| Tag | Content |
|---|
EnhancerAtlas ID | HS180-46353 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr7:155743530-155745320 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr7:155744998-155745009 | CTTGAGTGCTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_34499 | chr7:155742769-155747459 | HCT-116 | | SE_58199 | chr7:155744127-155745492 | VACO_9m |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I155949 | chr7 | 155742313 | 155747521 |
|
Enhancer Sequence | TAAGCAGCAG TTTGTCCTGG ATGACAATCA TGGACAGGAT TGTTAAGGTC CTTGTGGGGA 60
AGGAGCTGGG CTAATTTCTC TACATGAATA CTCACTAAGT ACTCAGAAGA AAACCCTCTA 120
AAGTAGGATT CGTGAGTGCC CCATTTTGCT GACCTCAGGC AGAACAGGGG CACCAGGGTT 180
GGAACAGGGG GGTCTGATGG CAGAGGCCCC GTGCATCACG CTCACGTGAC TGCCCTTGCC 240
ATCAAAGAGC ATAGTCCACG GCCAGCAGAG TGAGCGTGGC CTAGGAAAGT TCTACCTACA 300
AACAGTGGGA GGAAAAGTGT GCTGGTCAAC CAGGATTCGG TAGAGGATGT TGGCTGGTGA 360
ACCCGTCTGC CCCGACTTCA GGAGCAGAAA TGATGTGGAG GACAGATTCT TTGAGGATAC 420
CTGAGGATCT GGCCAGGCCC TAGGGGAACA CTGAAAACAT GATTTTATTG TTCCGCAGGG 480
GTCAGAGCTA GAAGTGTTTT GTTTTCAGAT GAATCTGGAA CCTAAGCCCA TTCTGTAAGG 540
AATTGCCACT TAGTCCTACA CATTGAATGC AGAAAATTCT GATGGTTTAA TGCCTCTCAT 600
TTGGGATATC CGAAAACAAT TAGGGCTTAT CTGGATTACT GCAGCGAAAC AAAAACACTC 660
CGTGATGGCC AAGTGTGGAG CTGGGAGGAA CAAGAGGAAG GAGCCGGTGA TGGCTTTGTG 720
ACTCTTTCCC CAAATAACAT GCCCATGAAT CAGAGGCTCT GGGAGAAGGC TGCTGGTGAC 780
TCAAGGCCGG GTAACCAGCG AGCCCTGACC GTCCCTCCGT GCAGGACTCG ACTCGACAAG 840
GAATCCAGGG AATTGCTCCG ACAACATCAG GCCCGGACTC TTATTTGTTT TCATGTTTGA 900
GGGTGGATCT AAGCCCTGCA ACATCATCAA AACATTGTTT TAATGCAGGT GCCGGTGCCA 960
CACGTTAGAG GGCTTGTGCC TGCCAGCAGT GGAAAAGTAC CGCCTTGAGT CACCGCGGTG 1020
CTGAAGGTCA CTGGGCCTCC TTACGCAAGC CCTGGACCCG GCGCCCATGA ACTCGCTACC 1080
CTGGGCTGCG ATTGTTCTTT CTTTGGTTTC CCTGTGAGCC CCAGTGACAA ACCACCGGAA 1140
CCCAGAGTGA CTCACAGACA GTGGAGTGTC AGAGCCAAAA GGGGCCGTGT GAGCTTCCAA 1200
CTCGACCCAC AGCTCTGCCA GGAGAGGCAG CTGTGTCCAG AGGGGCAGGG AGACCTGCCT 1260
AGTGACCTGG CTGGTTGGTG ACACAGCCAG GCCTAAGAAT GGAGTCTTCT GGTGACAGTT 1320
TAGTGTGTTT GATCATGAGG AGAGCACTCA GACCCCACAT CCTCGCGGTT GTCTGTTCGT 1380
CTGGGACTCC GGGCCCCTGC CCACCTCCTC TGCTTCTCTC AGTGACACCA GGTGGTTTCT 1440
TTGCCTGGGA TCCCCACACC TCCATTCTCT TGAGTGCTTG GAGCTATGAC CTGTGAGGAT 1500
CCTTAGAACT CAAGACTACT GGATGGAGAG GGGAGTGAAG GGGGCCAGCG GAAGCCTGCA 1560
GGTGCCTGGC AGGTGGGTTT CCCCTTCACT GCCTCAAGCG ATGAGGTGGG GCTTCTGCGT 1620
CTTCAAGGAT AAGAATCCCT GTGGATGTCC TCTTGGGTCT GATGGCTTTA GGCTGCAAAG 1680
CCCTGAATTC CTCTTCTGAA ATAGGCAAAG ATGTGGGTGT GCTCACGTTG CCTTTTCTGA 1740
GCCAGCCCCC AAGCCCACAA GCTGAGCCTT CAGCTCTGCT AACGGTGCCT 1790
|
