| Tag | Content |
|---|
EnhancerAtlas ID | HS176-10097 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr12:89783960-89785450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr12:89784009-89784026 | AGGTACAGCGTGTTCTG | + | 6.32 | | GATA2 | MA0036.3 | chr12:89784160-89784171 | GAAGATAAGAA | - | 6.02 | | 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 | GCTTTCAGCA GCCCGGTCCA CAGACCTGAA CAATGGTTAA TGTTTAAAAA GGTACAGCGT 60
GTTCTGCTTA ACAACTCTGC TCATTTCCTC TTCCTGATGG TGCTGCTGTG ATTGCAGAAC 120
TCAAGTAAGG GCTTTTTACT ATATGAGAAT ACATGAGAAA TGATGCTCAA GTCATAATAA 180
ATGTGAGATT AAGGTCACTT GAAGATAAGA AGGTTGCAGC CTTAAGGAAA AACTTCAGTT 240
GGCTTGGACC TCTGCGGGGG CAGGTTTACT GTAGTTTGTG GAAATAACCC ACAGCTACTA 300
CTGAAATATG TGTAAGGATT TCAGACAGGA AATGAAGGAA ATGCTGCATT AAACTAAAAG 360
CACTTTAGGA TTTAAATAAG CCGAATATAG ATTCTCTGGT GAGAATTTGA TCAGGGCACT 420
GCTGGCATTG GCCCACCCTC TCATCTACAG TAGTGGAATT ACAGTCTGCC TATCAAGTCC 480
AGAATACAAA GTGCTTTCAG TCCTCTGACT ATCCTCTTTC CTCTTTTATT AATTCCATTT 540
CTCATTAAAA TCCCCTGTAC AATGTTCCAT GAGAGTGAGC TCAAGGCAGC TACTGACATT 600
TCCCATAAAT GATACGCCCA ATCTTCTTCC TACTAATCCA ATTAGTTCTA CTTCCTTCAA 660
ACTTCATTCA AAACTCAACT CATCTGATCT ATGCCTGATG ACCTTACAGT CATTCCTTGT 720
CACTGTAAAC CCTCAGCAGT TATTGTTGAC TGATTTGCTC ACTATGACCA TGTGTTTACT 780
TGTGCCTGGC ATTAGGCTTG GTGCTGGGGC TACACTGATG AGTAAACCCC AGTCACTGCC 840
CTCATGGAGG TCACAGTTCA CATGAAAAAA ACATCCTAAT AAACTGTGAT AAGGGCAATG 900
GTCAAGATAG GCATGCGGAA GTATGAGGAC AAGACATTCA TCCTCTGGGG TGTCAGAAGG 960
CTTCCTGGAA AAGCTGATGC CTGAGCTGGA TTTTCAAGTA GAGGAAGGTC GGGGAGATAT 1020
AGATGGTAGG TAGTGTAATC CATGAACAGT TGAGATGGCC CTGTGTGCCA TGGTATGCTT 1080
GGGTGTATTC ATGACTTTCA CTTCATGAGA AGTTCCCTGT ATTTGGGTTC TTTTCCTACA 1140
ATTGAATTAT AAGCTCTTCC AGGAACCATA TTTTCTACTT ATTTTGCCTT CTTCCCCTTG 1200
GGTCTCTTAC AGTCCCCAGA GAGTTTTAAA GAGTTGTGTT TCACCATCCT GGGAAACACA 1260
CTGCTGACTC ACTGACCACC TCCAGGCCAC TCTGCCCACC GTGTGTTAAC AAGACTGTGT 1320
GGCCATGGAA AGATATGTAA GGCTGCAAGC CTTTTATCAG CTGTCAGGAT AGACCCAGGA 1380
AGACACACAG GTCTGACTCA AAGCACATAT ATACTGCCTA ATGGAAGAAA CCATCCAAAC 1440
CACTTACCCA GAAGTTCCAC AAGCCCATCA CATGCCATCC TTCCACTATT 1490
|
