EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS077-07761 
Organism
Homo sapiens 
Tissue/cell
H128 
Coordinate
chr22:36847100-36849520 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HES2MA0616.2chr22:36848303-36848313GGCACGTGCC+6.02
HES2MA0616.2chr22:36848303-36848313GGCACGTGCC-6.02
IRF1MA0050.2chr22:36847412-36847433AAAAAAAAAAAGAAAGAAAGA-6.25
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_01080chr22:36847242-36849040Adrenal_Gland
SE_01722chr22:36847032-36849110Aorta
SE_23071chr22:36847129-36848276Colon_Crypt_1
SE_23071chr22:36848327-36849168Colon_Crypt_1
SE_23071chr22:36849234-36849718Colon_Crypt_1
SE_23740chr22:36847151-36848263Colon_Crypt_2
SE_23740chr22:36848358-36849060Colon_Crypt_2
SE_24731chr22:36847121-36848298Colon_Crypt_3
SE_24731chr22:36848386-36849083Colon_Crypt_3
SE_26443chr22:36846973-36849379Duodenum_Smooth_Muscle
SE_27096chr22:36847046-36849682Esophagus
SE_27650chr22:36847131-36849159Fetal_Intestine
SE_31378chr22:36846951-36850494Gastric
SE_38695chr22:36847032-36848827HUVEC
SE_40577chr22:36847241-36848311K562
SE_41064chr22:36847075-36849166Left_Ventricle
SE_42094chr22:36847025-36849126Lung
SE_47671chr22:36847179-36847421Pancreas
SE_47671chr22:36847464-36847828Pancreas
SE_47671chr22:36847870-36848264Pancreas
SE_47671chr22:36848337-36849062Pancreas
SE_49127chr22:36847325-36849115Right_Atrium
SE_50050chr22:36846927-36850521Sigmoid_Colon
SE_51467chr22:36846973-36849359Skeletal_Muscle
SE_52340chr22:36847023-36849262Small_Intestine
SE_53283chr22:36846840-36850510Spleen
SE_54687chr22:36847186-36849303Stomach_Smooth_Muscle
SE_55607chr22:36847126-36848284Thymus
SE_55607chr22:36848319-36849125Thymus
SE_62151chr22:36773097-36852649Toledo
SE_63127chr22:36801020-36866853Tonsil
SE_65459chr22:36847035-36849068Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr223684783036847945
chr223684837336849008
Enhancer Sequence
TTCACCATGT TGCCCAGGCT GGTCTTGAAC TCCTGAGCTC TGGCAATCTG CCCACTTCGG 60
CCTCCCAAAC TGCTGGGATT ATAGGCGTGA GCCACCGTGC CTGGCCGCAA ATAAGGATTT 120
AATAATGACG ATGATAAAAT AGAAGGGAAA ATCTCAGAGC ACATCCTGGG TAGTAATAGC 180
AAACTGTCTT GGCTGTGTGG TGGCTCATGC CTCTAATCCC AGCATTTTAG GAGGCCAAGG 240
CAGGAGGACT GCTTGAGGCT AGGAGTTAAA ATCAGCCTAG GCAACACAGT GAGGCCCCAT 300
TCCTACAAAA AAAAAAAAAA AAAGAAAGAA AGAAAAAATT AGCCGGGTAT GGTGGTGTGT 360
GCCTATAGTC CTAGCTACTC CAGAGGCTGA GGCGGGAGGA TTGCTTGCGC CCAGGAGTTC 420
AAGGCTGCAG TGAGCCATGA TCGTGCCATG GTACGGCAGC CTGGGTGACA GAGCAAGGCC 480
CCAACTCTGA AAAACAAAAT AAATACAATA AAATAAAATG GTCAAAATGG CCTGGTGCAG 540
TGGCTGGTGC CTGCAACCAG AGCTACTTGA GAGGCTGAGG CAGGAGAATC ACTGGAGCCC 600
AGGAGGTTGA GGCACCACTG AACTCCAGCC TGGGTGAGAG TGAGATCCTG TCTCTTTAAA 660
AAAGAAAAAA CAAAAAAAGC AAACTGTCTC ATGAAACTCT TGTTTCCATG TTGCACGCTC 720
TGCCAGGTTG TGATGTAATG TATTTCTTAC TCTGGGTCAC AGTCACAAAA CCTTGAAATG 780
TCACTCACTG TCTTGGCTCA TGCGTCGTAA GCCTTTGTTC CCCAACAGGG GGAAGTGAAC 840
CAGCACACAA GGCCCTTCCG TCCTGCGGAG CTCACTGCCT TCCTCAGCTC CTGGCCCGCA 900
CTTCCGACCA CACACTGGGG ACACACCCTC GGGGGGGCCC CACCCCAGCA GCTGCCCATG 960
TTCACACCTC TTCAGTTATT TCAAACTCCG CCTCTCTCGG CCTGATGCCC AACACTTCCT 1020
TCACCCAAGG AGGTCCTGTT CAAATATCAC TTCTGGCCAG GCGCGGTGGC TCAGGTCTAT 1080
AATCCCAGCA CTTCGGGAGG CCCCGAGGCA GGCAGATCAC CTGAGGTCAG GAGTTTGAGA 1140
CCAGCCTGGC CAACAGGTGA AACCCCGTCT CTACTAAAAA TACAAAAATT AGCCAGGTGT 1200
GGTGGCACGT GCCTGTAGTC CCAGCTACTC AGGAGGCTGA AGCAGGAGAA TTGCTTGAAC 1260
CTGGGAAGCG GAGGTTGCAG TGAGCCAAGA TTGAGCCATT GCACTGCGGC GTGGGAGGCA 1320
GAGGTAGACT CTGTCTCAAA AAAAAAAAAA GTCACTTTCT CTGCCAGTCA TATCTTCTGC 1380
AACCCTGAGG AGCCAGGCAG GACGACCCCT TTACCCTCTG AATCAATTGG TCTGTATCAG 1440
GGTCTGGCAG AGGGAGGGGA AGTTGGCCCC TCTGATTTAA TGGATGAATC AAGAAAATGT 1500
GTGACTGAGC CATGGATTCA TGGGGATGGG GTCCTGGAGC AGAGGCTTGC TGTGCACCTA 1560
CTAGGTGCTG TGTACCTCAC AAGCCACTGG GGACATCAGA CCACCAGAAT AAGTCCACTT 1620
TCCCCAAGGA AAGTGGTCAA ATGTGGGAGC CAGGTGTGCA AATCCCCACC CCAGGGTGAT 1680
AACAGCCCCA ATAAAGGCAC ATGCAAGGGG GACCTTCGGA GCTGATGACA CTGTACAGGC 1740
ATCTAAGAGG CTGGTGACAG GGTCACCAAG CAGAGGTCTA GAGCAGGGCT GAGTGGGGTA 1800
GGGGGGGTTC TTCCAGGCAA AAGGCAAAAA CTCTGTTGGT ACCGTGTAGG TCTTCCACAG 1860
CACATGCCAC ATGAGAAGAA ACATTCGCCT GGCGAGTGGC TGAAGTCTAT AATCCCAGCA 1920
CTTTGGGAGG CTGAGGCAGG TGGATCGCTT GAGCCAAAGA GTTTGAGATC AGCCTGGGCA 1980
ACATGGCAAA ACCCCGTCTC TACAAAAAAT ACAAAAATTA GCCAGGTGTG GTAACCCATG 2040
CCTGTGGTCC CAGCTACTCG GGAGGCTGAG GTGGGAGGAT TGCTTAAGCC TAGGAGGTCA 2100
AGGCTGCAGT GAGCCATGAT TGTGCCACCA CACTCCAGCC TCAGTGACAG AGTGAGACCC 2160
TGTCTCGAAA AAAAAAAAAA AAAAAGAGAG GGAAAGGAAA AATTTTATTT TACATTTATG 2220
TATTGAGGGC AGGGACCATG CCTGCTGGGC TGCTCACCAC TGCTGAGCAG GATTCCTGGT 2280
GTGGCATCCT AACACAATAA ATATTTACTG AATGTGTACT CAGGAAACTG CAAAGGGTTC 2340
AGGCTGGCCT GAGAGTAAAG TGAAAGAAGG AAGTGGTAGA AGAGCCCAGA GGTCTGTGAC 2400
CCCAGAACCT GGAGGGCACC 2420