| Tag | Content |
|---|
EnhancerAtlas ID | HS145-09526 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr16:88575360-88577350 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr16:88575824-88575839 | TGGACTTTGCACTCC | - | 6.97 | | Hnf4a | MA0114.3 | chr16:88575822-88575838 | GCTGGACTTTGCACTC | - | 6.3 | | KLF5 | MA0599.1 | chr16:88575392-88575402 | GCCCCGCCCC | + | 6.02 | | SP2 | MA0516.2 | chr16:88577057-88577074 | CTAGGTCCCGCCCCCTC | + | 7.08 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_27721 | chr16:88568463-88577886 | Fetal_Intestine | | SE_28915 | chr16:88574572-88577717 | Fetal_Intestine_Large | | SE_31396 | chr16:88568498-88581390 | Gastric | | SE_47499 | chr16:88574692-88576861 | Pancreas | | SE_52490 | chr16:88568748-88577075 | Small_Intestine | | SE_65338 | chr16:88568727-88580704 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I088502 | chr16 | 88568787 | 88577799 |
|
Enhancer Sequence | CGGCGCGTCA TCGTGGACAG AGGGGCCGGC TTGCCCCGCC CCACGCAGCT GACCCCTGGC 60
CACCCCGGTC TGCCTCCCGT GTGACCCTGG GGAGCCGCTC GCCCCTCTGG CCTCGGTTTC 120
TGTGTCTGTA CAGGATGTGT TGGAAGCTGG TGTTCTCGGG GCCCACGTGG TCTGTGCACC 180
AGCCTCACCG CCAGTCCGCT GACCCACAGA GGCTTCCAGA ACCCCGTCAG CCTGGGGTTT 240
TTCCTTCCCT CCCCCTCACT CCTTTTTCTT TCCTTTTTTG TGACTTTTAT CAAAAGCAAA 300
CAGCATGATC CCTGAGACAG GGCCGCTCCC AACAAAGCTG GACCCAGCTG GCCTATGGGA 360
GCCACAGGGC GGGGCCGGGC GGAGCGATGG GGCCGATTAG ATAAGTGGGT GCTGGGGTGA 420
CCCCACGGTG GGCACCAACC ACAGAGCCCA CCATCTGGGG TGGCTGGACT TTGCACTCCC 480
GAGACTACCA GCCATTAGGC ACACAGGGAG GCTGGCCCCT GGAAGGCGGG AAGGCCAGCT 540
GTGTGCAGGA GGGGCCCCGG TTCCCGGACG TCCGCAGACT CACAGGGTGA CGCCTTCACC 600
TGCCTCCTCA AGTCAGAGCT GTGAGCCAGC CTGCCAGGGC CAGGGCTCAG GTGGAGAAAC 660
AGGCCTGGGG AGGCGGGCGG CTGAGCAGAG TGGGTTCAGG AGCAGGTGGA GAAACAGGCC 720
CAGGGAGGCG GGCGACTGAG CAGAGTGGGT TCAGGAGGCA GAAGACCCTG GGTGTAGCCT 780
TGGATCCTCT GTCAGAGAGC AGCTTCAGGG TCTGGTCTCG GGAGCAACTG CCCTCCCTGC 840
TATGTGACCC CCAGCTGCTT GCTGGAGTCT CTGGGCCTGT GGGATGGGAG CAGACGCTCC 900
TCTACCGGCT TGCTGCCACA CGCGCGTCAC GGAGGGGGCC ACGGTTCCTG CGCTGGGCAC 960
TGTTGGCCAC GTTGTTGAGG GAGGCGACAG GGGCCTCTGG GGCCTCGGGG GCAGAGCCAG 1020
AGCCCAGGGG TGAAGGCCAA GTCCCAGGGG GCAGCCCTGG GCTGGGCCCC AGGCCTTAGG 1080
ATGCCCACCT GGTGCAGCTT CTCAGCCCAT CTGGGCAGCT AGGAGAGAGA GAATAGTGCT 1140
GGCTGCACCG GCAGACACAC CCCCTAACCT CACGGCACGA GCCCGAGGGA ACGTCATGCT 1200
GGCACCCCCT TCTCCATATG GGTAAACTGA GGCTCAGAGC ACACACAACC GCTGGCAAGC 1260
TGGGCAGAGG CAGGACTTGG CCCCAGGCCT GTGGATTCCA AACCCCAGCT CTCCCTCCCC 1320
AGGCACCCCC AAAAGGCCCT GGACCCTGGC CAGACCCACC GGGCTCCCCT CAGCCAGGTT 1380
CCCCACTCTG TGGGGTTGGC TCAGCCAGCA GCGCCAAGCT CTGCCTGGTC CTCGGTCCCC 1440
CACTGCTTCC ATCCCCATGG GGTGTAATCG GAGGGCTTTA AGACCCATGT GGACCTTTCA 1500
ATCATATAAA TATGCAATGG CTGGAACTTC TCATTTGGTT CCTCGCAGAT GCCTGGGGGT 1560
GAAATTGAAT CCCAGCACAG CGTGTTTGTT CTGGAAATGG CGTGTGCAGT CTTGTTTGCC 1620
TGAATAAATT AGTCCTTGTC CCAGTGCTGT GCCTGTAGTG GCGGCCCCAT TCCCCTGGCT 1680
GGGCTCACCC ATGCGGCCTA GGTCCCGCCC CCTCCTCAGG AGACCCGTCT AGAGATGGGG 1740
AAACTGAGGT CAGAGCAGGA AGAGTCAGCC ACGGGGCCAC CAGCCGCTGC CTCCCACCTC 1800
AGCTCAGAAG AGCCCTGGGG CTCTGGTTCA AACCCACCCA CCCACTGCCT ACCCTTGGGC 1860
CAGTTGCTTA ACCTCTCGGA TCTGTCTCCC CCATGTACGT TGGGAGGAGT AACTTGAGCA 1920
CAGCTGGAAA GAATCCTCAC AAGTCCTGCT GGGCCTGGCT GAGGCTCGGT CCGTGGGGCA 1980
GGTACTCAGT 1990
|
