| Tag | Content |
|---|
EnhancerAtlas ID | HS180-23444 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr19:3338350-3339210 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr19:3339083-3339098 | AGAGGGCAAAGGGCA | + | 6.01 | | HNF4G | MA0484.1 | chr19:3339090-3339105 | AAAGGGCAAAGGCCA | + | 6.87 | | NR2C2 | MA0504.1 | chr19:3339083-3339098 | AGAGGGCAAAGGGCA | + | 6.56 | | NR2C2 | MA0504.1 | chr19:3339076-3339091 | GGAGGTCAGAGGGCA | + | 7.22 | | ZBTB18 | MA0698.1 | chr19:3338981-3338994 | CATCCAGATGTGT | + | 6.78 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_00151 | chr19:3334565-3339336 | Adipose_Nuclei | | SE_00856 | chr19:3338272-3339306 | Adrenal_Gland | | SE_24506 | chr19:3338388-3339150 | Colon_Crypt_2 | | SE_26532 | chr19:3338332-3339205 | Esophagus | | SE_31377 | chr19:3338315-3339284 | Gastric | | SE_42110 | chr19:3338284-3339233 | Lung | | SE_47457 | chr19:3338307-3339161 | Pancreas | | SE_50148 | chr19:3338298-3339225 | Sigmoid_Colon | | SE_54509 | chr19:3338321-3339308 | Stomach_Smooth_Muscle | | SE_65251 | chr19:3335050-3341018 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I003335 | chr19 | 3335221 | 3339206 |
|
Enhancer Sequence | AGCCTGGGCG ACAAAGTGAG ACTCAGTCTC AAAAAAAAAA AAAAAATTAA AATTAAAAAA 60
AAAAGTAAAG AAAGAATCCA GGCCCATTGC ACACATGGGA AACTGAAGTT GATGTTCCCA 120
AAGCAAGTCA GAGGCAGGGC TGGGAGCTGA GAAATCAGCT GGGAACCTCT CACCCTACAC 180
CTCCCTGGAG CCCAGTGGAG GGAGGCTGGG GGCAGGGGAC AGAGAACTGA GGTCATGGTG 240
CCAGGTCCCA AGGGGCCCAG GCTCACGTTC CTGCCTGATG GCTGCAAGCT CCCAAACATC 300
CCACTCTGAG CCTCTCCTTC CCTTCTCTGT ACGACAAGCC CCAGGGTGGC ACAGGGTGGG 360
CGGGGTGTTG GGGTGCCCGG CCACTCCCAG CCCTTTACAT AACCTGCGGC ACAGCAGGAA 420
ATCAAAGTGC CAACAACTGC CTCCTCAGTA ACCGACTTCC TGTCGTTACC CACCCACCTT 480
GGGCACCAGC TGCCTGCTCC CTACCTCCAG TGGCAGAGGG GTCCCATCCC TGACCCCAGG 540
GTTTCCTCCC CAAGGAAGGG CCCCCGTACC CTAGGCTGCT CCATCATGCG ACCCTGAGCC 600
AGTGTCCAGC CAGCTCTGGC CTCAGTTCCT CCATCCAGAT GTGTCCCTGG GCTGCCAGGA 660
CCGTCACCCT GCTCCTTTCG GCCACTGGCT GGGAGACTGC ATACTGGCTG CCCCAGACCT 720
GAGGCTGGAG GTCAGAGGGC AAAGGGCAAA GGCCAAGGAA TTCCCTTTTT TTTTTTTTTT 780
CTGTGACAGA GTCTCGCTCT GTTGTCCAGG CTGGAGTGCA GTGGCACTAT CTTGGCTCAC 840
TGCAACCTCA GCTCCCAGGT 860
|
