| Tag | Content |
|---|
EnhancerAtlas ID | HS183-06926 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr5:177634220-177635470 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr5:177635195-177635206 | GCAGGGTGTGG | - | 6.62 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23127 | chr5:177631436-177638056 | Colon_Crypt_1 | | SE_23791 | chr5:177633147-177637957 | Colon_Crypt_2 | | SE_24793 | chr5:177634329-177638520 | Colon_Crypt_3 | | SE_28105 | chr5:177630835-177643084 | Fetal_Intestine | | SE_28930 | chr5:177630824-177643883 | Fetal_Intestine_Large | | SE_50201 | chr5:177630779-177644241 | Sigmoid_Colon | | SE_52441 | chr5:177630834-177644193 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGCAAGGTAA GGTGTTCCCA GCTCTGCTTG GCCTCCTGTG CTGCTGGAGA GCTGGCCCTT 60
AGAGGGATGG GTTAGGGGTT GGGCCTCATG CAGGAGCTCT CCAGGTTGGT CAGACTTTAC 120
TATTTCTCTG AAGCGTATGC TGCCCTGATT GGGGCAGTGT TCCAATCCTT GAAAGACTTC 180
TCAGGCTGGG AGGACTGCCA ATAAACAACA CAGGATGTGA GGGAGGTAGG AGAAGGTGGC 240
CTCTGTGAAT AGAGCAGGTT GAGTAGCCTC TTTAGCTCCT CACTTAAAGC TAGAGGTGAC 300
AGTTCTAGAT TCTTGAGTCC AGGGGTATGA AGCCTGCAGT TTAAGGTCTC AGAAGATCCT 360
AGAACTTCTG CAACTCACTG ATTCTCCTCT GTGGTGAAGT TTTTCTTATT CCAGAGCCTT 420
TCTACCTCCT TCTACAACCA AGTCTTTGTC CACTTCCATC CACTTTGAGC ACTTTTTTTT 480
TTTTTTTTTT TTTTTTGCTT TGAGACAGAG TCTTGCTTTG TTGTCCAGGC TGGGGTGCGG 540
TAACACAATC ATGGCTCACT GCAACCTTGA CCTCATGGGC GGACCGGATC CTCCCATCTC 600
AGCCTCTCGA GTAGCTGGGA CCACAGGCAT GTACCACCAT GCCTGGCTCA TATGTTTTTT 660
TAAAGCCTGG TCTCACCATG TTGCCTGGGC TCAAGCCATC CTCTGCCTTG GCCTTGTAAA 720
GTGTTGGGAT TACAGGCATG AACTGCCTCA CTTGGTCTTC TGGGCACCTC TTTAAGTTAA 780
CCCTAAACCC AGGCAAAAAT CCTTCCAAAG ATCTCCCAGG GTCCTGGCCA GCTTAAATCC 840
AGGGTCAGTT GTGCTTTCAA ATGAGTGGAT TCATGTGCAG GGAGGTGTAG CTCTTCCCCT 900
CCTGAACTCT GGTCAGGGAA AGGGTAGTTC AGGCTTCAAG TTGGCAGTTG GGAGTTGAGG 960
GTGCGGCCTG CAGTGGCAGG GTGTGGCAGG TTCTGTTTCT GAGCAGGAGT TGGCAGCCAG 1020
ATAAGGTGGG ACAGGTGGAA CTCCTGGAAG TCTCTATCCT GGCTGGGAGT TTGGAAAGAG 1080
TGGATTAGGA TAGTCTTAAA TTTTCTATAA AATGACAGTC TTTGAGGCAG TTAGGGGAAG 1140
CAGTGGTTAT TACTCCAGTG GACAGTGATA GAGGCCTTTT TCTCTATGTG CCATAATGGG 1200
AAATGGGTGG GAAGAGCCTC TAAGGCAGAG TTTAAGTGAA ACTACTGGTA 1250
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