| Tag | Content |
|---|
EnhancerAtlas ID | HS183-06934 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr5:177649930-177651440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SCRT2 | MA0744.1 | chr5:177650564-177650577 | ACACCTGTTGCAA | - | 6.06 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23127 | chr5:177649156-177656171 | Colon_Crypt_1 | | SE_23791 | chr5:177650723-177651894 | Colon_Crypt_2 | | SE_24793 | chr5:177650599-177652021 | Colon_Crypt_3 | | SE_28105 | chr5:177647910-177650934 | Fetal_Intestine | | SE_28105 | chr5:177650978-177655881 | Fetal_Intestine | | SE_28930 | chr5:177647618-177656175 | Fetal_Intestine_Large |
|
| | 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 |
| GH05I178220 | chr5 | 177647239 | 177655858 |
|
Enhancer Sequence | GCAATCTGTG AAGAGATGGA CATTGGGAAC ACGACCATGG GGTTGTGCAG TGACCGGCTT 60
AGCGTGCCCT GCTAGTGCTG GCTTAGTCCA AGCAAGACAA GTCACCATCA GTGCTGCACC 120
CCTACTTTGG GTTCCATGTT ACATCTGAAG GTTTGTGACT CAGTTTTCTC TCAGGCCTCC 180
AGCCAACTCT TACTACCTGG ATGCCTCCAG GCCCCTAGTA CTTGGCATGC CCCAAACTAC 240
ATGCACTGAT TTTTCCACCA TAAGCCAGTT CCTTCCCTGT CCCCCATTTT TGATCCACGC 300
CTCCTCCCTC AACCCATCAG TCAGCACTGC CCAAGGATTC TACCTCAGCC CCCTCTCTAA 360
ACCTACTCCT TGCCCTCTGC CTGGACATGC CTGCCTCCTG CAGATTTGCC TGTTTCTTCC 420
TTGGACTCCT GCAGAGGTCT TCTAACTGAA TGCCTTTTCC AGTCCATCCT CCACATGGCC 480
ACCAGGGTGA TGATGCCTCA ACCCAGAGAA CTGAGCATGT CACTGTTGTT TAAAACCCCT 540
CAGTGACCCC TTCTGCATAT GGCAATGATT TCCCAACCAT ATTCTGCCTT ACAGGTGGGA 600
GGGCAGGGCC AATGGGATGG GATACTGGTC CCCCACACCT GTTGCAATCA GAGCAATCTC 660
CTTTTTTAGG TTTTATAGAA GTGGTCGCAG AGCACCTGAA ACACACAGGC AAGGCTCCCC 720
TGGTCGGGTT CTGCTAACCT TTCTGGCCCC ACAGGCTGCC TTTCTTTGTC GTACCTCCTG 780
TGTCTGGCTC TGTCACTCCT TCAGTGAAGC CTTCAGAGAG CCCTCACCTG TCGCCAACAG 840
TCTTCCCTCT GTTGTCACCG TAGGTAACAC ACCTCTCTCT CCTATGTCTG CGCCTCCACT 900
CCATCTCCAC CATACTGCCC CCGTCAGGCC TCCCCACAGC TCACTTGGGG CCTGCTGGCC 960
ACTTCACGGT CACCTGACCT CAAGCCGCCG CATTCCAATC CATCCTCCAC ATAGCCCTGG 1020
AGTCAGAGAG CAGCCCCGGC CCCAGGTCTT AGCGCTCTCC TGCTTAAGAC TCTGGTGGTT 1080
CCCGGGGGCC TCCAGGGCAG AACTGCTGCC GCCCAGCATA GTTCCGGTGC CCTCTGGCAT 1140
GTGGACCCTG CCTGCCTCTC CAGGATCAGC TCCTGGCCAC ACATTCACAC GGTTCCTCAG 1200
CCACCCAGTG GGATGCCCTT CCTCTGCTAC TCCCCACCCC ACCTGGAGTG GCTGACCCCT 1260
ACTGTGTCAG AGAGCACCCC CTCCAAGGAC CCCGCTTGGT ACCTCCCAAG GCCTGCTCAG 1320
GCTCTGGCTG GCTACCACGC CCATGCTAGG CCGTGCACTC AGACTCTCTG CTGAGCCCAA 1380
ACTGCCCCTA TCCCAGATTC CTGGAGGGCA GGGCCTCGTT TGGTTTTCTC TCTGGGTTCC 1440
CAGCATCTAG CACAGTGGCG GTGACAACGG AGGTGACATT CACTGTTGGC TGGATTGGAC 1500
AGGCGCGGAC 1510
|
