| Tag | Content |
|---|
EnhancerAtlas ID | HS050-59371 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr6:107860630-107862100 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RELA | MA0107.1 | chr6:107861656-107861666 | GGAAATTCCC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 107861534 | 107861839 | | chr6 | 107861600 | 107862092 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH06I107539 | chr6 | 107860261 | 107862438 |
| Enhancer Sequence | TTGACATATA TGCTGGAATG TTAATTTTCA GACATAGTAC ATCTCTGGCC ATCCTTCTGG 60
TGAAGGCTAA TGCTGTTCAC TTAAATCAAG TTTTTTCTCA TCGGAACTGC CGGTAATTAT 120
CCAATCCATC TAAAAGGCAC GCTCCCTTTT AACATTAACC ACAGTGTCAG ATTGCATCAG 180
CCACATTGTG TTCTGGTGAC TGCTTCTGCA GAGTGATGAA TGTGCGTGTT TGGAGTTCAT 240
AGTCCGACTG TCTGTTTGGG CAGTGGGCAG TTCAGTGAAA CAAATGATCA GGAAGGGATC 300
TATTTATTTG GGACGAACAT TCTCCTTATT GATCCAGTCA CTTACATTTC CAACTCTCTC 360
ACCTTGCCAC TAACAGTGTT CAGCTTTATC TGAAGAATGA GCGTTTAAAG AATTATCTTA 420
CAGGTCATTT TGATGTGATT CTCTGATCAT AAGCTGCATT CAGCACAAAG TTACTCTTTG 480
TGCCTGACTT AAAAAGGAAG GTGTTGTGAG ACTTTATTAA TAAAAAACAG AGGAGGGAGA 540
AGGTTCTGAG AGTGCTTGGT GAACTGTCCT GAGAAACCAA GAGATAATGA TTATTCTTTT 600
TCCTGGAATA GTAGTTATAC TCTGTTGATT CAGTGCTTTG TTAAAAATGT TAAGTATCTG 660
AATAAGTGCA GGCATAAAAG GGCAGGTGGC TTGCCTTGAG ATATTTTAAG GTAGTAGATT 720
AAGTCCTGAA TTTTTCTTGT ACACCTTTGC AATGTCTGGT CACAATGCCT AGTATAGTCG 780
AGAGGCCCCA TGGGGGATCC AAGCTATAGG CATGCCTGTG ATTATCTTAA TTTCTCCTCC 840
ATTTCAATAC CTCTGGATAG CTTATGTACA CATAAACAGA AGTGTGAACT GGCCAAGCCA 900
TATGTAATTC TTTGTTCCTC GGGCTCTTTG CTCTTTGTTT ATATTATCAC AGATTAGAAT 960
GGAATAAAGA AAATCTTGCT ACAGATGGTC ACTTCATTTC TGTCCCAGCA GTTGAGACTG 1020
AGAATGGGAA ATTCCCTATG TTACAATCCA CTCTTAGGGT GGCTGTGCAC ACAGTGGAAT 1080
CTAATGTCTA CTGACAGACT GCCTTTGGAG GTTACAAACA TCAGTCTATT GCATTCTCTG 1140
TAAACACAGG CTGTGGGCCA GAGCTGGGCT CTGCTACAAG CTCTGTGAGG CAGATCAATG 1200
GTTTAATGAA TCCATAAAGA TGCTTGAACT CTGCTGCAAT TTACTGAGCA CTCTAGTTAA 1260
ATGAAACTCC TGTAGTCTTT AACAAAGATA GTGATAATCG ATGGCTGGGG ATGGAAGTCC 1320
ATGTCCAGCA GTCACAACCT CCCAGAAGTT GTGTTGTCTC ATTGCTAACA GAGGTTTAGT 1380
CACATTCAGT TTCTGAGGCT CACTGTGTCT ATGTTGATAT TTGCTCAATG TTTGAGAGCT 1440
GAATTTGGCC CAGAAATGAC ATAATCTTAG 1470
|
| |
|
|
|
