| Tag | Content |
|---|
EnhancerAtlas ID | HS108-38701 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr8:8966360-8967590 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYB | MA0100.3 | chr8:8966604-8966614 | GACAGTTGGT | - | 6.02 | | SOX10 | MA0442.2 | chr8:8967044-8967055 | TCCTTTGTTTT | - | 6.32 | | Sox3 | MA0514.1 | chr8:8967045-8967055 | CCTTTGTTTT | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27764 | chr8:8965682-8967092 | Fetal_Intestine | | SE_28660 | chr8:8965442-8967304 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 8966447 | 8966966 | | chr8 | 8966486 | 8966781 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I009108 | chr8 | 8965552 | 8967023 |
|
Enhancer Sequence | GTGGTATCAT TTTTGCTTAG TTCTGCCCCT TCTATGGTAT TCTCTTTTTT AACATAATAC 60
CCTCTGTGTC CCACTATATA CTTTTTACAA AGCTGGCTCT GGCTCAAGCC AAGGCCTCCT 120
CTCTGGCACC ATGGAATTTC TGTAGTGAGA TAGGAAAAAT CTATTGTGCT CTCAGAGTCA 180
CAGACACTGA ACAGCACAGC AGGGGCCAGG TTATCAGTGG CCTCTTCTTC CAGAGTTCCT 240
GTAGGACAGT TGGTTATCTC AGCCTGTGCC CAGTCAGCCT ACACGTGGGG GTCTGGGTAG 300
TAAAAGCTGC AGAGAAAGCA GCTCTGTCCA GATTCATTTG ATTAACTAGA CAGGCACATC 360
AACTATACAC CCGTTCATTG CATTGCAGTA TCCTGAAACT CAGGGGCACT TGAAGGGGAA 420
GAGGAAGTAG CTCCTGCCTC TGGGGTGCTT GTAATCATAT GGTAGTGAGA CACCCATATC 480
CAAAAGAATG AGAAGAAAAA TCCCAAGATG TTAGAGATGC AAGTGCCTCA TAGGGAGGTA 540
GAAACTGTGT ACACAATGCT GAGAGAACAT CAAGTAAAGA GAAGCAACTC CATTGGTTGG 600
GACAGAGCAA CATCATCCCT TGTTTCCTTA AATTGCCAGT AAATATTTAT CCTCTGCTTG 660
CTTCTGCTTG GGGCCAAATC ATTCTCCTTT GTTTTAGAGA GAAGGAAGGA GCCCCTCTGT 720
TCTCCCCTTC CTGGGAAATT CATCGCACCA ACAGCGGAGA TCTTGGCTTT TTACACTATT 780
TTGGGGGCTC TGCTTGGCAT AAAATAATAC ATTCCCTGCC TGGGGCTAGG ACAGATTGCT 840
GCTTTTCTCC CACCTCCTGT AGGGTACATC TGGCCAACCA TCCCGATCAT TGTTTGCAAA 900
GCTTCTATTC AAACATGTAT ATTGTTTTAT GAATGGCAAA AGAGGAAGCC AACAATAACC 960
TTAGGTCTTC ATCTGCTTCT TTCATCTGAA GGGCGGGATG ATTCTGTGAA GTTCCCCTCC 1020
AGCCAGTGTC CCATGCTCTC TGTTTCCTGG GAAGCCAAGA TCATCAAGAT CATAGTCTTC 1080
TTTTGCTCAC AGCACACCCA CTCCTGGAGT CCCAAACCCC ATTCCTTTCT AAATCCTACT 1140
ATTCTTAAAT ACTCTCTTTC CCTGGTGACT TTGTATCTGA ATGGATTATT TGAAACTTCA 1200
ATGGTGCCTT ATAGTGTTAG GAATTGTTTT 1230
|
