| Tag | Content |
|---|
EnhancerAtlas ID | HS101-39150 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr7:366140-368140 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr7:366943-366958 | AATTAATCAGTAACA | + | 6.19 | | NFYA | MA0060.3 | chr7:367013-367024 | TCTGATTGGCC | - | 6.02 | | NFYB | MA0502.1 | chr7:367014-367029 | CTGATTGGCCCATGC | - | 7 | | SREBF1 | MA0595.1 | chr7:368022-368032 | GTGGGGTGAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_24141 | chr7:366635-366954 | Colon_Crypt_2 | | SE_24141 | chr7:366971-368304 | Colon_Crypt_2 | | SE_28128 | chr7:365975-368406 | Fetal_Intestine | | SE_29038 | chr7:366018-368426 | Fetal_Intestine_Large | | SE_31770 | chr7:366016-368071 | Gastric | | SE_47737 | chr7:366083-366963 | Pancreas | | SE_47737 | chr7:366969-367993 | Pancreas | | SE_65801 | chr7:365498-369063 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I000326 | chr7 | 366189 | 368310 |
|
Enhancer Sequence | GCAGTTGATT TGTCTTTTCT GTTCCATGCA GCCCATTGCT TCCTAACTCA TTTCTTCCCC 60
TCATCTGCAC CTGTAGCTGG TTTCTGTCCT TGTGCTGTTT TCCTGGATAC CCCAGGCACT 120
GCGTGGCCTG CTGTCTGTGT GTCCAGCCCA CTCACTCCCT GTCCTTCCCA CCAGCTAGCT 180
GGCACTTATG GCCAAGTTTC CAGAGACCCA CAGAGGTGGC CACTGCTCAG AAACAAGGCT 240
TGTTCCTGGG GCGGTTGAGA CAGAGATGGG CGCTGGTCCC CGTGTGAAGC TGTGGATACA 300
CCAGTGGGCA GCTGTCATGT TCAGACCCAG GACCCAGTAC CCGGCGTGGC CGCCCTGGCT 360
GTCGTCACGG CTTCTTTTAA GGGGGCAGAG CAGATTGGCA CAGATGTCAG GGGCCCATGC 420
ATGTCCCTTG GCCTGGGGGA CTTAGAAGTT TTCTCTGTAT TTGGTTTCCC CTCTCTCAGC 480
ACTTTCTAAT ATACAGACTA AAACCCCAAC TCACTGGGAG GCCAGGATAT CAACGGGCTG 540
GAGATTTATG AGGGAAGAGC CGGGTCCCAC CAGCAGGCAC TAATAGCTCC CTAATTCCTG 600
TCATTAGTTA ACGAGAGCCC CTAGGTTCTC TCTACACAGC AGCTCGAATG TAATTACCAG 660
CTGGGAGTGC TGGGCACACA GGCCTTGTGT CCTGTGTTTT GCAAAATTCC CTGAAATGCA 720
CTTCATGATT CTGGAAGCTT CAGTCGGCTT GCAATTACAA GTAGCCCTTA TTAAAAATCC 780
ATGCAGCCTC CCACATCAAA CAAAATTAAT CAGTAACAAG CTGTAAGGCT ATTAGGTCAT 840
TTCCCAACAC AGAGCAACTC AGGAGTGGCC CTATCTGATT GGCCCATGCA CGGAGGCAGG 900
AATTCTCCCA TGTTTCTCTG AATGCCGTGA GCCTGACATG AGATGTTTGT CTTTGCTTGA 960
ATTACGTTTG GGTGTTATTC TGCTGAATCT ATTCCCATTG GCCTGGCAGG CTCACTTTGC 1020
AGCGCACACA CCACCAAGAT GGTCATCTCA TTTTGGCCAA GAGCATGAGG AAACATGTGG 1080
TCCCTGTTAG GGGAGGACCT CAGGTGTGGC CCTCCTCACC TCAGCCAGGG GGCCGAGCAG 1140
GAGCTGTGAG ACAGGGTCCT GCCCAGTCTC CCCGCACCCA CCTTGCCCTT TGCATGCAGC 1200
TCTGGCGCAC AGGCAGCCAG GATGAGTCCT TTCAGCAGGC GCTTTGAATC TCATAGCCAC 1260
TGTCCTTCCC GTCCACCTGG CCCATCCCGG CCCGCCAGGC ACCTGCACTG TCGGGTCTCT 1320
GCCGGCCTCT ATGCCTGGCT CTTCACTCTG CCCACTGGCT GCCCCATGGT GGCCACAGCG 1380
ACATCTCCCA GCCCAGCCAG GGGCTCTTCT TATGAGAGAC TGATAGGAAG GTGGGGTCCA 1440
GGCCCCTGCC CTGGCCTCCA GGGTGGGCTT GTGGCAACGG CAGAAACCAT CTGCGTGACT 1500
TGTGGGGTCT GAAGTCACGG GAGGCGTCGG TGTCAGCCTG GTCTCTGGGA ACAGGCACGT 1560
GCAACCCCGA GCTGTCCAGT TAGCCGTCTG GATGCTCCGA GGCCACCGTG CTGTGAAACT 1620
ATCGCACGTG GAGAAGCCCT GAGACCATGG GGAGAGAGAG AGATGCCCGC CTGCCCGCCA 1680
CGGCTCCCAG GCAGAGCCTT GGCTCATTCT AATCTCTCTG CCTGGACCTC TCCTCCCCGC 1740
TGTCTCCACG CGGCCGGCCC CTTTGCATTC TTCACCTCTC TGCTCAGATG CCACCTCCCC 1800
TTCATATCAC CCTCTGTGAG GGAAACGCCG GCCCCATGGT CCCCCACAAC TCCCTCCCTC 1860
AATGTCCCGT TCATTCCCTC TTGTGGGGTG ATGCTGGTCA CAATTCACGC TCCCATATTC 1920
ACTTGCTGAC TTGGGTATTG TCTGCTTCCC CAGCCAGAAC ATGGTTTCCC ACACCTGCCT 1980
GGTTCTCTGT TGCTTGCCCG 2000
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