| Tag | Content |
|---|
EnhancerAtlas ID | HS102-01486 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr1:116901690-116902970 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:116902817-116902829 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr1:116902821-116902833 | GTTTGTTTGTTT | + | 6.32 | | POU2F2 | MA0507.1 | chr1:116902354-116902367 | ATATGCAAATAAG | - | 6.57 | | Pou2f3 | MA0627.1 | chr1:116902352-116902368 | TCATATGCAAATAAGC | + | 6.2 | | Stat6 | MA0520.1 | chr1:116902230-116902245 | TTTTCTCTGGAAATC | - | 6.39 | | TCF7L2 | MA0523.1 | chr1:116902098-116902112 | AGACATCAAAGAAA | + | 6.44 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_28411 | chr1:116901305-116905150 | Fetal_Intestine | | SE_29219 | chr1:116901136-116905351 | Fetal_Intestine_Large | | SE_68278 | chr1:116891785-116921287 | TC32 | | SE_68497 | chr1:116891900-116921072 | TC71 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I116358 | chr1 | 116901137 | 116905351 |
|
Enhancer Sequence | ACCTGAATAC TAAATTTCAT ATTACTTTCC TAAAGACTTA GTTCAGTGCT ATATACACAT 60
AGACAGGAGA CAGCTATAGC CTGAGAGGTA CACAGCTGAA CTGAAATCAA AAGACTTGAG 120
TGAAATCTTT TCTGTACCTC TGACTCTGAG CCAGGCCATA ATCCCTCTGA ATCTCAGCTT 180
CCTCATTCCT AACACATGAT TAATGAGGTT GTCACAAAAA TTCAAAGAGA AAATAGATTT 240
ATCATGCACA GAATTTGACA TGTGGAACCA ATGCCCTGCT ATTTGAATCT AAAGGCAAGA 300
AATGCTTAAA TCAGCTACAG CCAAAGAAGA GTAATGGCAG GAAAGCATTA TAACTTCAAA 360
AACTGTTTTC CAGTGGTTAA ACATTATTAC CAAAGTTACT TCAGTCAAAG ACATCAAAGA 420
AAATTTATAA TCTTGTCTCC AGATAACATG TACGTTCATC AGTTGCGGCT GAAAAGAAAA 480
GTTCCCACCA CCCTGAAGAC CATCACTGGC CCTGGACTTC CTAAAGCAGC CCAAGAAACA 540
TTTTCTCTGG AAATCTGGTC TTTTGTGTGA GAGTGAAAGC TACTGTGGGT GTTGCAATAC 600
TTTTCCTCTG CAAAGAGATG ATTTTAGCAG AATCCCAAAT AGCACAATAG AATTATCTGT 660
ATTCATATGC AAATAAGCAC ATTTTAAAAT ATAGTTGAAA CAAATAGGAA TCCCTTTTAT 720
TTCCAATCTC ATCTCATGTT TCCATAATGG AGATACTGGG ATTAAAGATG ATTATAAAGT 780
GAATGTAGAT TTGTGAGAAG TAGGCTATCA TGAGAAATGC TGGGGGTGTG GAGCCCTTGC 840
AAACACTTCC CAGGATCCGA AAGCAGAAAG GATAGAGGAA AGGCATTAGA CTAAGCCATG 900
AGAGTCATGG CAGGAAGAGG ATTTGAAGAA TGAAGCTTGC AGCACTCTTG TTGAAAGACT 960
GAAGGTAAAT GACTGGGCAC CTCTTCAATA GCAGCCCTCA CTGACCACAC TAACAAAAAT 1020
ATTCCCCACA CAGCCCCACC TCCTCCCTAG TTACTCTATC ATACCACCAC CACCTGCTTC 1080
ATGGTTCTCT TTGAGCTGAT AACTATGTTG TATTATCTTG CTTATTTGTT TGTTTGTTTG 1140
TTTCCTTTGC TGTTATTTAT TTCTTCCACT AGGCTGGAAA CTCTGGAGGA ACAGGGACAT 1200
GGCCTATCTT GTTCATGTGC CTCGATCAGT GCTAAGCACA GAATGGACAT TCAATAAATG 1260
CTATTTGAAT GCAAAAAGGG 1280
|
