| Tag | Content |
|---|
EnhancerAtlas ID | HS020-01398 |
Organism | Homo sapiens |
Tissue/cell | CD34+ |
Coordinate | chr1:44012290-44014420 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:44012855-44012875 | ACCCCACTCACCCACCACGC | + | 6.69 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_00616 | chr1:44009256-44025211 | Adipose_Nuclei | | SE_03403 | chr1:44011667-44013233 | Brain_Angular_Gyrus | | SE_03403 | chr1:44013288-44013976 | Brain_Angular_Gyrus | | SE_03403 | chr1:44013988-44014536 | Brain_Angular_Gyrus | | SE_04240 | chr1:44003988-44015177 | Brain_Anterior_Caudate | | SE_05040 | chr1:44001099-44015486 | Brain_Cingulate_Gyrus | | SE_05962 | chr1:44000439-44020958 | Brain_Hippocampus_Middle | | SE_07193 | chr1:44003475-44015024 | Brain_Hippocampus_Middle_150 | | SE_08033 | chr1:44003431-44015175 | Brain_Inferior_Temporal_Lobe | | SE_23218 | chr1:44005985-44017477 | Colon_Crypt_1 | | SE_23829 | chr1:44011550-44012644 | Colon_Crypt_2 | | SE_23829 | chr1:44012940-44013354 | Colon_Crypt_2 | | SE_23829 | chr1:44013362-44015343 | Colon_Crypt_2 | | SE_24870 | chr1:44006024-44012830 | Colon_Crypt_3 | | SE_24870 | chr1:44012836-44017627 | Colon_Crypt_3 | | SE_26649 | chr1:44010798-44020559 | Esophagus | | SE_27645 | chr1:43995619-44017587 | Fetal_Intestine | | SE_28595 | chr1:44005404-44017604 | Fetal_Intestine_Large | | SE_31538 | chr1:44004919-44019003 | Gastric | | SE_41575 | chr1:44001646-44015303 | LNCaP | | SE_47657 | chr1:44011019-44012837 | Pancreas | | SE_47657 | chr1:44013015-44015395 | Pancreas | | SE_50363 | chr1:44005822-44020588 | Sigmoid_Colon | | SE_52524 | chr1:44004832-44019377 | Small_Intestine | | SE_65452 | chr1:44004903-44018198 | Pancreatic_islets | | SE_69138 | chr1:44010309-44012639 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 44012854 | 44012939 | | chr1 | 44013344 | 44013400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I043539 | chr1 | 44005459 | 44020850 |
|
Enhancer Sequence | GCAGGGGAAG GATGGCCCAG TTGGGCTTCA ACAGATAACA CATCCTGGGA GAAGAGCTGC 60
CCTCCTCCTC CTGCCTCAGA CCCAACGCGC CCCAACCTGT ACCCCTCACT CTCATCCCCC 120
AGCCTGCTGT CTTCCCGTGT TCTCTCCCGT GAAAGGCATT ACCACCCACC CGGTCACCCA 180
AGTCAGAACC TGGGCCTCCT CCAGCCTCCT CCCTCCGTGA TATCCCACAT CTAATCCATC 240
ACCAAGCTCC GTTGCTTCTA CCTTCTGAAT ATCTTTGGAA TGCATCCACT TCTCTCTCTA 300
CCGCCTTCAT CCAAGCCACC CTCGGCTCTT GGGCTTTTGC ACGCAACAGC CTCCTGACGG 360
TTTCCCTGCC TCCAGTCTTT TCCTTCCTAA TCCATTCTGC ATTCCAAAGG TAGAGTCGTG 420
TCACAAGGTG AAAACATCAT CCTGTCACTC TTCAGTTTAG AATCCTTCAT TCCCTCCCAC 480
CCCCAGGCCC CCAGGGTCGT AACCCTTCTA TAGGCCCTGC ATTATCAAGC TTCTATCAAC 540
CTCATCCCTC GCTGTCCCTC CACCCACCCC ACTCACCCAC CACGCTGACT TCTTTCAGTG 600
GTTCACCAAT TCCCAGTAGT AATTGGTAGG GGCAAGGGGG AACAGTTTTT AAAGCAGAGA 660
ACCTCCATGC TGGTTCCTTA GGAACCAAAG CCCAAACACC AGGTCTTGAC GGTAGAAAGC 720
AGCTGAAGAA GCTGAAATCC TGCCTTCTTC AGGTAGGGGG TTCAGGGGAC TCAGGCCTTC 780
TCCCAGGCAG AGAGCCATGG GGCAGGAGCC TGGGCTGGGG GTCAGAGTGA CCGAGCCGCA 840
GGAGCCAGGG TCTGTCTTCC AGGCCTGTCT TACACTGCAC ACAGTTTTGG ATCTCTCCCT 900
GCACTGAGGC AGGGCTCAGG CTGAGCTTGG GCAACTACTA GCCAGGGGCA AGTGGCCATA 960
CACAGACAGG GCCACTGCAG AAGATAGGGT AGGCACCCCA GAGAATTGAC AGCTGGGGCA 1020
GTGAAGCGCG GAGTGGACAA ATGTGTTTCA ATAGGCCTCT TAACGAGACA AATGAATGGG 1080
GGCCCTGGCC TCTGAGGGGA GTGGAGGGAA GCGGGTGGAG AAGCAGCTGC CAAGAGTTAG 1140
CCCAGAGGCC CCAGTGTCAG TGCCGCACGC GCAGCTCCAG TGGAGATTTG GGCACACATT 1200
GGGGTAGGAT CTGCTGCAGC GCAGCTTCCC CAGCCAGGCT TTGTGGCTTC TCAGGAGGGG 1260
AGGTTGTGGG GCCAGAGGTG TCCTGAGCCA GGGCAGAGGT TTTTGCTGAT CTCAAGTGCG 1320
TGTCGCGTGC CTGTCTTCAG GCAAGACCTG CAGTGTGGAG GCACAGGCTT GTGAGCAGTG 1380
ACCACAGGGT GTGCTGGGTA GGTGGCACTG ACACAGGCCA TGGCAGAAGC ATCTTGGGAG 1440
AGGAGTTGGG AGGCTTCCTG GAAGAGGGGA GCCCTGAAGG GTGAGTGGAC ATTTGCTAAT 1500
GGGGGGGTAT TGCATAATGA GGTGGGGTTG CGGGGAAGAA GCACGAATGT GGCTGGGCTT 1560
CTCTGTGGAA TTCATGGGAG AGCCACAGTG AGAACCCGAC AGCATGGGAC AGAGGTGGGG 1620
TCCGAAGACC AGGTGGGAGT GAGACCCTGG TTATGGCCCA TTTACCCAGA ATCCTAGGAG 1680
CTCAGAGCAG GATGCGTGCT GGCTGGAGGG GTGGGTGGCG GGTGGGTTGA CAGAGGTGGG 1740
CAGAGGCTGA GGAGCTGGGA GTGTGTCTGT TGTGTCATTT CCCTCCTCCC CAGAGCCTGT 1800
GGAGCACACA GGGTCTGTTG TCTGTCGTCA TGCTCTCCCC CTCGTTCTAT GGGTGGCCTG 1860
TCTAGACTCT GCTCCCTGTG GGACTTCCCG CAGATTCCGT TGCTTTCTCT CTCTGGGCCT 1920
GTTTTCCTAT TGCACAATGG GGATAATCAC TCCTACCTGG AAAGGTTAAC TGAGGTCACA 1980
TGGATGAGGT GCCTGGAACC TAGTATGTAT TCCCCTTATC TGAGGCCATG ACCTGGGGCT 2040
CTTGCTCTGT CCCTGGGAAC CAGGCTTGTC TCTGAGTGGG CTCCAGGGGG GTACCAGGAA 2100
CAGTCACAGG AGCTCACTGA GTCCCAGCTT 2130
|
