| Tag | Content |
|---|
EnhancerAtlas ID | HS184-10855 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr14:105435990-105437400 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr14:105436197-105436214 | CAGGGCAGTGTGACCCT | - | 6.03 | | ESR2 | MA0258.2 | chr14:105436198-105436213 | AGGGCAGTGTGACCC | - | 6.8 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_25065 | chr14:105436109-105437577 | Colon_Crypt_3 | | SE_26697 | chr14:105431767-105447222 | Esophagus | | SE_34348 | chr14:105432643-105444871 | HCT-116 | | SE_34827 | chr14:105432607-105444944 | HeLa | | SE_36459 | chr14:105432978-105441663 | HMEC | | SE_54999 | chr14:105431733-105444678 | Stomach_Smooth_Muscle | | SE_57490 | chr14:105436676-105437580 | VACO_503 | | SE_64788 | chr14:105433563-105441011 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGGAGCCAGT TGATGGGGAT GGGAGGGCAG CAGGTGGGCC CAGTTCATCT CCTTCTGCTC 60
CTGGAGAAAC TGAGGCACAG GGTAGCACAT GTGCCACCTC TCCAAGGGAT TTGGCAGCCA 120
AAAGGAACAG CCCCATGCTC CCATCCATCC CAGGCGGGCT AGCCTGAGCC AGTTTCCCTG 180
GGCTGAAAGG CCGGCCCCAC AGACGTCCAG GGCAGTGTGA CCCTGTGATG GAGCTACCCA 240
TCGCCCCAGG CCCCCACAGC CCACCTCGGG CACCCCCAGG AGAGTAAACC TGGCCTTTGG 300
AAGCAACCAC CCTCCACAGC CACCCAGGGC CCCTGTGCAC CAAGCAAGCA CACGGTCATC 360
TGAGGACCCT TCTCCAGGCC CCACGCCCAC CTTGGGGACT TGCAGACCTG CGGCTGCCCT 420
GAATGTGGGT GCTCTTGGCA TTCACCTCCC CCCACACCCA GGCTCCTTGG AAACAAGAGC 480
CACTGTCCCC TACCTGCCCA GGGCCCACAG CTTGGTGTCC TGCCACACAC CTTGTATGGC 540
CTGGGCTCCG CCGGCACCCC AGGGACCAGG ACCCAGGAGA AGGGGCTCCG GGGCTTTCTC 600
CCTGACATCC CTGCCCAGCC CGCTGGCCCT GGCTGGAGCC ACGGTGAACT AACACCCCTG 660
CCCGTCTGTC AGCTGCAGGT CGGGGGATGC CTAGCCCAGC TCTGTTCCTC CAGCCCCCCT 720
TGCTGGTGGC CTGCTGGCCC CCACAGACCC GCGGAAGAGT GAGGCAAGCA GGTGTCCGGA 780
CATGGACACA GGAGCCACTT ACCAAGGAAG CTACAGACGC TCTCCCAACT GGCCCAGAAG 840
CGAAGATCCC AACTGGCCAC CTCCCCCTGC CACGCCCGGT TCTTCCCTCC ACAGCTCCTC 900
CCCCCATTGT CCCGCCTCTG CCTGCTCCTA GGGCTGGCTC TGGACCCTGC CAGGACCCCC 960
ACATCCCACC AGAGGGAGTG GGCGGGTCCC CTGATGGGCC AGGAGCCTGG CCAGCCCCCA 1020
ACACTCACTC AGCTTCTTGG AGCTGGGGAC CCCACCCTGA GTGCCCACCC CCAGCCTGAG 1080
CAGCTGACTG CAGAGGAACA GACCGCTCTG AGTCACACAG CCAGCCCAGT CTGGTGAGTG 1140
CCTTAGTGTG CGCCAGGTCC TGCTGTGTGG ACAGACACAG GCCTGAGGCA GGTCCCTCCT 1200
AGGCAGGCTC TGCACAAACC CTGTGTCTCA GTTTCCCTAT GGGGGCCAGG ACAGAGGCTG 1260
GCCCAGAAGG GAGGAGAGGC ATAGCCTAAG GGCCTGCCCC CATGGTCACT GGGCCAGTGA 1320
CCTTGGGGCC TGGTCATCTG CCACCTGCCT GAGCCCCCAG GGCAGCCGAC CCTGGCCTCC 1380
CTTCAGCCCG CTCAGCCCAA ACTCACAGCG 1410
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