EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS187-16275 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr22:36849790-36852310 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr22:36851322-36851332GGGGCGGGGC-6.02
NRF1MA0506.1chr22:36851043-36851054GCGCCTGCGCA+6.62
Nr2f6(var.2)MA0728.1chr22:36850465-36850480GAGGTCAGGAGTTCA+6.22
SP1MA0079.4chr22:36851178-36851193GAGGGGCGTGGCTTT-6.58
SP4MA0685.1chr22:36851176-36851193CGGAGGGGCGTGGCTTT-6.25
SRFMA0083.3chr22:36851292-36851308TCGCCTTATATGGGCA+6.1
SRFMA0083.3chr22:36851292-36851308TCGCCTTATATGGGCA-6.71
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_01080chr22:36850726-36852262Adrenal_Gland
SE_01722chr22:36849761-36850518Aorta
SE_01722chr22:36850607-36852913Aorta
SE_23071chr22:36849767-36850476Colon_Crypt_1
SE_23071chr22:36850671-36852560Colon_Crypt_1
SE_23740chr22:36849892-36850455Colon_Crypt_2
SE_23740chr22:36850718-36852282Colon_Crypt_2
SE_24731chr22:36849795-36850420Colon_Crypt_3
SE_24731chr22:36850718-36852420Colon_Crypt_3
SE_26443chr22:36850607-36852611Duodenum_Smooth_Muscle
SE_27096chr22:36849818-36850504Esophagus
SE_27096chr22:36850705-36852669Esophagus
SE_27650chr22:36849724-36850464Fetal_Intestine
SE_27650chr22:36850647-36852400Fetal_Intestine
SE_31378chr22:36846951-36850494Gastric
SE_31378chr22:36850633-36852734Gastric
SE_38695chr22:36850357-36852234HUVEC
SE_40577chr22:36850636-36852007K562
SE_41064chr22:36850677-36852892Left_Ventricle
SE_42094chr22:36849674-36850508Lung
SE_42094chr22:36850596-36852908Lung
SE_47671chr22:36849971-36850303Pancreas
SE_47671chr22:36850712-36852254Pancreas
SE_49127chr22:36850680-36852736Right_Atrium
SE_49784chr22:36850757-36851955Right_Ventricle
SE_50050chr22:36846927-36850521Sigmoid_Colon
SE_50050chr22:36850646-36852826Sigmoid_Colon
SE_51467chr22:36849566-36852911Skeletal_Muscle
SE_52340chr22:36849797-36850508Small_Intestine
SE_52340chr22:36850703-36852749Small_Intestine
SE_53283chr22:36846840-36850510Spleen
SE_53283chr22:36850603-36852908Spleen
SE_54687chr22:36849576-36855238Stomach_Smooth_Muscle
SE_55607chr22:36849875-36850439Thymus
SE_55607chr22:36850710-36852282Thymus
SE_57815chr22:36850729-36851204VACO_503
SE_57815chr22:36851243-36851946VACO_503
SE_62151chr22:36773097-36852649Toledo
SE_63127chr22:36801020-36866853Tonsil
SE_65459chr22:36849505-36852516Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr223685160036852198
Enhancer Sequence
CTGGCCAAGC TGGTCTCGAA CTCCTGACCT CAAGTGATCC TCCTGCCTCG GCCTCCCAAA 60
GTCCTGGGAT TACAGGTGTG AGCCACCGCG CCAGGCCGGT AGGAGGGTTT AAACAGGAAA 120
GAGATAAGCA GTCAGATTCA TAGTTTAGAA AATCCTCAGG TTCTGGTGTT CGGGTGGATG 180
CCTGGAGTGG GGATCTGGAA ATCAGGGGCA GGGGTTAGTA ATAACCCAGG TGAGGAGACT 240
TGAGTCTAGA GGCAGCCAAG TGGGGACCTA TGGAGGAGTT CACGTGCTGC AGGTGTGCGC 300
CGCCGAGGCG GAGCCAGGCT CTGGAGCTGC CAGGGGCTCA GAAGCCTCCC TCTCAGATCT 360
CTCCCCTTTT GGCCACAGAT GGGAAGGAGA GAGGCACTCA CCCGACCCAG CGTGGCAGTA 420
CAGTAGTGTC CAACCTGTCA CTGTTGGGCG TGGTGGCGTG TACCTGTAGT CCCAGCTACT 480
GAGGAGGCTG AGATGGCAGC AGCACTTGAG CCCAGGAGTT GGAGGCTGCA GTGAGCCGAC 540
AGCGCCACTG AACTCTAGCC TGGGTGACAG AGCGAGACCC TGTCTCTAAA AAACAGAAAA 600
GAAAAATTAC AGGTCGGGCG CAGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGCCG 660
AGGAGGGTGG ATCACGAGGT CAGGAGTTCA AGACCAGCCT GGCCAATATG GCGAAACCCC 720
GTCTCTACTA AAAATACAAA AATTAGCCAG GCGTGGTGGT GTGCGCCTGT AGTTTCAGCT 780
ACTTGGGAGG CTGAGGCAGG AGAATAGCTT GAACCCGGGA GGCGGAGGTT GCAGTGAGCC 840
GAGATCACGC CACTGCACTC CAGCCTGGCA ACAGAGCGAG ACTCTGTCTC AAAAAAAAAA 900
AAAAAAAAAA AAAAAAAAGA AAAAGAAGAA AAAGAAAAAA GAGAAAGAAG GAAAGAATTA 960
CATAACAGTA AGCAACCTAG CTAGATTTGA ACCAGGCCCT GCAGTTCTAA AGCACTGGCT 1020
TTTGCGGAGC GGCACTCACT CCGCATCGTG GCATAGGTAG ATTTCTTTTC TAAAGGTGAG 1080
GTCAGTGCTG GGCACTTAGC AGGCGCCCGG TGGGCTGCGC CGTCCTGGAG GAAGGCTGAT 1140
TCCTCCCACC CCGACTCCTG GCTCGTGGGT GGGTAATCCA GCACATTCTC CCCACCCCGG 1200
CAACCAACTT TGTGGCCGAA CAAGCCCTCC CCGGCTTGTT CCGCTGGTCC CAGGCGCCTG 1260
CGCATCCGGA CACGATGAGG AGCAGGTGCG CGGGGCCGGG GTGTGTTCGA GGGGGTCGTG 1320
CGCGCCTGGG CTGCCTCCCC GCGGACGGCG GACTGGGCCG GGGCGGCGCT TCCTGGCAGA 1380
GAGGCGCGGA GGGGCGTGGC TTTGGAGAGG TGCCCCCGGC GGGCTGGCGG CCTGGCTGCG 1440
GTGAAAGGCG GGCGGACGCA GGTGACGACA ACCGCTCCAT AAAGGGCGCC GCGGCGCGAC 1500
GCTCGCCTTA TATGGGCAGG CTCGGCGCGG GAGGGGCGGG GCGTTCCACC CAGCTGGCTC 1560
CGCACCGAGG CCCGGCCGAA CCCCCGAGGG GGGAAACTTC TCTGCGAGGG TGGAGCCTCC 1620
TCAGCGGCGT CCCCAGGTCC CGAGAGGGGT CCCTACCCAG GCTAAGACTC ACGACGGGCT 1680
CCACCCTGCA GGGGCTCAAC TTGCAGAAAC CCTGGGGCCT GCCTTCCCCA GGGGTCTGCC 1740
CTCCTCAGGC CCTGCTAGGG CACTGACTCG GTTTGTGCTG TGTGGCGTTT TTTCCTTCAC 1800
CCCACCTGGG CCGCAGGTCC TCGCTAGATA GCCGAGGGAG GGTCCTTTAA GTGAGCTCAC 1860
CTCGGAGCCC CCAGATAACC AAGCCTGAGC CTCCCGGCTA CATGGCGAGG CTTCCCCAAT 1920
CCGGTCAGCC CCAAGCAGGT GCCTTTCTCT AACTGGCACA AAGGAAGTCT CCTAGCCAGG 1980
CTGAGCCCAA GCCTCGGTAA ACATGAGCCT TGGATCCACT GGAAGTGTTT GGCTAACTGG 2040
GCCCTTCTTG GCCAGACAAG ACTTTAACCC TAAGAGGAAG CTGCCAGCAT GACGCAGCCC 2100
ACCATATTCT CCCTCCAAGC TCTCTTCATA GCCCGGGTCC TTAAAAACCC AAATCTGTCC 2160
AATTGCTACT TGCCGTCCAC TCGTTGACAG TTACTCCGCT TCACAGCCTC CCGATCACCT 2220
GAGTGTCCTC CCTCGGCTCA GTGCACAGGG CTCTGTGAGC TTACAGTTCC CTGGTTGCCG 2280
TTCCGTGCCT CCCAGCCCTG CACCTGCTGC TCCTTTCTGG AAAGCCCTTT CCTTGCACAC 2340
TCCCAGACAC GTGCTCACCC TTCAGAGAGA TACTTCTTAG CGTCTTCTTC CTGACATTTG 2400
TAGTGATTAC TTAACCTTTC TGAGCATCAA TTTCTTCATC TGCAAGATGG GGGTAAAATA 2460
ATCCCCACCT CACTGTGTTA TTGTGAGGAT CGAATGAGTT AATGTTTGTA AAATGCCTGG 2520