| Tag | Content |
|---|
EnhancerAtlas ID | HS180-00119 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:3271720-3272870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:3272603-3272618 | TGGACTTTGAACCCA | - | 6.99 | | Hnf4a | MA0114.3 | chr1:3272601-3272617 | GATGGACTTTGAACCC | - | 7.25 | | Klf1 | MA0493.1 | chr1:3271878-3271889 | GGCCACACCCA | + | 6.62 | | RREB1 | MA0073.1 | chr1:3272461-3272481 | CCCCCAAACACCCCCCAAAC | + | 8.08 | | ZNF263 | MA0528.1 | chr1:3271795-3271816 | GCAGGAGGGGGAGGGAGAGGA | + | 6.13 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_01548 | chr1:3261400-3275654 | Aorta | | SE_28099 | chr1:3269171-3273832 | Fetal_Intestine | | SE_40807 | chr1:3270924-3272227 | Left_Ventricle | | SE_49549 | chr1:3271029-3271865 | Right_Ventricle | | SE_65787 | chr1:3270885-3271876 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I003345 | chr1 | 3262093 | 3272904 |
|
Enhancer Sequence | CAGACCTGAA GGTGTGCCGG GGAGCTCCGA GCTCCAGGCT CTGCAGCTGC ATCTGGGGCC 60
AGGGCCTGAG GCCTGGCAGG AGGGGGAGGG AGAGGAGTAC AGAGTGGAGG CCTCCGGGGT 120
ATCAGGTACA AAGTGAGAAG GGCCTAATGC AGGGAGATGG CCACACCCAC CCACCCACCA 180
TCTGACCTCA CGAATTAATT GCGCCTGCTC TTCCAACACA GCTTCTCTTT CCATTTCTTC 240
AGCCTGGCGG GGGGCTTGGC CTCCATTTTC CTGTCTCCCA GGCAAGGGGT TGAACTAAAC 300
AGTCCCTACT GGTTGGTGCC ACCCTGGGGA GCTAGGTCTC AGGGGCTCTG CTGGTTGCAG 360
CTCTTGTTTG AAGGAGGGAG TTTTGCAGGG ACCCTGACGC TACAGCCAGG CGTGCCCAAG 420
AACAATAAAA ACAAGGGCAG CATCCGCTCG ACGGTGGGTG CTCTCCTGCT GGGGGGACCG 480
CTATCCTGGC CACACACCTT CACTCTTGTG GCCCCGGACC CTCAGCACCT CTCAGACCAC 540
ACAGATGAGA AACTGGGGCC GGGAGAAGTG CAGCCGCCAC CCTGAGGGTC TGAACCGTTC 600
AGGGGTTGCG GTCCACTTGC CCCCAAGACA GTGCACTGCC ATGTGGGGGT ACACAAGGCT 660
GCTGGCTCAG AGGCCAGTCC TGCCCGCCCA GCCTGTGTGT CTGTGAAAAT CAGGGTGCCC 720
TGCAGATCTC AGACCCTTCC TCCCCCAAAC ACCCCCCAAA CACCCTGGCC GTAAGATCTG 780
AGGTGAATGT GAGCAAAGAC GCCTTTCCCC ACTCCTCTGG GCACATCCTG ATGAGTGGCC 840
CGTTGGTGAC AAGTTGACAG AGGGGCCCCT CCGTGACAGG TGATGGACTT TGAACCCAGT 900
GCAGCTTTCA GGGCCCAAGA CCTTTCATGT TCTTCTGGAA ACGGTGCCAT TGGCTTTTCC 960
CATGACTCCC ACGAGGGCGT TAGCAGAACC TCCCTCATCT TGAGCAAATC ACGTCCTTTC 1020
GCACACCAGC ACGCGGGCAC AGATGAATCA CGCAGGGGGC TTGAGCAGGC CGACGTGTCT 1080
GGTGTTTGTG GAATTGTTCC AAAGCCCCCC CCAGCCCCCC TGCGCCAAGC CACCATCTCT 1140
AAAGGTGACA 1150
|
