| Tag | Content |
|---|
EnhancerAtlas ID | HS007-15145 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr7:2774310-2775680 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr7:2774786-2774807 | TCTCCTGCCTCCTCCTGCTCT | - | 6.27 | | ZNF263 | MA0528.1 | chr7:2774780-2774801 | CCTCTCTCTCCTGCCTCCTCC | - | 7.29 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_08508 | chr7:2774377-2775864 | Brain_Inferior_Temporal_Lobe | | SE_13053 | chr7:2772498-2776851 | CD34_Primary_RO01480 | | SE_13522 | chr7:2770820-2777015 | CD34_Primary_RO01536 | | SE_14094 | chr7:2767596-2779169 | CD34_Primary_RO01549 | | SE_65933 | chr7:2772654-2777111 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I002727 | chr7 | 2767350 | 2775713 |
|
Enhancer Sequence | CTTCCTACTT TAGAACGAAG GCCTCTGGAT GTTTTCAAAG TGAGTGTTTT GTTTGAGGGG 60
ACAGAAACAC ACGTCTCCCC ATCCCAGCAC TGCCTGTGTT GAGCGAGCAC ACATCCTCCT 120
CCTCTGTGGC AGGACGGGGC GAGCACGTGC ACCTCGTGAC CACCGGCTCT CTAGAGCCCC 180
AGGCAGAGGC CCAGCTCTGC AGTAGGGAAG GCATCGGGAG TGCCAGGGTG AACGTACCCC 240
AAGGGCCCGG CACGACTGAC CTCTCGTGCC TGCTCTCTCC CTTCCTCGCC AAGCCCCCGT 300
GATGTGGGAA GCCAGCGTGA GGCCGGTGGG GCAGCCGCCT TCCCGTGGCT GTGCCAAGTC 360
CCCCCGGTCC TCTGCACATC ATGCCTCCTT CCACACCCTG ACAGGAAGCA GCTGGGAGAA 420
GCCGTTGGGT GCACTCACTC CCTGATTTAC GACAAGTTCC TTCCTCAGCG CCTCTCTCTC 480
CTGCCTCCTC CTGCTCTCCT GCCCTCCCCT GGGCCTCGGG AGGTGCCACG CAAGCCCAAG 540
AAGCATCAGC ATACTGTCCC TCCCTCTCCT GTGGCCACGG GCTCCCCCAG GGAGCTGAGA 600
GTAGCAGCAG CTCACAGCCC AAGCCACCCT TGCCCGTTTC TAGGCAGGTG GTGGCACCAG 660
GCACGAAGGA AGCAGAGGCA GTTCTCCTGC AGGGTTCTAG CTGGGTCAGG CATGGAGAGT 720
CACAGTGGCA CAGATGCCCC AGCCAGTGCT CTTATCACCA CAGGACACAA AGCCCTGGAC 780
ACACGTGCTC CGCCCAGATA GTACGGACGC AAGGGGAAAA GCACCACAGA GGGCACAATC 840
AGGACAAGCT CGATGGGAAG CAGAAAACAG GAGGGACGTT TCCCTCGGTG TGAGTCTAAA 900
CACCCCTCGA GTCTGCAATC AGTCCCCCAG CTGCACTTCA CAACACAGCA AACACTCACT 960
GCTGCTTTCT CCACGATGAC TGAATGAGGA TGGCTCATTT AACTCATCAC AGCATTTGTA 1020
TCACTACTTG GAATGCAGGA AAACTTATCT GTGACTCTCG GTCATCTTGC ATGAGTGGCG 1080
GAGGAGAGGA GTCAAATCTA GTTTCATGTC AGGGCGGCCT CATCTCGAGA AACAGCCCAG 1140
GGGGTCCGTG GGAAAGCTGC CACTGAACTG TAAGGTGCCA GGGACTGTGC CACAAGCTCT 1200
CTAATGGGGG CTGGAGGGGA GGGAAGAAGG GGACACAGAG CAACCCTGTG TGATCCAGAA 1260
CGCTGTCACT CACATCCGCA CTCTTGCTGT CCCTGAGGTT TGGTGCACTG CGGTTCACCA 1320
ACAGAGACTG GACAATGCAC CTGCTGATTG GGCACGCAGC CCACGGGACG 1370
|
