| Tag | Content |
|---|
EnhancerAtlas ID | HS116-06630 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr11:67913490-67915000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELF5 | MA0136.2 | chr11:67913694-67913705 | ACCAGGAAGTA | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr11:67913579-67913594 | TGAACTCCTGACCTC | - | 6.22 | | RARA(var.2) | MA0730.1 | chr11:67914025-67914042 | TGACTTCAGGGTGACCT | - | 6.02 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_06593 | chr11:67913517-67915261 | Brain_Hippocampus_Middle | | SE_23262 | chr11:67913531-67915399 | Colon_Crypt_1 | | SE_27927 | chr11:67912746-67915438 | Fetal_Intestine | | SE_31508 | chr11:67912040-67918103 | Gastric | | SE_35342 | chr11:67911985-67915436 | HepG2 | | SE_42889 | chr11:67912022-67915452 | Lung | | SE_47694 | chr11:67913554-67915179 | Pancreas |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I068144 | chr11 | 67912141 | 67916582 |
|
Enhancer Sequence | CTGGGATTAC AGGTGCCCAC CACCACACTC AGCAAATTTT TTGTATTTTT AGTAGAGACG 60
GGGTTTTGCC ATGTTGGGCA GGCTGGTCTT GAACTCCTGA CCTCAGGTGA TCCGCCCGCC 120
TTGGGAGGCT GGGTTTTTGA GCTTTGTGCT GTTGGGGCCC AGCCCTCAGG GCCGCGTGGG 180
AACCCCCGGG GCGGGGTGTT CTATACCAGG AAGTAGGCAG AGGGCCAGCC CGAGGACAGT 240
TCGTTTCTTG CCAGTCCCCT GACCTCTCTT GGCACACAGC CTGTGGCAGC AGCAGGTTGA 300
AGCCAGACGC TGCTCAGACC TCACACCACG TCGTTTGCCC AACCCAGAGA AAGCTCTGTC 360
CCCGGCTTCT GGCTCCTTCT CTGCCAGGAC TCACTGGGTG TGATGAGTTG GTCTTGGGGC 420
ACTGTCTGGG CACAGCCTGT TTGCCCAACA TGGCCTCCTG GGCTCCATGC TTCCGCAGGT 480
GGGAGGGGTC TGGACTGGCC CAGGGGCTCT GACAGCGGCT GGCAACCTGA GGTTTTGACT 540
TCAGGGTGAC CTGAATCCTG CCGCATTATG GAGGCTGGAG TCTCTGGGGG CTGCTTTCCC 600
AGAGAAGAAG CTCCTTCCCC ATCAGCCTGA CATTGGCTCC AAGGACTCCA TGTGGCTGGA 660
GGGCTCAGGG CTAAGGGGAG GGAAGCCCCG GGATGGCAGT GAGGGGTGAG GGAAGATTTG 720
GGAGGTGACA TCTACAAAGA GACCTGAGCG GGTGGGGCAA AGAGGGGGTC CCAGGCAGAG 780
GGAGAAGCAA GTGCAAAGAC CTTCATAACC CAGGGGAGCG CTGAGACCAC CGACCAGCAG 840
CACCCCCACT TCTTCAAGCC ACCACTCCTC AGGGCCTCCC AGGGGTCCCC AGCCTGGAGC 900
ACCCCATGTG GTAGAGCTGG TAGGCTGGGG GACACTGGGG ACTGCTGTCC CACTTGGAGC 960
CTCGGGCTAC TCCGCCCAGG AGCAGCGATG TGGAACCTTG TTGGATTTTC ATGTTCCCAA 1020
ACATCCAGGA GACACACAGT TGTGAGTTTC CAGCCAGGCG ATCTCTAAGG CCAGAGCAGC 1080
CCTTGTGGGT GTCAGTGAGG AAGGGCAGAA AGACTCTGGC CTCAAGCTCA GCTCCCTGCT 1140
GCAGGGAGTT GAACGCCCCT TTGGTGAGTG GCTCTAGCTA AACAAACACG TGTTATCATC 1200
TGTCAATAGC GGCCACCTCC TTGCTGGCTG GGCTGCTGCT GGCTCAAAGC CCAGAGCAGC 1260
CCTTCCGGGG CACTGCCTGC CACAGCCAAC AGTCAGGGAA GGGCAGCTAC TGCCCTGGGT 1320
TCAAGCCCGG GCTACCCCTG CTCCTGCTCA CTGTGTGTCC CCAAGCAAGT CACTGTCCCT 1380
GCCTCTCTGT ACAGTGGGAG GCCTGGATCT CTCTGCTCTG GGAAGACACC CAGCCCTGGA 1440
ATGGTTGGGC CACACTTGGG GCTGGGGGCC AGGAGGAAGT TGGAGGGCTG GGCTGGGGCT 1500
GGGGCTGATT 1510
|
