCAAA CCCAAGACTG TGATGACAAA CCCCAGGTGC TTATTAAGCA 1260
CTGCACTCTG TTAAACAACC TAATTTGAAC TTTATCCCAG AGACCTTGAG AAACTGGGTC 1320
TGCACTTTCA TAATCCAAGA ATTGAATATG GTCCTGCACA GTTGGGTAAC ATTTGACCTT 1380
GAAATGTCAT TCTAAATGTC ATGTCATAAA TACTGTTTGG CCACACCCAT TCATTACTCT 1440
GGACATCAGA 1450
|
