| Tag | Content |
|---|
EnhancerAtlas ID | HS098-46634 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr5:149561190-149562330 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZBTB18 | MA0698.1 | chr5:149561961-149561974 | CCACATCTGGAAG | - | 6.11 | | ZNF263 | MA0528.1 | chr5:149561257-149561278 | TCCTCCTTCCCTGCCTCCTTT | - | 7.23 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_01616 | chr5:149554754-149562929 | Aorta | | SE_23229 | chr5:149561073-149564125 | Colon_Crypt_1 | | SE_24021 | chr5:149561325-149562998 | Colon_Crypt_2 | | SE_25116 | chr5:149561262-149564991 | Colon_Crypt_3 | | SE_27738 | chr5:149556029-149569007 | Fetal_Intestine | | SE_28721 | chr5:149554463-149569333 | Fetal_Intestine_Large | | SE_50759 | chr5:149554619-149566880 | Sigmoid_Colon | | SE_52451 | chr5:149554733-149566936 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I150176 | chr5 | 149556223 | 149569018 |
|
Enhancer Sequence | TTTTCAGCAA GGCCTTCACG GCCCATTCTA TTTAAAATCA CAGACCACCT CCTCCCTAAA 60
TTCCCAGTCC TCCTTCCCTG CCTCCTTTTC TTCTGAAACA CTTATCAACT AGTGTATCAA 120
ATATTTTATG TTTATTTTTC TTTTCATCAT CTCCCTCCCC TAGAAGCTAA GCATCACGAG 180
GGCAGGGGTT TTATTTTGCT CAGTGCTGTA GCCCAGAGCT TGGCTCACAG CAGGAGCTCA 240
GTGAGGATCT GTGGGATGAG CTGCATCTCT CCTGCCCGGT GCCTGGACAC AGGGGGATGT 300
GTGGACGGCT TGGGCAGACC AGCCTCCGGC CTCTGGTGCA GGCCCAGCTC AGGGCTTGGT 360
ATCGTGAGCC AGAGCCTTTG AGGTAACTGG CAGGTCCTAG GGGTCCAGCA GCAGCCCCAG 420
TCCTCCCTGT CTGATGTTGA GGCCATCCCC AGGCATTCGG CAAGAACTAG GGAGCCCACA 480
CCTGGGACAG TTCCAGATTC TTTCTGCTTC CACCTCTACC TGTGGTGGCT CTTCCCTTCT 540
CTCTTCTCTT GCACAGGAGG AAGGAGCAGC TGCCATCTCA TTAGTCTTGA TCACCCTTGC 600
CTGCCCGATA TCCCCTCCGT GTCTCCAGCA TTCAAACCTA TCTGATATCT GACCACAGAG 660
TGGAGAGTTT GTTAAAAATG CAGATTCCAC CCCCAGGCTT TCTGACTAAC TGGTCAGGGA 720
TGCCCAGAAC CTGTGTTCTT CACAAGCTCC TGGAGAATGG CTGCTGTGCA GCCACATCTG 780
GAAGCTGCTG GTTTAAAGTT GTTGGAGCTG GCCTTCAGAA TAGGGCTCTG GGTCAGGAGA 840
CCTGGGCTGA AGCTGCAGCT CCGTCAGCAG CCTGCTGTGT AACCCTGAGC TGGTTGTTTT 900
GCCTACCTCA CTGCCTCCCT GATGGGCATG GGAGGAGTAC TTGCCTCCCA GACTGTGAGT 960
CTGTGGGTCT GAGTCTGGGA AATGACTGTT TCCCTTGAAC CTGGAGTGTA TGTCTCTCCC 1020
CACCTCAGGG TCCTACTTCA GGGAGCCTGG ATTGTCTTCC TCCTGGGGGT CCTGCCTGGG 1080
CCTTTTTTGT AGCCTCCTCC TCTCAACTCA CCTTCCTTCC CGGCTCCTTC TGCTTCTCAG 1140
|
