| Tag | Content |
|---|
EnhancerAtlas ID | HS176-28567 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr4:13921870-13923210 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr4:13922783-13922797 | CTGACTCATCTTCT | - | 6.12 | | NFE2L1 | MA0089.2 | chr4:13922765-13922780 | CTTGCTGAGTCATTT | - | 6.88 | | Nfe2l2 | MA0150.2 | chr4:13922767-13922782 | TGCTGAGTCATTTAG | - | 6.71 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_02362 | chr4:13918710-13924781 | Astrocytes | | SE_36504 | chr4:13918760-13924205 | HMEC | | SE_44315 | chr4:13917989-13926601 | NHDF-Ad | | SE_44831 | chr4:13918729-13925052 | NHLF | | SE_45641 | chr4:13917765-13926711 | Osteoblasts | | SE_55743 | chr4:13916905-13925023 | u87 | | SE_64944 | chr4:13919912-13923788 | NHEK | | SE_67669 | chr4:13916905-13925023 | u87 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I013916 | chr4 | 13918139 | 13926289 |
|
Enhancer Sequence | TCTGTACTTC TTGACTCTTT GAGTACACTT TGGAGCTGCA GAGATTGGGG AGCTGAGTGG 60
ATGTCAGAGT GTATGTTGTA GAAGAGAAGC TGATGTTTTT CAAAGCATTG CATCAGCATA 120
AAGCAGGGCC TTGCACGCAT ACATGTGTGC ACACACACAC TCAAAAAGTA TTACCGGCAG 180
AAAAGATTAT GAGACAACAC TTTTATTTTA CAAGTGAGAA AACAGAAGCA GAGAGAGCTG 240
ATGGCACAGG CACAGGCTTT GCCATGCTGG GGATGAGATC CAATTCTTCT GATTTCTTCT 300
TTGAGGGCTC TTTAACTCAC CCCGCTGTGA CTCAGCTTTC ACAGGGTGCT CTTCTGGCTT 360
ACAATCCCAA GGTTCGAGGG AAATTCCACC CGATTTCACC AAATACATTT TCACCTGACG 420
TTGCATAACG AAGTCACCTG AGCTTGCAGT GATTCACTCT GCAAGTACCT TGATTCACCC 480
AGCCCACACC TCAAATTTTT GATGCCCCAT TTCTTCCCAT AAGCAGGCAT TGTGCCTTCA 540
GTAGGTGGTG GAGAACTTGT CATGAGAATG CTATAATCCT TTCCACATGT TTGAAATTGG 600
TACTTTTCTA AGTTCCTTAG CAACCATTGT CTCATACAAT CTTTCCAAGA GTCCCGTCAA 660
TAGGCAGGAA AGTTGCCATT ATCAACCCAT TTGGGAGATG AACTTAACTT GGGCTCAGAA 720
ACGACCTGCC TCAGGCTCCT CCTGGGAAGT TTATGTTATT GTTATGGTAA CAGGATGATG 780
GTCACTACTA AGGAACTCCA GCCACATCCT CACTCGCCCT CACACAATGT CTTCACAGTC 840
CCATCTGCAT TTGCTCCAGC TGTGTTTCCA CCAACAACCT CAGTGCTGGT TCCTCCTTGC 900
TGAGTCATTT AGGCTGACTC ATCTTCTGGA CTCCAGAGAT TCCCTAACTG CATGCTTCAG 960
TTAGGGAAAG GTATGTTTGT GTGTGTGTGT GTGTGTGTGT GCATGCATGT GCATGTGTGA 1020
GGTGGTCCTT ATTAAATTCT TATCAGAACA CTTCAGAATA TTTGAACTGG CCACGACCTG 1080
ATTGCTTACT GATATCTGAG TGTCCCTTTT CCAAGATAGA AATGTAGTTC CTTGCTCTTT 1140
TCCAAATCTG ATTTGCAATA GCTGCTGCTC CTATAGATCC AGTCATTTTC CCCTTTTTTC 1200
TCTCTTTTCA TTTATTGATT CCTTCTTCTT CTAACCACCA CCAACAGTTT AGCCAAGATA 1260
ATGTAAACAT TTCTCTAGAG TCTGGCCCAG TCAATTCTCT TAGAGGCTCA TATTGTCCTT 1320
AAAATCTAAA TGATGCAATG 1340
|
