EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS148-00385 
Organism
Homo sapiens 
Tissue/cell
NHLF 
Coordinate
chr1:43401830-43402890 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:43402790-43402808TCTTCCTTCCCTGCTCCC-6.18
ZNF263MA0528.1chr1:43402781-43402802CCCTCTCCCTCTTCCTTCCCT-6.31
ZNF263MA0528.1chr1:43402786-43402807TCCCTCTTCCTTCCCTGCTCC-6.9
Number of super-enhancer constituents: 43             
IDCoordinateTissue/cell
SE_01795chr1:43401101-43403350Aorta
SE_02447chr1:43401761-43403049Astrocytes
SE_04284chr1:43399877-43402347Brain_Anterior_Caudate
SE_05390chr1:43400269-43403582Brain_Cingulate_Gyrus
SE_06192chr1:43395065-43405505Brain_Hippocampus_Middle
SE_07319chr1:43400813-43402381Brain_Hippocampus_Middle_150
SE_08269chr1:43400734-43404931Brain_Inferior_Temporal_Lobe
SE_10377chr1:43396392-43405534CD19_Primary
SE_11009chr1:43387831-43425728CD20
SE_12470chr1:43400220-43403900CD3
SE_12760chr1:43401848-43401985CD34_fetal
SE_13825chr1:43401464-43405153CD34_Primary_RO01536
SE_14471chr1:43395753-43414527CD4_Memory_Primary_7pool
SE_19657chr1:43396427-43405202CD4p_CD25-_Il17p_PMAstim_Th17
SE_20345chr1:43395492-43405550CD56
SE_20799chr1:43396312-43405729CD8_Memory_7pool
SE_22754chr1:43395674-43405513CD8_primiary
SE_23189chr1:43399749-43406265Colon_Crypt_1
SE_23904chr1:43401192-43405387Colon_Crypt_2
SE_25177chr1:43399941-43405213Colon_Crypt_3
SE_26580chr1:43395721-43413249Esophagus
SE_29267chr1:43400819-43410293Fetal_Intestine_Large
SE_31882chr1:43401274-43405435Gastric
SE_33837chr1:43401475-43412846HCC1954
SE_34353chr1:43395339-43412997HCT-116
SE_35049chr1:43400682-43411164HeLa
SE_36013chr1:43400628-43405505HMEC
SE_37191chr1:43401608-43403612HSMMtube
SE_39883chr1:43397369-43405479K562
SE_42796chr1:43401554-43405089Lung
SE_50202chr1:43396219-43406255Sigmoid_Colon
SE_54088chr1:43400594-43405374Spleen
SE_55340chr1:43401594-43402708Thymus
SE_55821chr1:43399761-43405450u87
SE_57045chr1:43396858-43405413VACO_400
SE_58269chr1:43401710-43402795VACO_9m
SE_58561chr1:43388242-43430420Ly1
SE_60624chr1:43388552-43428820DHL6
SE_62392chr1:43388423-43425814Tonsil
SE_64094chr1:43401625-43404135HSMM
SE_64340chr1:43397259-43405516NHEK
SE_67781chr1:43399761-43405450u87
SE_68708chr1:43401621-43403290H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14340221443402581
Number: 1             
IDChromosomeStartEnd
GH01I042929chr14339554143414526
Enhancer Sequence
CCCCAGCAGG GATCCCTGGG CCAGGTTTAG GCTCGGTCTC AACTCTCCCT GTGCTCTACG 60
GGATGCTATT GTGGGGAAGA AGGGGCTAAA CTGCCAGCCA AGCTTTCAGC GCCAGTTACA 120
AGGAGGAAAG GGCCAGCTTC TCCGGCTTAG CCTCTCAGCC TGGCCTTCAC CCCTGTTCCT 180
TGCCTGCCCC TGTCTTCCAG TTGGGGCTGG CCCCACACTG CCCTTCCCAC AAGCTCTCAG 240
CCCAGGGCCT TCATCTCCAC AGCAACTCTC AGCCACACCC CAGGGTGAGC TGGGAGATTG 300
GAGCCAGATG TTCCAGGTGG GGCTGGACAG ATAACCCTGC CCACTGGGTC CCCTGGGGCC 360
TCACTTTGGG GCCTGGGGGA AGAGGCCCAG GTTGGGGCTA GAGCTGGGCC CCAACCCCCC 420
TGCAGAGGGC TGGACCACCC AGGCTGCTTC CCTGGAACAG CCCTGACATG GCTAGCCTCC 480
AAACCAAGGC CAGGCCAGGC CAGGCCTCCC GGTAGACAGA GGAATCATCC CACTGCCGTG 540
GCCACACCCG AAGCCCTTCT CAGCTCTTGC AATAAAGTGT CTCCTCTACC CCAACTATGA 600
CTCACAAGGC ACACGCAGTG ACTCCCTCAT ACGACCTAGA CACCTCACAC CTTTGCTTGG 660
GCCTAATCAC CTTTCAGAAC ATGCACAGAT ACTCCTCTGG AAAGCCTTCC TCCCGAGAAC 720
CACCCCTCCC ACTCCACTGC AACTGGTTCT CAAACAGAGA CGGCTTTGGT ACCCCATAGG 780
ACATCTGCCA ATGCCCAGAG ACATTTTTGG TTGCCACACT GGCTACTGGT ATCTAGAGGG 840
CAGAAGCCAA GGATGCTGAT AAACATCCTC CAATGCATGG GACAGGCCTC TACAACACCA 900
GCAGAAACAT CACAGTGCCA AGCTGAGAAA CCCTGCTCTA AGGGCGAAGC ACCCTCTCCC 960
TCTTCCTTCC CTGCTCCCAC TGTGCTTGCT CGCATTTCCA TCATCGCCTT TAGAAGACTA 1020
ACTGTAAGGT ACCGTGTGCT CCCTGTACAG TAAACCTCAG 1060