| Tag | Content |
|---|
EnhancerAtlas ID | HS020-29659 |
Organism | Homo sapiens |
Tissue/cell | CD34+ |
Coordinate | chr22:40327880-40330650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr22:40328036-40328049 | TTCTAGAACCTTC | + | 7.12 | | NFAT5 | MA0606.1 | chr22:40330423-40330433 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr22:40330423-40330433 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr22:40330423-40330433 | ATTTTCCATT | + | 6.02 | | ZNF263 | MA0528.1 | chr22:40329930-40329951 | GGTGGAGGAGGAACAGGAACA | + | 6.08 |
|
| | Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
| SE_11932 | chr22:40328731-40330813 | CD3 | | SE_14493 | chr22:40329238-40335150 | CD4_Memory_Primary_7pool | | SE_17025 | chr22:40328670-40329353 | CD4p_CD225int_CD127p_Tmem | | SE_17025 | chr22:40329809-40330630 | CD4p_CD225int_CD127p_Tmem | | SE_17349 | chr22:40319007-40352007 | CD4p_CD25-_CD45RAp_Naive | | SE_17878 | chr22:40320347-40341946 | CD4p_CD25-_CD45ROp_Memory | | SE_18267 | chr22:40294463-40350394 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19208 | chr22:40326115-40335366 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_21542 | chr22:40329074-40335107 | CD8_Naive_7pool | | SE_21940 | chr22:40326204-40335616 | CD8_Naive_8pool | | SE_22388 | chr22:40294641-40335467 | CD8_primiary | | SE_25607 | chr22:40320595-40328473 | DND41 | | SE_25607 | chr22:40328779-40329719 | DND41 | | SE_30899 | chr22:40320591-40341995 | Fetal_Thymus | | SE_39453 | chr22:40326848-40328360 | Jurkat | | SE_39453 | chr22:40328632-40329541 | Jurkat | | SE_39453 | chr22:40329844-40330497 | Jurkat | | SE_55098 | chr22:40327941-40328362 | Thymus | | SE_55098 | chr22:40328811-40330962 | Thymus | | SE_62546 | chr22:40293885-40358119 | Tonsil | | SE_66359 | chr22:40326848-40328360 | Jurkat | | SE_66359 | chr22:40328632-40329541 | Jurkat | | SE_66359 | chr22:40329844-40330497 | Jurkat |
|
| | 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 |
| GH22I039930 | chr22 | 40326205 | 40341867 |
|
Enhancer Sequence | ATGCCTTTTG ACCCACACAA TATTAAAAGC AGCAAATAAC ACAAGAAAGG TAGAGAAAAC 60
AGAAGGTACA ACATTTTGTG GCTCACAGGA TATATGAGTG AGATTATATA CTTCTATTCC 120
AAACCACAAC CTTCACTAGA ACATCTAAAG GCTTCATTCT AGAACCTTCA TACTGCTTAT 180
CCCAAAGGCT AGCCCACTCC CCGGTTTTCA TGTAAGAAAT CTTGTGGGAC AGGCGTTGCA 240
TGAGGTGAGG GGCAGCAGGG AAATTCGAGA TGAAAGGGTG AAAAGATCAA ACGAGTCCTT 300
GCTATTCTTC TTAACAATGC TTCAGTCCAC CACTTTGAGA TTTCTGTGGA GAAAGTAAAG 360
ATTTGGGATA TACATATACT AAAACAACTA TTGGTTGCTT ATCTGAAAAT TAACTTTAGC 420
TGGGCATTCT GTATTTTATC TGACAACCCT ACTTGGTGAG GTGTACATTT TCTTATTCAT 480
ACTTCCTGCG AGCCACAACA TGTCTTAATA GTTGTTAGCT ATTAAGGACT ATGCATAAAA 540
GTGACAATAG CTGGCTGGGC ACAGTGGCTC ATGCCTTTAA TCCCAGCACT TTGGGAGGCT 600
GAGGCAGGAG GATCACTTGA GGCCAGGAGT TCAAGATCAG CCTGAGCAAC ATAGGGAGAC 660
CCCTGTCTCT ACAAAAAAAA AAAAAAAAAA AAAAAGCTGG ATGTGGTGGC ATGCACCTGT 720
AGTCCCAGCT ATTTGGGAGG CTGAGACAGG AGAATCACTT GAACCTGGGA GTTGGAGGCT 780
GCAGTGAGCC CTGATTGCCT CACTGCACTC CAGCCTGGGC CACAGAATGA TACCTGTCTC 840
AAAAAAAAAA AAAAAAAGTA GCAATAGCTA ACAACTATTG AATTATTGAG TGCCTACTAT 900
GTGCCAGACA CCATACTAAG TGGATTAGAT GGATATTCCA CATATTCTTC CCAAGAACAT 960
TATGAGGCAG GCACTATTAT CATCCCTGTT TTTAAAATGA GGAAACTGAG GCTCAGAGAT 1020
GTTAAATAAC TTGCTAAGGG TCACTCAGAA AACTAGTAGT AGAGAAGGGT TTGAATGCTG 1080
GCAGCCTGAC TCCAAGGCTC ATGTGCTTGC CTACCTTACC CAGATGGCGG CAGCACTGAG 1140
CAAGGGGTAG ATAACTTCAA GTCCCCTGGA AGAATAAGAG AAAGTGAGAC CATGGGGTAT 1200
GAGGGGGGCA GGCCCTGAGT AAAGCTTTAA AGGAGCAGTT GAAATTAGAC CCGGTGCCTT 1260
TGTTTAAGTA AGAAGAATGT GCTAGTTCTA AACAGATGCA GCCCCATACT GGGACTCACA 1320
GCTTGATGAG AAGCGCACTG GATGCATTTC AGCCCTTACT GCAACCTCAG CCTGAGGCCT 1380
TTATGCAGTG AGCAACCTGC ACAACCATAC ATAGCAATGT GAGTTTGATG GGAGAAGGAA 1440
GACCAGTGCA GAGACAAGGA TGTCGATGGA GTGCTTAGAG AACAAAGGGA AGCTATTTAC 1500
TAAAGCATGT TTGCATGGTG CAGGTGATTT TCTAAAGTTA ATTTTGACAG ACAGGATGGG 1560
GAAAGATTGT TGAAGGCCTG AAATGACAAG AGAGACTTGA GTGGATCTGG GAGGTCATGT 1620
GACAAACATG ACATTAACAA ATTCTAAATG GAAAAAATGA CCCTCAGAAA GTTGTGTGTC 1680
AAGGCCGGGT ATGGTGGCTC ACGTCTGTAA TTCCAGCACT TTCGGAGGCC AAGGCAGGTG 1740
GATCATTAGA GGTCAGGAAT TCAAGATGAG CCTGGCCAAC ATGGTGAAAC TCCATCTCTA 1800
GTAAAAATAC AAAAATTAGC CAGGCGTGGT GGCGGGCACC TGTAATCCCA GCTCCTCAGG 1860
AGGCTGAGGC AGGAGAATCT CTTGAGCCTG GGAGGCGAAT GTTTCAGTGA GCCAAGATTG 1920
CGCCACTGCA CTCCAACCTG AGCAACAGAG CGAGACCCTG TCTCGAAAAA AAAAAAAAGA 1980
AAAGAAAGAA AGTTGTGTGT CAAAAGCTTC AACACACAGG GGCCTTTGCT CTGTCAAGCA 2040
AGGAGAATAG GGTGGAGGAG GAACAGGAAC ACAGTAGCTA AGGTGACAGC TGCCTCACAA 2100
AAGGAAAGTC TATGGCTTGC AAAAGAGGTC GAGGAAAGCG GAAAAGCAAT TGCCGAAGAG 2160
GGACAGTAAG TGAAAAGATG AGTTTCTTCC ACTTGGCATC TCCCCAAATA TGGCCCTGAA 2220
GGAAGAGTTG ACCCTGTTAC GGTTTCTTTC TTTTTCCTGT GGGGTTATTA GAGTGACATA 2280
TAAGAAAAGG GCCACAGGCA CGGCACAGCT TGATTTCAGC CAGGCTTTGC ATGACACCCT 2340
ACAGAGCAGA ATGAGGACAG ATAGGCTGAA GGATAACTAC TTAACTGGGT AGGTTTCAAG 2400
TTGATACTCA GAGTGTTGAT TAAAGGGTGG TCAATGACAA CCTGGAGGAG GTCTTTAGGT 2460
AAAGAAACTG AGTTCAAAGA TAACCAACTT GCATGAATGA AGGAGCCAGG ATTTGAACCC 2520
AGCCCTACCT GATTCAAAAG TCCATTTTCC ATTTATTATA AAACAAAAAC CAAAAAGGCA 2580
TGAAGTTCAC TTATGAAAGA AGAGTTGAAA GATATAACCA GAGGGTTAGG AGTACAAATC 2640
CATGCCCGAA TGAATTGTGA TAGGCTGAGA AATTGGCCAA AGGGGGAGAA CAAAAACACA 2700
GTGAAAGTCA GAAAGGTTAA ATGTGAAGCC CTGCATTTTG GTTTCAAGAA ACCCGTTGCA 2760
GAGGTGGAGA 2770
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