| Tag | Content |
|---|
EnhancerAtlas ID | HS180-45968 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr7:134040440-134041820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SNAI2 | MA0745.2 | chr7:134040579-134040589 | TGCACCTGTT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr7 | 134040807 | 134041104 | | chr7 | 134040544 | 134041117 | | chr7 | 134041399 | 134041740 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I134355 | chr7 | 134040341 | 134041522 |
|
Enhancer Sequence | GTTTATATCC AAACTCTAAC ATCACAAGAA ACATTCTCAG GGTGCCCACC CCATGGGGGG 60
ATTGTATAAT CAACTCACAT TCATTAATGT AGTATGTGCT GACTTAAAAC CCAACGGGAA 120
TTTAATGTAA CTTATATTAT GCACCTGTTG TGTATTGGGT AAGGTACAGT GTTCAGTTCC 180
CTGGAATGTA GAATGCATGT AATTACCCTC TTCCAAGTTA ACAAACAACC CCAGGTAAAG 240
TTAAATAATC AACAGAGTGA ACCAAGGATT ATGCATTAAA ATAATTTTGG TGTTTTGCTG 300
ATCATATGCC CAGTGGGGTT TGGAAGGTTG CACAATGGCA TATTGCTAAA CATTCCAATG 360
CCACATTACC ACAAAAACAC AAAACACAAA AACGTCACAA GGTCCAGAAA GACTCCTCGT 420
GTGGACTTTG CTTCTTTATT TGCCAGGAAG CAGTTTGGCC CGAGCAGTTC TTTTTTGACT 480
GTAGGAAGTT GAGGGCAAAG TAAATCTGGC AGACAATGAG CCCTGGGCCA AGCTGCACTC 540
TTAGGATAAG ACAGGCTGTG AAGAGGGCCC TGTGGCCAAC TTCCCGATGA AGCTGTTGGC 600
ACAGAAGAGA AGGGGAGCAG GAATCCTGGC TGGCAGCTTT TACGGGAGTG ACTGAGCAGC 660
TTTTTTTTTT TTTTTTTAGA TGGAGTCTTA CTATGTCCCC CAGGCTGGAG TGCAGTGGCA 720
CAATCTCACC TCACTGCAAC CTCCGCCTCC CGGGTTCAAG TGATTCTCCT GCCTCAGCCT 780
CCCAGGTAGC TGGTATTACA GGTGTGCACC ACCACGCTGT GCTAATTTTT GTATGTTTTA 840
TAGAGATGGG GTTTCGCCAT GTTGGCCAGA CTGGTCTAGA GCTCCTGGCC TCAAGTGATC 900
CACCCGCCTC AGTCTCCCAA AGTGCTGGGA TTACAGGTGT GAGTCACCAC GCCCAGCCCT 960
GGGCAGCTAG CTATCTTGAT AACATCTGCC ATCTAAGAGG ACATTCATTT TGCCAATTTT 1020
ATTGTCACCA ACAACGTAAT ATTTACCCTT GGAAGTGATA AGACTAGGTG GATCTACTCT 1080
CTTCCTACAT TAAACGGGAA GTTGATATAA TCACTGAAGC TGCTATAAGC TTCTTTGAAT 1140
AGCAGAGCGT AGACCTGGTG AGACAGACCA ATGCCTTCAG ATCTGAGCTT AACAGAGCCT 1200
GCCTATGATG ACTAGTGACA GGTGCTTGCA CACTATTTTC CACAGGCCCA TCTGGACTGC 1260
ACACACTCAA CGGATGCCAA TTACATAACG ATCATACACA GCTGGGAATA GACCCACTTG 1320
TACAAAATGG ATCCAGTGGT AATGGTGTCT CCCCATTCTC ACCTTCATAG CGATGCTTTC 1380
|
