| Tag | Content |
|---|
EnhancerAtlas ID | HS076-18412 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr14:90976220-90977410 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr14:90977366-90977381 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr5a2 | MA0505.1 | chr14:90976227-90976242 | GCTGGCCTTGAACTC | - | 8.25 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_05763 | chr14:90976040-90977241 | Brain_Cingulate_Gyrus | | SE_06526 | chr14:90975827-90992794 | Brain_Hippocampus_Middle | | SE_24186 | chr14:90976286-90976790 | Colon_Crypt_2 | | SE_24186 | chr14:90976934-90977383 | Colon_Crypt_2 | | SE_31992 | chr14:90976141-90977522 | Gastric | | SE_33611 | chr14:90974537-90981544 | H2171 | | SE_41893 | chr14:90976189-90977428 | LNCaP | | SE_47878 | chr14:90976875-90977447 | Pancreas | | SE_65518 | chr14:90974579-90981557 | Pancreatic_islets | | SE_66921 | chr14:90974537-90981544 | H2171 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I090507 | chr14 | 90974331 | 90977464 |
|
Enhancer Sequence | TGCCCAGGCT GGCCTTGAAC TCCTGACGTC AGGTGATCCA CCTGCCTCAA CCTCCCAAAG 60
TGCTGGGATT ACAGGAGTGA GCCACTGTGC CCGGCCAGCA CCCACATCCT TCAGGAGCCA 120
TGACAGAGGT GCAGAGAGGC AGGGCGGGGC TGGGGCTCAA AGCCCAGGCT CCAGGGCCAA 180
CCCAGGTTTG CACCCCAGCT TTGTGACCAA GGCCATATCT CTTCACCTCC CTGAGCCTCA 240
GTTTCCTACT CTGAAAGGGG GATAATAGCA CCCCTCCTGG GGCTGTTGTG AGGATCGAGG 300
AGGTAACATG TAGAAGGTGC TTTGCCTGGT GCTTGGCACA TAGTAGCAGA CAACAAACAG 360
TGACTGTCAT TATTGCATGT GACACAGTCA GACAGCCAGG CAAGGCACGA GTGGCCCTGT 420
GTTCCCATCT CTGGTGGCTC ACCCAGCTCT ACCGCCCCCT CCACCCCGCC TCACCTTTGG 480
TGGCGCACAG CCCAGTTGTT CTCGTTAGAC GATGCTGCTC TGCTCCCAAT GTGTCACTCA 540
CGTGAGCCAG CACACACCTC ATCCCTGCCC CCATCACTGT TTTGCTGGAA GAAACCCAGG 600
AGCCAGGGCC TCAGAGCCAG CTCCCCCTGT GCCCGCCTTC TTGGTCATGC AAATCAGAGT 660
GAGCTCTTCC CCTCTGCCTG GGCAGACTCC CGCTGACTCC CCCTTCATTC CTGTCCACTT 720
CTCCCCAAAC AAAACAGAAA GGAGGGCCCA GGAAAAGAAG GGGTATCAAA ATCTGGCTTT 780
TGAATCAGGC TCAGAATGAA TCAAGGTTTG GCCCCTGGAA GCAACATGAA CCCCCAGAGG 840
CTTGCGAGGT GCTGCTCTGC CCCTTACTAG CTTTGTGGCC TTGGGCAAGT CCCTTTACCT 900
CTTTGAGCTC CAGCTTTGTC ACCTCTGACA CAGGGACAGT AGTATAAGCC CTGGGGCACT 960
GTACACTCCT GCCTGGCTCT GAGCTGAGCC ATGTTGCCTC TCTGAGGCCA CTTTGATTTG 1020
GTCTGTCCTG TTCCTGGGTC CATAATTCCT GCCGCCTGCC CTCCCACACA GAAGTCCGAC 1080
AGGGTTACAG GCGTGAGCCC CTGCTCCCGG CTAGCACTTT GGGAGGCTGA GGCTGGTGGA 1140
TCACCTGAGG TCAGGAGTTC AAGACCAGCC TAGTCAACAC AGTGAAACAC 1190
|
