| Tag | Content |
|---|
EnhancerAtlas ID | HS044-09592 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr4:9604020-9606450 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX2 | MA0600.2 | chr4:9605756-9605772 | TGTTACCATGGAGACA | + | 6.03 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 9604160 | 9604200 | | chr4 | 9605472 | 9605800 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH04I009602 | chr4 | 9603949 | 9607947 |
| Enhancer Sequence | TCATTGAACC TCACAAGCTG TGTGGCAGGT TGTTACTAAA AATCCTAGCT ACCCTGATCA 60
GTTTCCCTAC ATTGATCAAT AGCTAAGTTT GGTCAGGAGC CCCCTCCATG GCTCCGCTCA 120
TGCGCCATTC ATAATTCTAC CTCCAAGTTC CGCCTGAGCC AGACCGCGTT TTTGCCTCGA 180
TCCTCAGCCG GTTCGGCTTC CCCCGTACTG CCTCCCTCTG AAGAAGAGGA GAGTCTCCCT 240
CACCCAGTCC CACTGCCTTA CAACCATCCT GCTCCCTTAA TGTTATCCCA TGTCTCCTCG 300
GGGACGTCCC CTGTAGGCTC GCCACCCATT GCCTCTCAAT CGCGACCGCG GCAGGAAGAA 360
GTAGCCCCTC TACTACCACT GAGAGAGTCA CAAGTCCCTC CAGGTGACGA GCGCTCAGCC 420
CCCTTCTTAG TTTATGACCC TTTTTCTTCT TCTGTCTTAT ATAATTAGAA AACCCATAAT 480
CCTCCCTTCT CTGAAAAGCC CCAGGCTTTG ACCTCTCTGA TAGAGTCCGT ACTCCGGACT 540
CACCCGCCCA CGTAAGATGA TTGTCAACAG CTCCTTTTAA CCCTTTTCAC CTCTGAAAAG 600
AAAGAACGTA TCCGAAAAGA AGCCAAAAAG TACTTCCTCA CATCAGCCAA TAGACTGGAA 660
GAAGAAGCTA GAGACCTCCT TGAGGAGGTC TTTCCGTCTA CCCGGCCCAA CTGGTACCCA 720
AATTCCTCAA GTAGAAAGAG AGCTTCAGAC GATTTTCACC GGTATCTCCT CGCGAGTATT 780
AAAAGAGCCG CTCAGAAACC CATAAACTTG TCTAAGATGA CCGAAGTTGT CCAAAGGCCC 840
GATAAGTCAC CAAGAACGTT TTTAGAGCGC CTCCAGGAGG CTTATCGGAT TTACACCCCT 900
TTTGATCCGG CAGCTCTAGA AAATAGCCGT GCTCTTAATT TAGCATTTGT GGCTCAGGCA 960
GCCCCGGATA TTAAAAAGAA ACTCCAAAAA CTAGAAAGAT TTGCTAGAAT AAATATCTGT 1020
CAGCTTTTAG AAATAGCCCA AAAAGCTTTT GACAATCACA AGGTTAAAAA AACAAAAACA 1080
AGCAACACAG GCAGCTGAAA AGGCCGCTGA TAAAGCATTC AAAAGACAAA CAAAAATCTT 1140
AGTGGCGGCT ATCCAAGAAG TACAGAATGA AATAGCCCGT TAATTTAGCA TTAACTGAAG 1200
CCCCTGCTTT AGCCCTCCCT AATATCTCCA TAAAAGCCAA GGAGTTGCTA AAGACGTGTT 1260
TACTCAGACT CTAAGACCCT AAAGACGCCC AGTGGCCTAT TTATCTAAGA GGCTAGATCC 1320
TGTGGCCTCT AGATGGCCAA GTTGTCTGCG AGCCATAGCG GCTACAGCAA GCCTAGTCCA 1380
AGAAGATGGT AAGTTAACTG TAAGCCAAAA TTTAACCCTT ACAGCTCTTC AAGCCATAAA 1440
GACCTTACTA CGAAGTGCTT CTGGCAAATA GATGTCAAAT GCTCGCATCT TACAGTATCA 1500
AAGTTTACTG TTAGATCAGC CTCGTTTGAC TTTCTCTCCC ACAAAGTGTT TCAATCCAGC 1560
TACACTACTT CCCGACTCAG ACTGCACTAT TCCTGCTCAT GACTGTCAAG AACTGTTAGA 1620
AACTATCGAA ACTGGCCAAT CTGATCTTCA AGCTGTGCCC CTAGAAAAGG CAGATGCCGC 1680
CGTGTTCACA GAAGTAGCAG CTTCCTCAAG CAGGAAGTAG GAAAAGCCAG TGCAGTTGTT 1740
ACCATGGAGA CAGATGTGTT GTAAGCTCAA GCTTTACCAG CGAACACCTC AGCACAAAAG 1800
GCTGAATTGA TCGCCCTCAC TCAGGCTCTC CGATAAAGAG TAAACGTATT AACATTTACA 1860
CTGACAGCAA GTACGCCTTT GCTACTGTGC ATGTACATAA AGCCATCTAC CAGGAAAGCA 1920
GGCTACTCAC CTCAGCAGCT AGCTGTGATC CACTGCAAAG GACATCAAAA AGAAAACACG 1980
GCCGTAGCCC ATAGTAACCA GAAAGCTGAT TCAGCAGCTC AGGTCGCAGC AAGACTTTCA 2040
GTCACGCCTC TAAACTTGCT GCCCACAGTC TCCTTTCCAC AGCCAGATCT GCCTGACAAT 2100
CCCGTATACT CAACAACAAC AAAAAAACTG GCTTCAGATC TCAGAGCCAA TACAAATCAG 2160
GAAAGTTAGT AGATTCTTCC TGACTCTAGA ATCTTCACAC CCTGAACTCT TAAAGAAACT 2220
TTAATCAGCC ACCTACAGTC TACCACCCAC TTAAAAAGAG CAAAGCTACC TCAGCTCCTC 2280
CGGAGCCATT TTAAGATCCC CCGTCTTCAA AGCCTAACAG ATTAAGCAGC TCTCAAGTGC 2340
ACAACCTGCG CCCACGTAAA AGCCAAACAA AGTCCTAAAC CCAGCCCAGG CCACTGTCTC 2400
TGAAAAAACT CGTCAAGAAA AAAGTAAGAA 2430
|
| |
|
|
|
