EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS065-03502 
Organism
Homo sapiens 
Tissue/cell
GM18508 
Coordinate
chr22:36775520-36776740 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Klf1MA0493.1chr22:36775759-36775770AGCCACACCCT+6.02
Number of super-enhancer constituents: 55             
IDCoordinateTissue/cell
SE_00116chr22:36773956-36778456Adipose_Nuclei
SE_00874chr22:36775464-36776417Adrenal_Gland
SE_01541chr22:36775080-36776624Aorta
SE_02243chr22:36775435-36776627Astrocytes
SE_02896chr22:36775545-36776452Bladder
SE_05865chr22:36775219-36777056Brain_Hippocampus_Middle
SE_06839chr22:36775434-36776598Brain_Hippocampus_Middle_150
SE_09195chr22:36774100-36778426CD14
SE_10697chr22:36771941-36778231CD19_Primary
SE_11020chr22:36744527-36785336CD20
SE_11868chr22:36770468-36776664CD3
SE_13866chr22:36774014-36777543CD34_Primary_RO01536
SE_14476chr22:36772133-36776938CD4_Memory_Primary_7pool
SE_15488chr22:36772160-36776567CD4_Memory_Primary_8pool
SE_15971chr22:36772104-36776422CD4_Naive_Primary_7pool
SE_16465chr22:36775208-36776718CD4_Naive_Primary_8pool
SE_16932chr22:36772150-36776632CD4p_CD225int_CD127p_Tmem
SE_17339chr22:36756664-36780212CD4p_CD25-_CD45RAp_Naive
SE_17788chr22:36746596-36785463CD4p_CD25-_CD45ROp_Memory
SE_18286chr22:36744506-36778586CD4p_CD25-_Il17-_PMAstim_Th
SE_19119chr22:36756666-36778387CD4p_CD25-_Il17p_PMAstim_Th17
SE_20220chr22:36770449-36776653CD56
SE_20975chr22:36772185-36776575CD8_Memory_7pool
SE_21488chr22:36772140-36776693CD8_Naive_7pool
SE_21957chr22:36771955-36776719CD8_Naive_8pool
SE_22328chr22:36770356-36778565CD8_primiary
SE_23071chr22:36775515-36776329Colon_Crypt_1
SE_23740chr22:36775535-36776459Colon_Crypt_2
SE_24731chr22:36775546-36776521Colon_Crypt_3
SE_25782chr22:36772682-36776457Duodenum_Smooth_Muscle
SE_26521chr22:36775459-36776581Esophagus
SE_30956chr22:36775430-36776628Fetal_Thymus
SE_31378chr22:36775480-36776618Gastric
SE_35832chr22:36775421-36776107HMEC
SE_37948chr22:36772124-36777315HUVEC
SE_40597chr22:36775441-36776642Left_Ventricle
SE_42094chr22:36775432-36776618Lung
SE_44762chr22:36775551-36776201NHLF
SE_45604chr22:36774033-36776672Osteoblasts
SE_47169chr22:36775624-36776708Panc1
SE_47463chr22:36775631-36775945Pancreas
SE_48566chr22:36775474-36776614Right_Atrium
SE_50050chr22:36775440-36776623Sigmoid_Colon
SE_51217chr22:36775254-36776632Skeletal_Muscle
SE_52340chr22:36775469-36776608Small_Intestine
SE_53283chr22:36775444-36776646Spleen
SE_54489chr22:36773951-36777410Stomach_Smooth_Muscle
SE_55183chr22:36775500-36776535Thymus
SE_55761chr22:36775538-36776393u87
SE_58448chr22:36724049-36832686Ly1
SE_62151chr22:36773097-36852649Toledo
SE_62244chr22:36719186-36785326Tonsil
SE_65307chr22:36775072-36776722Pancreatic_islets
SE_67526chr22:36775538-36776393u87
SE_68689chr22:36775418-36776641H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr223677554436776466
Enhancer Sequence
TCCAGCCTGG GTGACAGAGC GAGACTCCGT CTCAGAAAAA TAAAAAGTTG TACAGAAAGA 60
CATCATCTTG GCCTAAGAAG GCAAGAGAGG GACCTCCCTG AGAAGCCCCT TTTCTCCTCT 120
GGGACATACC ATAAGGATGG TAAGGGCCTC TGAGAAGTAC CAAGGAAGTG ACTCGAGGGT 180
GGGGAAGATC AGCTACCTGT AACCCCACTA CAGGCCTTAG CCCAACCTGC ACGGCAGGAA 240
GCCACACCCT TCCGGAAGGC CCTGCAAAGG CTCCTTCCAG CCACAGCAGG AGGGTCCTGG 300
GCTAGAGATG CAGACAGCCA CTGAGGGACT CCCAGCTGCT CCAGCGCTTG GCGGGCTAGC 360
TAAGGGCCTT CTCTGGGGAC ACCTGCCCGG GTGCTGAATC ATCTCAGGCT CGAGAAGCTA 420
ATCGTGGGAA TGGGAACCTG AGTAATTCCA ACAGAAGCCT AGGTTACTTT TTAAAGAGAC 480
ATGCATCAGA GTGGGCAGCT CCCCTCCTGC CTCCCAAATA TTTGGTGCCA TCTAAGCACA 540
AGGGACAGGG AGCTGGGTAC AGATACAGGC CGCCCGCCCA TGCAGTGGCG GTCCCATTTT 600
AGAGCCAGTC TCATAGTGTG TGCTCATGTG TGACTCACAC CATTCCCCCA GGAGGCCCGG 660
AGGCTGCCTT GCAGGACCTC AGGACCCTGA TGGGGTCTTC CAGACTTCAC TCAGGAAAGG 720
AGTCAATCGG GCACAACAGC AGCGCCGGCA GCTCCTCCCA GGGCCCACAC CATCCAAGGC 780
GAAAGACAGC CATCCTTGAG AAGGGGGGTA GGGCCCTCCC ATTCAAAACA CCCCTCTGAT 840
CACATCTTCT CAAGAATTTG GGCTTTTCCA GTGTTGTTAT ACATAAAAAC CACAGGCCAG 900
ATGTCTTAGG GGAAACTGGG GACAGAGTGG GAAGGGGCAT AATAGTGGAT GCAATGACCC 960
CAAGTTAAAA AAGAAGGCCA GGTGGCCGGG TGCGGTGGCT CACGCCTGTA ATCCCACCAC 1020
TTCGGGAGGC CAAGCCAGGT GGATCACCTG AGGTCAGGAG TTCGAGACCA GCCTGGCCAA 1080
CATGGTGAAA CCCTGCCTCT ACTAAAAATA CAAAAATTAG CCAGGCGTGG TGACAGGTGC 1140
CTATAATCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATC GCTTGAACCT GGGAGGTGGA 1200
GGTTGCAGTG AGCTAAGATC 1220