| Tag | Content |
|---|
EnhancerAtlas ID | HS048-22328 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:234310600-234311840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr2:234310813-234310825 | TCCTGTTTACAT | - | 6.02 | | Foxo1 | MA0480.1 | chr2:234310813-234310824 | TCCTGTTTACA | + | 6.62 | | Nr5a2 | MA0505.1 | chr2:234311057-234311072 | GAGCTCAAGGCCATG | + | 6.49 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_10983 | chr2:234303271-234312272 | CD20 | | SE_24361 | chr2:234310970-234311861 | Colon_Crypt_2 | | SE_31410 | chr2:234310510-234311845 | Gastric | | SE_50646 | chr2:234310868-234312043 | Sigmoid_Colon | | SE_52992 | chr2:234310596-234312030 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I233402 | chr2 | 234311133 | 234311172 |
|
Enhancer Sequence | CTATAAACCA TCGAGGGGCC CCTCGTTTCT TACCTAATGA AGTTCAGGGT CTGGTCCTCA 60
TGTGCCCTCC CAGCCTGGCC TCTCCCCAGC CAAGCCCAGT GCTTCTTAGG GAGCTCCCTG 120
TGTGTACGGG TCACCTGCTG GCCCTGGTCT CTGGGGGTCT GTTTCCCCAA ATTCTCCCCA 180
CCGACCCTGT CCGTTTCCTC CTCAGGGAAG CCTTCCTGTT TACATGGTGC TCAGGAAACT 240
GCCATATGCT TCTGTGGGAC TGTGGTTCTC AAACTTGGCC ATGCCCGAGC ACCTTTTGGA 300
ACTTTCCCCA GAAGTTTGCA AGTGGGTGCT TTTTCAAAGC TTTCCAAAAT CTTAGGGTAC 360
AACCACTTTG GGACCCCCTT CTTGAGGGTA CTTTGTGTCA CTCATGTGAT GCTACATTAG 420
CACAAGCTCC CTAGTAATGT GTACTTGGCC ACACCTTGAG CTCAAGGCCA TGGAGTGTCT 480
TGGCAGCTTA GGGTCCCCAG TGCTCTGCCC TTTGGGGTGA CTATGTGTAT GAATATGAGC 540
TGGAAGAAGC AGGTTCTGTT GCTTCTTTTT GTTAGCACAA CAGAGAGAAT GTTGACTCAC 600
CCCTTCCTTG GCAAGCCCCG CTGAAGAGGT GCTCACTATT GTGGACCCCT CTGTGGGCCA 660
GGCTCCCCCT TTTACAATTT CCCAGCTCAT GTCCGGCCGG CAGCTTGGGG ACAAGGTTAG 720
CCCCTGTGCT CTGTGTGTGC GCTTTTAGCG AGTTTGCCAG CTGGAAAACT TGTTTATCCC 780
AGAGAATGGA GGAGTCATTT GACAAGTAAG GCATTACCCT GGCCACCTAA TTTCAAATCA 840
GTTGGAAAAG ATGCAAGTTT TAGAACTTGT TATTCCTTAT TTGAACTATC CTGTATCACG 900
GCAAACTGTC TACTGAGTGC CTGAGGGTGT ACGGGGTAGG TAAGTGTGTT CCCTACTCTG 960
GGAGACTTCT AACAGTATAT AAAGAAGTAG TTCTAGTGCC CTGTCATAAG TAGAGTGGAA 1020
GAAGGTACAA AGTACAGTTA GAGTGGTGGT GGTTAGCCTT GGGAGGGGAG GTAAGCTTCT 1080
CTGAGGAGCG GCATGAGAGC TGGATGTGGG GACGGGTCCC TTTTGCAGAG AGGACTGGGG 1140
AAGAGTCAGG GAGTCGGGGA CATCCAGGAA ATAGGTGGTA GGAGTGTCTG TTCATGTGAC 1200
ACACTAGCAG TGCCTGCTTT CCAGGTACAA GTCCTCCTGT 1240
|
