| Tag | Content |
|---|
EnhancerAtlas ID | HS048-27595 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr4:39470390-39471630 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr4:39471222-39471241 | TTACCAGCAGAGGGCAGCT | + | 6.52 | | HSF1 | MA0486.2 | chr4:39471169-39471182 | GAAAATTCCAGAA | - | 6.17 | | SPI1 | MA0080.4 | chr4:39471333-39471347 | TACTTCTGCTTTTT | - | 6.45 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35802 | chr4:39470781-39472158 | HepG2 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I039468 | chr4 | 39470392 | 39471920 |
|
Enhancer Sequence | GGCTGAGGCA GGAGAATTGC TTGAACCCGG GAGGCGAAGG TTGCGGTGAG CCGAGATAGT 60
GCCATGGTAC TCCATCCTGG GCGACAGCAA AACTTTGTCT CAAAAAAAAA AAAAAAGAAA 120
AAAACTCATA TCATTCAGAT GTACTTTTTA AAAAAAGTAG ACACTATGCT TTCTTATTCC 180
TAATAATTTC AGTAATTAAG ACTAATCATT GGCAAGTAAC ACTGATGTAA GAAAAAAAGT 240
AAGGATTGTT ATCCACATCC ATTCAAATTT TAGAAAAATG AACATTTTAA GCTTCGGGCA 300
AGAGTAATAT CATTTTTTTC TTTAATTTTA GCATTTAGCA GTGATTTTAT TAGCTTCTAC 360
ATATGATCTG TGTCATAGAG CCTGAAAGAA GTTACAGTAA ACAATAACCA CCATTTTCAC 420
TAAATCATAA ACAGTAGAGA CCATAACTTA ATTTCAGTGG AGAAATTCTG TTAAAAAGTG 480
ATTTCTATAA TGTCAGTTTC AGTTACTTTT AAGTTCATAA ATTTGTTTCT TCTCTTTCCT 540
GTTAACTAGT CTCCAATGAA AAACAATTAC AGAAAATAAA GCTGCATTAG AATTGAAATG 600
AAATCCAGTT TAACATCAGA AGCTTTCTGG CCTTTTGGCT TAAAGGATAA GTCATTTAAG 660
CCATGGTGGT TTGGCCATTG TTGAAGTCTA GGACACAGCC TGTTCCAACC TCATCATGAT 720
ACCACCACCA GTGGGTGCCA GTTTCCCTGG TTTCACTTAA AAACATGATC CTTTCCAGTG 780
AAAATTCCAG AATCATGCAT TTCTTTACCT AATATGTGGC AGTGTTGTAT ACTTACCAGC 840
AGAGGGCAGC TTAGTCTTCA GAAAAGAAAT GAACTTGAAA GTTTCAACCC TCTGACATGT 900
GGGTTCAGCT TATTTTTTTC TTTGTTCAGT ATGGAGACTC TCTTACTTCT GCTTTTTTTC 960
CTTTCTCTTC TAATTTTTCG CTTCAGAATT CTGGTTTCTC AATGCATAAA CTGAAGTAAT 1020
TTCTTCCATT CTACTTTTCT CTGCCCCAGG CTTGAGATAG AACTAGGGAG CCCAGTGAGG 1080
CCTTTTCTTT CCTAAATTAA CAGGCATCTG TGCATAAATG CTACCTTTGA ACTATGTGAT 1140
TTAAGATAAT GTGCAGAATG TACTTCTCTG GTCTTTCAGG TTGCTTGCAT AACTATGTAC 1200
TTGGTTGAAC TTGTAATTCT TGCTGACAAC AGTCCTGCTG 1240
|
