| Tag | Content |
|---|
EnhancerAtlas ID | HS158-09754 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr11:16981220-16982630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr11:16982009-16982029 | ACCCCACCCACCTCCACCGC | + | 6.25 | | RREB1 | MA0073.1 | chr11:16982005-16982025 | ACACACCCCACCCACCTCCA | + | 6.35 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_23209 | chr11:16981196-16982534 | Colon_Crypt_1 | | SE_24588 | chr11:16981290-16981865 | Colon_Crypt_2 | | SE_24588 | chr11:16981917-16982251 | Colon_Crypt_2 | | SE_27642 | chr11:16979996-16982922 | Fetal_Intestine | | SE_28618 | chr11:16980131-16982867 | Fetal_Intestine_Large | | SE_31464 | chr11:16980331-16983414 | Gastric | | SE_52571 | chr11:16980281-16982493 | Small_Intestine | | SE_67445 | chr11:16979595-16986500 | MM1S |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I016958 | chr11 | 16980143 | 16982809 |
|
Enhancer Sequence | ATTGAAACCA CCTTGATAGA AAGGCTGGAG CAACAAAAGG CCTACTCAGT TGAAATCTAA 60
TCTGTGTTAA TTAACGCCCC TGAGAATGAA AACACTTCTT TATCAGTGTG TGGTTCCTGG 120
CTAAAGCTCT CCCATAAAAC CTGCTTCTGG AGGGGGTTGC GGGCTCCCCT CAGCAGCCCT 180
GGAGGACTGT ACCTACTTCC CCCCAGGTAC CAGGAGGCAG GGCCTGCCTC CCCGGGCCAA 240
GCCCAACTGA AGGAGCCCAG GTAAGGCTGC AGGATTGTCA GAGCTAAAAC CTACTGCCCC 300
CCAAGGGATC TACTGACAGA CCAGAAGATG TGCAGTGGCA GGTCCTGCCC CCCAACCTCA 360
CTCCTGTGCC CTCCTTTCGC TGGCCCAGGC TGTGTGTGTG CACACACGCC TCCACATCCA 420
CACAGGTTCT CACGCCCTGC TCTGCTCCGG CTTCACTCTC CACTTTAGGC CACGTTCCTT 480
TCAGGGGCCC CCTTCACTCC CGGACGCTGA CCCTGTTCCC TTTTGTCCAG AATGCATAGC 540
ACCCCCACCA GCTCCCCTGC TTCCACAGCC AGGACCCAAG TCCAGGACTC AAGTCCCACC 600
CGCCCTGGAG AAACATGCTA CTGTTCCCAA GTGCCTGGCA CCCAGAGCAG GAGGCATGGG 660
CCCCAGAAGC CTGAGCTGGG CCAGGAAGTG GGAATGAGAT AAGCCATCTA GATTCCAAAT 720
TCTCCCTGTA TTTACTCAAA CGTTGCCTGA GCTCTGAGTT GGGGGGCAGG GGAAGAAGGA 780
GACATACACA CCCCACCCAC CTCCACCGCC ATGGGCAGAA ACAAGCACTG CAGAAGGTCA 840
CAGATGAGGC AAGCGTCGCC CTAGGGGTTC TAGGAAGGCC CTTCCCTCAT CTGTGACCTT 900
CCCATGTGAA GTATCCAGCA CAGAGTCCCC TGCAACAGTA GGTGCTAACT ATAAACAGGT 960
GACTGCAGGG CAAAGAGGAG AAAGGGGAGC CACAGCCCAA GGTGATACTC AACCCCTGGG 1020
TCCCTGCTCA GCCACAGGAG AGGTGCTTAA ATAATAAATA ACAAACAACA ACGACTGTGT 1080
AACAGCTACA CCCCATGGCT GAGGCCTCCC AATGCCTTAG GGTGGGAACA CTGCCATGAG 1140
GGACCCTACC TTCACCCCTA ACAGACAGAT GGGGACACCG AGGCACACAG GGGGCTGGCC 1200
TAGGCTGGGA AAGCAGCTCT CACTCCAGTT ACCCACAACT CCTTGAACCC AAGCTCATCC 1260
TGAAACTTCC AGCTTCGTTT CACCACGTCA GCCCCTGCCT GTCTTTCCTC CACAACAAGA 1320
GACCCAGCCA GCAAGTCCCC CTCCACCCCA CTCAAGGAAG GCCACTGCCC CGTGCCCAAG 1380
AGGGGGTCTC TGTCTAAAAA GCTTGATTCT 1410
|
