| Tag | Content |
|---|
EnhancerAtlas ID | HS176-19761 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:19807370-19808520 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:19808427-19808448 | CTTCCTACTTCCCTCTCCTCC | - | 6.18 | | ZNF263 | MA0528.1 | chr2:19808411-19808432 | TTCTCCTCCTTCTCTTCTTCC | - | 6.31 | | ZNF263 | MA0528.1 | chr2:19808405-19808426 | CCCACTTTCTCCTCCTTCTCT | - | 6 | | ZNF263 | MA0528.1 | chr2:19808402-19808423 | CCTCCCACTTTCTCCTCCTTC | - | 7.36 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I019607 | chr2 | 19806936 | 19809433 |
|
Enhancer Sequence | ATTCTGGCTT TACCTCTTTC CCAGGATACT GTACTTTAAG AGATGTAGCT CTAGGCAGTA 60
ACATTTTGTC CAAAGGAATT AACTGCAATG GTGGAATGTC TGGTATAGTG AAAAAGATTC 120
TTGCATATAG GAGACCTTCT AAGCACCCCC AACCACACAG TAGAGGACAC CACTGAGCCT 180
CCCTGTGGCA AAGCCAGTCC TTCTCTTAAG TTATATCAAC ACAAGCACCC TTCAGCAGTT 240
AAGTTTCCTG GAACATCCAA AGATTCATTG ACTTATGCTT TGGAGGAAGA TTTACAAGTC 300
CTCTTTTGTA AAGAGAAGTT CGCTATGTGA CTTGAGTGAG ACAGAACATC ACTTGCTTTG 360
ATCCTTGCAG AAACAGGATG AGAGGTCCCA AGATTCTGAC TCACTATCCA TTGCCCTGAC 420
CCTGAGCAAC CCAGCCTCGT CCTGGTCTTA AAGTGTATTG GCACTTTGCT GTCTGTTCTC 480
CTTCCATTGC TTTTGATTTT GCATACCCTG AGTCATCTCT GAAGATTCCA TGCAACCAGC 540
TGGGTGGCTG GCATCCAGCT CTGTGACACT TGCCTTGATT GATGTGCATC CTCTTAAGCA 600
TCTGCTCACG ACAACTGTCT CTACCCTGAA GATGACCAGA AGGGACTCCT CATCTTGCTT 660
TACCTGTCTT CAGCACTTAG CCATTAGGCT GTTACCAGCA AAGCTGTCCT TTTCTCATAA 720
CAGATCGGCC TGATTGTGTA ACTGTATCCC TTTACTTCTG ACAGCATTTT CAGCTTTGTG 780
TAACCTCCAA ACATATGAAT AATTTTCACT TGTGCATTGC AATGAGCTTG GGGAACATTC 840
AGAGTTCAGA GGTACAGCTA GAAATATGTC CAGAAGGATG AGTCAAATAA TGTTGGGGGT 900
GACTGGGAAA GAGAAGAAAG GGTCCTGCCA TGCCTCTCCT GTGAGCCAAC AGTCTGATGC 960
GCACTTCAGG GTCACTGTTT CCAGTGTGCA AGTCCTTGGC TGTTGGAATG AAATGTCTGC 1020
CTCTTTGTTC TGCCTCCCAC TTTCTCCTCC TTCTCTTCTT CCTACTTCCC TCTCCTCCAA 1080
TTCACCCCAT GAAAATATTG CATAATGTTC ACAGATAACC CACTAAGCCT AGCTTAGTCT 1140
ATTAGGAGAT 1150
|
