| Tag | Content |
|---|
EnhancerAtlas ID | HS176-22155 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:173310520-173311720 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:173311512-173311533 | TTGGACTTTCATTTTTCCTTG | + | 6.07 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_18780 | chr2:173310953-173311877 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_27809 | chr2:173310336-173314519 | Fetal_Intestine | | SE_28663 | chr2:173310266-173314672 | Fetal_Intestine_Large | | SE_31796 | chr2:173310322-173310818 | Gastric | | SE_35837 | chr2:173310261-173315839 | HMEC | | SE_50315 | chr2:173310287-173311002 | Sigmoid_Colon | | SE_52439 | chr2:173310257-173311016 | Small_Intestine | | SE_52439 | chr2:173311184-173312029 | Small_Intestine | | SE_64259 | chr2:173310293-173311938 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I172445 | chr2 | 173310417 | 173315535 |
|
Enhancer Sequence | CACCACTGGA GCCTCAACCT CAAACTCAAG GTGGTGGCAC CTACATTCCA GGCAGCTGAA 60
GAAAGGAGCA AAGAACAGAG CCAAAGGCAC ATGCATGCCA TCTTCTAAGG AAAATTATTG 120
GAAGCAGCAG TGTGATGCTT TGTCACACGT CCTATTCAGC AGAACTGAGT TGTGTGGCAC 180
ATCCAGCTAA AGAGGGAGGT TCAGTTGAGT AGTAGTTATT CAGGGTGGCC TTATGCCCAG 240
CTAAAAAGTC TTTTACTATG GGAAAGAGGA GAACTGATGT TGGGTGACAG CCAGCACTCT 300
CTGGCAGAGC TACTAAGCCT GTTGTTTCAT TTATCTCATT TAGAAAATAA ACTGTGACCA 360
TATTAATTTC CTTTTCAAAG CATTGAAAAA TTTGTATTTC CTAAACTATT GGAGTAGTAA 420
AATGGGTATG GTGACCCACC AGGTGTGAGC TCATTAAGTC TATCTTTTCT CTTCTTGTTT 480
TTTATTTAAA ATATTTTATT GAAAAATGAT GGAATTTAAA GTCGCTTTTT CCTTTGCAGA 540
TGAACTATTT GATAACAGGT TTTAAGACAT GAATCTTATT TTTTGAGTTA ACACTGATAA 600
TATTTATGCT TGGTACACTT GAAATAGAAA AACCTGCTTG GTCACAACAT GCTAGAATTT 660
AAAATTATTA AAAGTGATGA ATTAATGATA AAACTTTATT CCCATAACAG AAATTTACTA 720
AGCATCTACT ATGTGCCGAG CACTGTGCAA AGGTCAGGGA TGGAAATGGT GAGCTCACAA 780
TCCAAGTGTG TACAGTTTCC TAGACTTGGT TTCTTGAAAG GAAAACTCAC TAGAGATTGG 840
ACTCCAAATC ACAAATGTCA TTTGGCAACT GATAAGTCGG GTATCTGGTA ATTCAGAAGC 900
ACAGGAAATG ATTAAATGCC ACATTTGACA AGATCTGGCA GCTGCCTTGT GAAACTGAAA 960
GAACAGGATT GCCTGGAGAC AATTATCAGA ACTTGGACTT TCATTTTTCC TTGCTGCAGT 1020
AGACAGTGTT TTATTGTGGC TCTTTAAGAG ATGTCTTAGT GGTATGAATT GCTTGGTCAG 1080
CTGAAAACTT TTCACCTAAT TTAATTTTAT TTTTAATTTT TTTGAGACAG AGTCTCACTC 1140
TGTTGCCCAG GCTGGAGTGC AGTGGCGCAA TCTTGGCTTA GTGCAACCTC CACCACCCAG 1200
|
