| Tag | Content |
|---|
EnhancerAtlas ID | HS180-29483 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr20:14965490-14967780 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr20:14966958-14966973 | AGTTAATGAATAACC | + | 6.14 | | MSC | MA0665.1 | chr20:14966748-14966758 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr20:14966748-14966758 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr20:14966748-14966758 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr20:14966748-14966758 | AACAGCTGTT | - | 6.02 | | ZNF263 | MA0528.1 | chr20:14966456-14966477 | GGGGCAGGGAAGGAAGGGAAG | + | 6.06 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35330 | chr20:14963816-14968794 | HepG2 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH20I014984 | chr20 | 14965084 | 14968669 |
|
Enhancer Sequence | GTACTCTGCT CACCCTGCTC CACTCCACCT CTCAGGCTTT TGGTTTTATC AGATTGTGTC 60
TATAACAAAG CCAGATAAAA GTGACAAAGA AGTGCAGTTC AAGGTTCTGC TGTCCTTCCC 120
TTGTCTCTGG GAGTTAGCAA GTCACCTTTA AATGAGAAAA CAGTGTGACC TTACGTACTT 180
CACACGGCCA TTCTGAGACA AAGTTGGAGA AGTGTCATGC ATCACTGCAC TCTTCTAAGG 240
GGTGGAAGGA ATCAAGCATA TTCCAGACCT AGGAGGGATT TCTTAGGAAT TCACACTGAT 300
GTAATTTCAA AACTCCCAAG ACAGCCACCA CTTGTCTGGC ATTAGCTAAC CTATGACACT 360
TCACTCAATT GCATTTTGAG CTCCTGACTT AGTTCATTCA GTAACGTTTT TGCCCCAGGA 420
TGCCAAAGCA AACACTGGTC CTGAACTTTG CCTCTTGAAC TACATTCTTC ACCATGATGC 480
CCTTCCAAAT TCCCTATAGA TGTTTTCACT ACTGGTGTGT ACAGGAAGGA AGTTCACTTT 540
GACTAATAAC CAACTCTGTT ATTTCTAGTG GAGTGATCAT TTGTCTCTTC TGTCCATTGG 600
CCTCCCTTTG ATTCAAGCAG TGGGGTGTGT AGAGGAAGCT CTGCATCCAC TTGACAAGCC 660
TTTTAGGTCC CAACAGCAGT GGACTCCTTA TCAGGGCTAC TCATAAAAGG CTAACCTTCC 720
AAAGGAAACT TGTCAGGGCT CAGCTGTTGG CAAGATGGAT TAACAAGTGC TTCCAGCTAA 780
TGGAGTAGAC ATTGGTGACT TAATGAGGGT AGTTTGAAAT CTTAGCTGTA TTCTCTTATT 840
CTTTTTTTTT TTTTTTTTGA GGATGATAAA TGAGTTTAGT TCTTTCTTAG CTAAGAAATG 900
CCAATGATTT ATTTTTATTA TTCTTATTTT TATTTTTTAT TTTTTAGAGA TATGGGGCCA 960
GGGTCGGGGG CAGGGAAGGA AGGGAAGTCT CACTAGGTTG GCCAGAATGG TCTCAAACTC 1020
CTGGCCTCAA ACAATCTTTT CACCTGGTCC TTCCAAAGTG CTGGGATTAC AGGTGTGAGC 1080
CACCTTGCCC TGCAGAAATA CCAATTATTA AAAACTCAGA GGTTGTAGTG CAACATATTT 1140
GGGAGTGGTC ACACCCCATG GCCTTTGATT TTAGTCTGAA GATTGAAAAT AACCTTTGGA 1200
TTTTACCTTG ACAAGGAAGT TGTTCCTCAG TGGACACAGA CATCATAGTT GGCATAGAAA 1260
CAGCTGTTGG GTTATTCCTG GGCCATTGAA GACATGGCAC CTGGCCCAGT CTGAATGGTT 1320
GTTCTCTCCT GGTTGCTTGT TTAAATAAAG GTTAAGCAAA AATTCTTTTT TGGTTTTGAT 1380
TTCAGGAAGA AATAAGGGAG TGACTGCAAT GTTATCTGAA AATGAGCATT TCCTGTTTCC 1440
TCAGGCATTT CTTTATGACC CCCATTAAAG TTAATGAATA ACCAAGTGTC TGACACAGTT 1500
GAGCGTAATA TGCCTCACCT AAGGTTCCCG GTGGCTGCAC ATTTTTGTGG GAAATGACCT 1560
TCAGTTCCTG CAGATCCATT ATTAGGCAAT CTCTTAGTTA TAGACTTTAT CTTCCCAAAA 1620
CATTCAAATC ACATATTAGC CAAATCACTT AGATACCGTC CTAAGTGCTG GAACTCTTTA 1680
AGTCTTGTTA GCAGAAAAGG CTAAAGTTTA GGTAAATAAG CAGATCTGTT CCACAAATGA 1740
TTCCTCACCT TAGGTATTTA TGAAAAAGCT CTGATAAACT TTTGAAAGCA GAAAAAGACG 1800
TTAAAAAATC TTACTGTGAG CCTGAAAACA TAAACATAAA TCAGCTAAAA GATAATTTGC 1860
CTTAATAGGT AGTGGGCGAT GGGGGAGGAG AGTGATCAGG GCTCACCCTG GCAAAATTGT 1920
CTCTGCCGGA TGTTTCAGGT TCGCCTTCTC TCCCCGTCAC CTCCTCAGAA TCTTAGGAGA 1980
CCACATAGGA TCAATCCTTG TTCAAAGGCA AAGGCAAAAA AAGTATGACT GCAAATATGT 2040
GAAGTACGAT TTGGCACGGA GTTCATTTTG GGACCCTAAG TCCTCTAGGC GGTACAGCTA 2100
TATATTGCAA TGGACTGAGT GTTTGACACA CTTGCCCAGA ACTCCTGCAT ACAAATGAGG 2160
AGTGGCATCC TTAACCTCAG GCAGTTAAAT GTTCCATTCC CCTGAAACTA CCATTTTCCA 2220
AAGAGCTTTG GAATTGTCTT AGGGCCTATT TAAATGCCAT AGGAAAAAAG TTAATTTCAT 2280
TTCTTTTTAT 2290
|
