| Tag | Content |
|---|
EnhancerAtlas ID | HS106-01234 |
Organism | Homo sapiens |
Tissue/cell | iPSC |
Coordinate | chr2:85186270-85187560 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr2:85186957-85186968 | ATGTAAACAAA | + | 6.14 | | JUN(var.2) | MA0489.1 | chr2:85186484-85186498 | ATGACTCATTACCT | - | 6.18 | | NKX2-5 | MA0063.2 | chr2:85187414-85187424 | CTCAAGTGGT | - | 6.02 | | ZNF263 | MA0528.1 | chr2:85187208-85187229 | CCCTCCTCCCTCCACTCCCCT | - | 6.38 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_27502 | chr2:85184750-85187659 | Esophagus | | SE_32926 | chr2:85184713-85187023 | H1 | | SE_32926 | chr2:85187157-85187722 | H1 | | SE_34685 | chr2:85184438-85187655 | HeLa | | SE_35873 | chr2:85183583-85187716 | HMEC | | SE_47378 | chr2:85183405-85188185 | Panc1 | | SE_52528 | chr2:85184768-85187231 | Small_Intestine | | SE_64856 | chr2:85184623-85187455 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I084956 | chr2 | 85183648 | 85188352 |
|
Enhancer Sequence | CCACGCTGGC TAATTTTTGT ATTTTCAGTA GAGACGGTGA AGCCATGTTG GCTAGGCTGG 60
TCTCGAACTC CTGACCTCAG GTGATCCACC CACCTCAGCC TCCCAAAGAG CTAGGATTAC 120
AGGCGTGAGC CACCGTGCCC AGCTGAGACG CTATAATTTC TAACCTATGG CTTCCCCTTT 180
TCTGGATTCC ATGCAGTCCA CACACAAGCA TTCTATGACT CATTACCTCC TGAGCATCCA 240
GCTTCTTAAC TGTTACATTC TAGGGATCTT TTCCACAGTA TGTTTCTAAC TCCTTGATGG 300
TTTTTGGGGG AGACCTGGGT GACACACTTG GAACAGACCT GCTCCAGGGG CTTGTTACTT 360
TGTGTGCATC CCGCTCCCTT CACTTTCAGG TGACCTCATT TTCTAATCTT CCTTAGAGCA 420
ACCAATCCCC CATACACTGT CTCCTTCTTC AGAGAATCTT TCTATGTGGA TTTGTGCTTT 480
TTAAATTGGC ATATGAGTTT TAGGCACAGT TGGACCAGGA AATGCCTTCC TGAGGAATTC 540
AGCAGCTTCT AGAGATAAAA TGTGATAGAG CAAATTATGA GTCTGGGAAT CAGGACATCT 600
GGGTTCCAGT TTTGTACACA TCATTCATTT CACAAATAAG CACCCAAAGC CCACTATGAT 660
AGCCAACTGC AGGGCTGTGC TACAAGTATG TAAACAAAGA CACCTACTCC TGCCCAAGGG 720
CAGCCCAGTG GGGGAAGTGA AAGGATTAAA TTGCAATAAT AGAGAATTGT AAAAGGAATT 780
GGGAGCACTT AGTGAGGTGG TTCTACAACT TTATTGCACC ATCAGGATCC CCACGGGTGT 840
TCTTTCAAAT GCCAATCTTT GAGCCCCATC CTTCAGAGAT CCTGATCCGG TTGATCTAGG 900
AATGCTCAGG GACATTGAAT GTTTATTCTG AGCACCTTCC CTCCTCCCTC CACTCCCCTC 960
CTGGTGATTC CACTGGAAGT GGCCCCAACC CACACTCTTT CCTTCAAGAA AAGGTTCACA 1020
AAGGCAGGGG TCTGGAGCTG ATTTTTTTTT TTTTTTTTTT TCCCAAGAGA CAAGGTGTTG 1080
CTCTGTCACC CAGGCTGGAG AGCAGTGGTG CAATCATAGC TCACTGCAGC CTCAACCTCC 1140
CGGACTCAAG TGGTCCTCCC ATCTCAGCTT CCCAAGTAGG AACTACAGGC ATGTGCCACC 1200
ACGTCCAGCC CTTACAGCAC ATCCAGCTCT TACAGCTGAT TTTTAAAGGA GGAAGGAGTA 1260
CAAACTTATG AGGCACAGAG GCAAAAAATG 1290
|
