| Tag | Content |
|---|
EnhancerAtlas ID | HS044-10351 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr5:55811560-55813390 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr5:55812343-55812354 | TTAATCCTCTT | - | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_29188 | chr5:55811337-55814019 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I056515 | chr5 | 55811787 | 55813608 |
|
Enhancer Sequence | TTTTTCTCTT CCCACCTAAC CTCCAGATTC CTGACTTGTT TCATCCTACT GGTTCTTTTC 60
AAATTATACC TGTGATAATT CAGCTGTTAA AAGAGGAGTT TTGAAGTCCT GTTAATACGT 120
GACTCGAGGA AAATCCAAGG TAGGGAGAAA AATTAAACTC CTCCACCGCT CTGGGGAACT 180
TGGCTTTCTA AGGAGACATT GTTTTGAAAC CAAGAACAAG CCAGAGATGA CCAAGATTAG 240
GTTTTATACT TTGCTTCTCA AGTCCTGATC CTAATCCATT AGAGCTAATT TTGCCTGATT 300
CCTTTTCTGT ATGCTCTGGG CTTGGGTGGG TTTCTCTTAG ATGGAGGAAG AGTCAGGAAA 360
TGGGTTATGG GGAGGGAGAA AGGGACAGAT TTCATTAAAC TGCCAAAAAT AGGTTTATGC 420
CAGTAATAGC ACGTATGATG CAAACTTGCT TCTACATGCA GAATAATCAT CTGTATGGGA 480
AGTTGCTTAT GAAGATGATG ACATTTAAGA GTTTGGCATC CCAGCAGTTT TACCTTTGAT 540
CTTGGAAAAC TGCCCAAAGT AACTAAGTCA TTTACAATCT GCCTTGCTTG CCATTTGAAT 600
TATTTTGAGG GTTGAGGGGG CACTTTCTTC TTCATTGTGC ATTACCGGAG GCCTACTTTC 660
TGATCTAAAA GAAGCAAAAT AGGTGAGTCT CACACTCTGT GATTAAATAA CACAAGCTTT 720
GCTCTACAGT GACCTTATTT ATACTCCAAA TGACAGCCTA CAGCAGATCG CATTTGACAA 780
ATTTTAATCC TCTTAAACTG AAGTCTGAAA CAGATACTCG ATAGGCTCTT CATTGCGCCA 840
GAAGTGACAA TGCTGTGCTC CTCATGAGGC TCCAGTGGAA GCTGAATCCT CACAGAGGGG 900
CAGCCATCTG GGACTCTGGG TGGAGGCCAG CCCACAGCTC TACACCTCCT GTCTCACCTC 960
CACTCAGCTC TGAGGGTGGG CTGAGGGCAG AAGGAAGTGG AGCTGGAGTT GTAGAGACAG 1020
CGGTTTAGTG GAGGGCTCTC TGTCCTGGCT AGTTGAGGTG CGTGATGGGT AGTGGCAGAG 1080
AGAGGGGGTA GGGAGTGGGG TGAGGGAAGT CCAGGGAGCC CCGACAGGTG GAGATGGGGA 1140
AGTTGGGAAG ATTGGAAAGA GAGCGTGTAA AGGCAATGAA ACATTTCCCC TGCTCCTGAA 1200
GAAAAACATG GACGAGGAAG ACATGGATGT TGAGGCTTTA AAGCTGACTT TAAGTAAGGG 1260
AGATTGTTCC AGATTATCTG GGGGCCTGGT TCACTCCACT GAATGGCCTT CAGAGCAGAA 1320
CTGAGGCTTC CTGATGAAGA AATTCTGACT GTGCAGAGCA ACTTTGGCCC GTGTCCAAGA 1380
GTTGAAGTCT GTCTTTTCTG ACAGCCTGCC CTATTGATTT CAGACTTGCC TATCCAGTCC 1440
CCATAATCAG GTAAACCAAT TCTGTGCAAT AAATCTGTTA ATATCTGTCT CCTTCTGATG 1500
TGGTTTTACT GGTTAAAACT TGACTGATGC AGATTTGCAG CCTGGAGTCC CCTTCCAAAC 1560
GTGAGAATTT GTGGCTTCAG CTGCTGGAAG CCTGGCTGTG GCAGAGGCCC TCAGCTGCCA 1620
GCTGTCCTTA GGGAGTGCTT TGACTGAGCA GAGTCCCCTT GCCCCAGGTC ACACTCCCTT 1680
CCCAGGGCAG CAAAGCTCCA ATGACTGTCT GATGTGGGGC TAGAAAGGCT GGGCCCCTGG 1740
CCCCAACTCT GGGTAAACCC AAGGGCTGCC TCAGCTTCAG AGCTCCCCAT GAACTTGGCT 1800
GAGACCTTCA TTGTGGCTGC ATCATAGCCC 1830
|
