| Tag | Content |
|---|
EnhancerAtlas ID | HS073-01997 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr10:105559880-105561020 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr10:105560926-105560942 | CCTGGACTCTGACCCT | - | 6.34 | | NFYB | MA0502.1 | chr10:105560053-105560068 | CTGATTGGTCCAGAG | - | 6.26 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_23068 | chr10:105559615-105561362 | Colon_Crypt_1 | | SE_23830 | chr10:105560125-105561179 | Colon_Crypt_2 | | SE_25254 | chr10:105559667-105561274 | Colon_Crypt_3 | | SE_27893 | chr10:105559563-105561587 | Fetal_Intestine | | SE_28945 | chr10:105559571-105561640 | Fetal_Intestine_Large | | SE_35962 | chr10:105558509-105563629 | HMEC | | SE_50087 | chr10:105559637-105561453 | Sigmoid_Colon | | SE_64487 | chr10:105559428-105561443 | NHEK | | SE_68170 | chr10:105541167-105581099 | TC32 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I103798 | chr10 | 105558550 | 105563948 |
|
Enhancer Sequence | GCCTAAACCA GGCTCACAAC CCCGAGAGGA ATCTAGAACA TCTTGGCTCT ACCTGAAAGG 60
GCTGCTGCTC AACTCACACT GATTCTCCCT TCTCTAGTAC TTGCCTGTGA TCCGCAGAGG 120
TGGGCTCCCT AGTGGCCATG TCTGTGCTAA AAGACCCTCA ACTCCCAGCC ATACTGATTG 180
GTCCAGAGAG GGCATCTGAC CCAAGCCAGA CCAATCAAAA TCGTCCCTGG GATTTTTCAA 240
CTTGGAACTG GGAGTCAATT TCCCCTCTGT TGGGAGCCAA AAGATATAAA ATTCTAGAGC 300
TGCTGACAGC CATATTCCTC AGGGTGTGAG GTAACAGAAG CTGAGGGCAG TGCCAGAGGG 360
AAGCAGAGAC AAGACAGAGG GAGAGCAGAT CCTGGTTTCA GGCATTCCTG AAGCCTCTGC 420
CTCACTGCCC TTCTCACCAT GTGGTCGGCT GCACAAGCTT CCCTGGTCCC TCCTTCCAAT 480
CACATCTCCT TTGTGTCTAA GCCAGTGCAA TTGTAAAACT ATCACTTGCA ACCCAAAGAG 540
GCCTGACTAA CTTAGCTGGC ATCAAGGGGG GTGTCTGCAG GGGTAGCTGT GGGACCCATA 600
CTACCATTCC CTTGTGAACA TGCCTTTGTG TCTTAGAGAC ACACACCTAC CACGTACATG 660
TACAAACTGG GTGGCAAGTG CCTCATTCGG TCAGACAGAC ACCGTGGTAT GTATGCCTAG 720
TTTGTGCCTG TAGTTGAAAA AATTGCTTAT TTTCTGTTTC GGTCTTCCCT GAGTGTTTGC 780
TTTTCTTTGC CTGCAATGAT GCAGTGGCTT CTGTCTCACC CTGGATGTTT ATAGACACAC 840
GTCTGGTCAG GCACACAGCA CCTCCCACCA TCCTCCCGCC TCTTCACCAC AGTTTCCTAC 900
CCTGCAGGCA AGGGAGGGTG ACAAAGCGTT ACTGTTAAGA CCATCAGAGG AGGCCAACAA 960
AGTCCTGAGT GTCTGCCTGC AGTATGCAAG ATTGAGACGA GCCCAGCTCC ACCTTCCAGC 1020
TTCCCTCCTC TGTCCCTCTG CTCCCACCTG GACTCTGACC CTGACAGCTC TCTTGGGGGC 1080
TCCCTGGATA AGCGAGGGTA TGAGAGAGGC CAGCCCACCA GAGAGACTTG GGCCACTGTC 1140
|
