| Tag | Content |
|---|
EnhancerAtlas ID | HS133-07846 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:89784250-89785440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PHOX2A | MA0713.1 | chr12:89784593-89784604 | TAATCCAATTA | + | 6.02 | | Phox2b | MA0681.1 | chr12:89784593-89784604 | TAATCCAATTA | + | 6.02 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_25078 | chr12:89784165-89785524 | Colon_Crypt_3 | | SE_27644 | chr12:89782519-89785793 | Fetal_Intestine | | SE_28566 | chr12:89782048-89785987 | Fetal_Intestine_Large | | SE_35767 | chr12:89782928-89786699 | HepG2 | | SE_38298 | chr12:89782753-89785888 | HUVEC | | SE_41177 | chr12:89783038-89785367 | Left_Ventricle | | SE_48925 | chr12:89783907-89785560 | Right_Atrium | | SE_50215 | chr12:89783892-89785574 | Sigmoid_Colon |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I089388 | chr12 | 89782568 | 89786661 |
|
Enhancer Sequence | ACAGCTACTA CTGAAATATG TGTAAGGATT TCAGACAGGA AATGAAGGAA ATGCTGCATT 60
AAACTAAAAG CACTTTAGGA TTTAAATAAG CCGAATATAG ATTCTCTGGT GAGAATTTGA 120
TCAGGGCACT GCTGGCATTG GCCCACCCTC TCATCTACAG TAGTGGAATT ACAGTCTGCC 180
TATCAAGTCC AGAATACAAA GTGCTTTCAG TCCTCTGACT ATCCTCTTTC CTCTTTTATT 240
AATTCCATTT CTCATTAAAA TCCCCTGTAC AATGTTCCAT GAGAGTGAGC TCAAGGCAGC 300
TACTGACATT TCCCATAAAT GATACGCCCA ATCTTCTTCC TACTAATCCA ATTAGTTCTA 360
CTTCCTTCAA ACTTCATTCA AAACTCAACT CATCTGATCT ATGCCTGATG ACCTTACAGT 420
CATTCCTTGT CACTGTAAAC CCTCAGCAGT TATTGTTGAC TGATTTGCTC ACTATGACCA 480
TGTGTTTACT TGTGCCTGGC ATTAGGCTTG GTGCTGGGGC TACACTGATG AGTAAACCCC 540
AGTCACTGCC CTCATGGAGG TCACAGTTCA CATGAAAAAA ACATCCTAAT AAACTGTGAT 600
AAGGGCAATG GTCAAGATAG GCATGCGGAA GTATGAGGAC AAGACATTCA TCCTCTGGGG 660
TGTCAGAAGG CTTCCTGGAA AAGCTGATGC CTGAGCTGGA TTTTCAAGTA GAGGAAGGTC 720
GGGGAGATAT AGATGGTAGG TAGTGTAATC CATGAACAGT TGAGATGGCC CTGTGTGCCA 780
TGGTATGCTT GGGTGTATTC ATGACTTTCA CTTCATGAGA AGTTCCCTGT ATTTGGGTTC 840
TTTTCCTACA ATTGAATTAT AAGCTCTTCC AGGAACCATA TTTTCTACTT ATTTTGCCTT 900
CTTCCCCTTG GGTCTCTTAC AGTCCCCAGA GAGTTTTAAA GAGTTGTGTT TCACCATCCT 960
GGGAAACACA CTGCTGACTC ACTGACCACC TCCAGGCCAC TCTGCCCACC GTGTGTTAAC 1020
AAGACTGTGT GGCCATGGAA AGATATGTAA GGCTGCAAGC CTTTTATCAG CTGTCAGGAT 1080
AGACCCAGGA AGACACACAG GTCTGACTCA AAGCACATAT ATACTGCCTA ATGGAAGAAA 1140
CCATCCAAAC CACTTACCCA GAAGTTCCAC AAGCCCATCA CATGCCATCC 1190
|
