EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS180-50252 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr9:130722310-130723860 
Number of super-enhancer constituents: 45             
IDCoordinateTissue/cell
SE_00925chr9:130722340-130724569Adrenal_Gland
SE_03057chr9:130722531-130723370Bladder
SE_03199chr9:130722248-130723760Brain_Angular_Gyrus
SE_03920chr9:130722122-130743170Brain_Anterior_Caudate
SE_04847chr9:130721221-130743183Brain_Cingulate_Gyrus
SE_05831chr9:130721845-130743215Brain_Hippocampus_Middle
SE_06733chr9:130721287-130743210Brain_Hippocampus_Middle_150
SE_07809chr9:130720890-130743184Brain_Inferior_Temporal_Lobe
SE_08813chr9:130722454-130722653Brain_Mid_Frontal_Lobe
SE_08813chr9:130722880-130723128Brain_Mid_Frontal_Lobe
SE_08813chr9:130723312-130723509Brain_Mid_Frontal_Lobe
SE_11447chr9:130720866-130724419CD20
SE_14569chr9:130722204-130724217CD4_Memory_Primary_7pool
SE_17435chr9:130709572-130746682CD4p_CD25-_CD45RAp_Naive
SE_18002chr9:130720768-130744821CD4p_CD25-_CD45ROp_Memory
SE_18414chr9:130710005-130746664CD4p_CD25-_Il17-_PMAstim_Th
SE_19352chr9:130721013-130724025CD4p_CD25-_Il17p_PMAstim_Th17
SE_23098chr9:130722295-130724452Colon_Crypt_1
SE_23795chr9:130722314-130723877Colon_Crypt_2
SE_24877chr9:130722278-130723927Colon_Crypt_3
SE_26056chr9:130721918-130723628Duodenum_Smooth_Muscle
SE_26592chr9:130721630-130727290Esophagus
SE_27793chr9:130722039-130723892Fetal_Intestine
SE_28855chr9:130722033-130723899Fetal_Intestine_Large
SE_31068chr9:130722225-130724122Fetal_Thymus
SE_31463chr9:130722233-130724035Gastric
SE_33464chr9:130722193-130724208H2171
SE_35074chr9:130722319-130724054HeLa
SE_40859chr9:130722238-130723680Left_Ventricle
SE_41564chr9:130722309-130724482LNCaP
SE_42441chr9:130722277-130724003Lung
SE_47183chr9:130721861-130742929Panc1
SE_47513chr9:130722336-130722572Pancreas
SE_47513chr9:130722664-130723031Pancreas
SE_48807chr9:130722238-130723941Right_Atrium
SE_50126chr9:130722211-130724478Sigmoid_Colon
SE_52385chr9:130722251-130727314Small_Intestine
SE_55082chr9:130722473-130723693Stomach_Smooth_Muscle
SE_55220chr9:130722244-130723539Thymus
SE_58224chr9:130722357-130723658VACO_9m
SE_60506chr9:130716304-130754833DHL6
SE_62382chr9:130716187-130753973Tonsil
SE_63200chr9:130716389-130744141GLC16
SE_65295chr9:130722004-130743108Pancreatic_islets
SE_68948chr9:130722256-130725184H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9130722674130723273
Number: 1             
IDChromosomeStartEnd
GH09I127959chr9130722115130724119
Enhancer Sequence
AAGCTGTTAA ATACATGGTA GGTCAGATAA ATAGAAAAAT GGAGAACACC ACAGGGAAGG 60
TGTGTGGGGA GTGCAGGTAG CGATGAGGTG TGGCTGCTTC AGGTGGGGGG TTAGGGATGG 120
CCCTTAGGGC AGTGACATCT GAGCACGGCT TGGACTGAAG TGGGGACTGA GCAAAGACAG 180
GGGAAGAGCC CTCCAGGTGA GGGAGCAGCA AGTGCAGAGG CCCTGAGGCA GAAACACACT 240
TGGCAGGTAG AAAACTAGTG CAGAGGACAG TGGCTGAAGA GGAGCTGGGG GGAGATCAGA 300
GGGGATGAGA TGGGTGAAGG AGCAGGGGCA GGTCCTGCTA GACCTCAAGG GTGTGAGAAG 360
ACTGCATCTG ATTCTGACAG CGGCTCTGTC TTGCCCCCGT GGACTGTGGC TTAGGCAGAG 420
GCTGAGAACA GCCACAGAGG AGGAGAATGG AAGGGCAAAG AGAGCAGAGA CACTTCCCAG 480
GCAGCCAGAG GAGGCCCAAG CTTGAAAGGG GGAAGGCTGG GGAGTGGCCA TGGCTCCCCA 540
CACTTCACCT AGGGTTGGAA GCAGCTGCTG GAGGCCTGGG GAGGCAGCTC GGTGCTCTGG 600
GCATGTTGAA ACACCCAGTG GAATTGGGAT TAGTGTCTGG GAACAAAAGC TCACAGTGAA 660
TTGTGGGCTT TCTCCCTTTC CTTTTGAGAG TTTGCTGTGG GAACGCCAGC CAGGAAGCCT 720
AAGGCCCATT TGCAGTTCCA GGGCCAAGCC AGAAAAAGCC ACCTGGAACC CTCCTAGCTC 780
AGGTAACAGG CACATTCCCC CCTCCACAGG AAGAGCTCAC AGGGTCAGCA CTGGGCCTCC 840
CTCCTGTTTC TACAGGGCTC TGAACAATCA CCTATTGGAA GCCACCACTC CCACGGGAAG 900
AGGCAAGCAG CCTCGCCCTG GCCCACGGCC AGAGGTCACA GCAAGGGTAA AAAAAAAACC 960
ACAGCAGCAG CGGCCACCTC CTGAGGGCCT ACTGTGTGCG GCCCAGAACT CTTCAACACT 1020
GAAAGGTGAC TGCTACCACA GCCCACTTTA CAGATGGGGA AAGTGAGGCT CAGAAATGCT 1080
GCGTAACTCA TCTGAAGTCA CAGCAGAGCT AGTCTCGACC CCAGCCCCAT CTGCGTCCAG 1140
ACCCTGTGTC ACAGCTGGGA CACAGCTATG CAGCTGCCTC AGGGCCCACA CTGCCTCCCC 1200
CTCAGCCCCG GGGCCCCTCT GGTGGGAAGC AGCTGGGCAC CCCCAGGCAG GTGGCATGCA 1260
TGGGGCATGA TCCCATGCAT GGGGCAGGGA TCATGGTGGG AGATGAACAC AGGCTCAGGC 1320
AGGGTGGGGT AAGGGATGCT TGTGATGGGA GGTGGGAATG AGGATGCCAG GCAGGCAGCC 1380
ATGAGCCCCA GGTTGGGAGC TGGCCAGGTC AGGACTGAGG ACATCTCAGA GCCTTGATCC 1440
ATTCAGAAAC CTTTTATGAA GCCCCCACCA GGTGCCAGGC ACTGCTGAAG GCTCTGGGAA 1500
CACAAGCAAT AAACAGAGAA GACAGAAATC CCTGCCTTCA AGGGGCTTAT 1550